paragraph_index int64 | sec string | p_has_citation int64 | cites string | citeids list | pmid int64 | cited_id string | sentences string | all_sent_cites list | sent_len int64 | sentence_batch_index int64 | sent_has_citation float64 | qc_fail bool | cited_sentence string | cites_in_sentence list | cln_sentence string | is_cap bool | is_alpha bool | ends_wp bool | cit_qc bool | lgtm bool | __index_level_0__ int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5 | DISCUSSION | 0 | null | null | 16,157,683 | null | That a normally sublethal pathogen dose imparts 60% mortality in IL-23 p19−/− animals confirms the critical requirement for this cytokine in surviving pulmonary K. pneumoniae infection. | null | 185 | 43,119 | 0 | false | null | null | That a normally sublethal pathogen dose imparts 60% mortality in IL-23 p19−/− animals confirms the critical requirement for this cytokine in surviving pulmonary K. pneumoniae infection. | true | true | true | true | true | 7,466 |
5 | DISCUSSION | 0 | null | null | 16,157,683 | null | Bacterial clearance could be significantly enhanced in IL-23 p19−/− mice by administration of recombinant IL-17 at 12 h into the infection, and this treatment restored G-CSF and LIX production without correcting IL-6 expression. | null | 228 | 43,120 | 0 | false | null | null | Bacterial clearance could be significantly enhanced in IL-23 p19−/− mice by administration of recombinant IL-17 at 12 h into the infection, and this treatment restored G-CSF and LIX production without correcting IL-6 expression. | true | true | true | true | true | 7,466 |
5 | DISCUSSION | 0 | null | null | 16,157,683 | null | These data suggest that the absence of IL-17 signaling in p19−/− mice mediates the observed phenotype and that IL-17–induced IL-6 signaling is not a critical component of host defense in this infection model. | null | 208 | 43,121 | 0 | false | null | null | These data suggest that the absence of IL-17 signaling in p19−/− mice mediates the observed phenotype and that IL-17–induced IL-6 signaling is not a critical component of host defense in this infection model. | true | true | true | true | true | 7,466 |
5 | DISCUSSION | 0 | null | null | 16,157,683 | null | Despite the absence of IL-12 and markedly diminished lung IFN-γ induction in IL-12/23 p40−/− mice, IL-17 treatment still reduced significantly the high bacterial burden observed in these mice, further suggesting IL-17 plays a significant role in host defenses in this model independent of IL-12/IFN-γ signaling. | null | 311 | 43,122 | 0 | false | null | null | Despite the absence of IL-12 and markedly diminished lung IFN-γ induction in IL-12/23 p40−/− mice, IL-17 treatment still reduced significantly the high bacterial burden observed in these mice, further suggesting IL-17 plays a significant role in host defenses in this model independent of IL-12/IFN-γ signaling. | true | true | true | true | true | 7,466 |
6 | DISCUSSION | 1 | 40 | [
"bib40",
"bib41",
"bib43"
] | 16,157,683 | pmid-12077275|pmid-12624114|pmid-14720045 | We recognize that the current study has important limitations. | [
"40",
"41",
"43"
] | 62 | 43,123 | 0 | false | We recognize that the current study has important limitations. | [] | We recognize that the current study has important limitations. | true | true | true | true | true | 7,467 |
6 | DISCUSSION | 1 | 40 | [
"bib40",
"bib41",
"bib43"
] | 16,157,683 | pmid-12077275|pmid-12624114|pmid-14720045 | Namely, we have not identified the specific effector immune functions defective in the absence of IL-23 signaling. | [
"40",
"41",
"43"
] | 114 | 43,124 | 0 | false | Namely, we have not identified the specific effector immune functions defective in the absence of IL-23 signaling. | [] | Namely, we have not identified the specific effector immune functions defective in the absence of IL-23 signaling. | true | true | true | true | true | 7,467 |
6 | DISCUSSION | 1 | 40 | [
"bib40",
"bib41",
"bib43"
] | 16,157,683 | pmid-12077275|pmid-12624114|pmid-14720045 | Because IL-17 and IL-17F elicit neutrophil recruitment in the lung (40), defects in the number or function of these cells may also underlie the observed phenotype. | [
"40",
"41",
"43"
] | 163 | 43,125 | 1 | false | Because IL-17 and IL-17F elicit neutrophil recruitment in the lung, defects in the number or function of these cells may also underlie the observed phenotype. | [
"40"
] | Because IL-17 and IL-17F elicit neutrophil recruitment in the lung, defects in the number or function of these cells may also underlie the observed phenotype. | true | true | true | true | true | 7,467 |
6 | DISCUSSION | 1 | 40 | [
"bib40",
"bib41",
"bib43"
] | 16,157,683 | pmid-12077275|pmid-12624114|pmid-14720045 | Impaired antimicrobial peptide production may also contribute to enhanced mortality, as IL-17 signaling has also been shown to induce airway epithelial cell expression of mucin and β defensin 2 proteins, molecules important in bacterial clearance (41–43). | [
"40",
"41",
"43"
] | 255 | 43,126 | 0 | false | Impaired antimicrobial peptide production may also contribute to enhanced mortality, as IL-17 signaling has also been shown to induce airway epithelial cell expression of mucin and β defensin 2 proteins, molecules important in bacterial clearance. | [
"41–43"
] | Impaired antimicrobial peptide production may also contribute to enhanced mortality, as IL-17 signaling has also been shown to induce airway epithelial cell expression of mucin and β defensin 2 proteins, molecules important in bacterial clearance. | true | true | true | true | true | 7,467 |
7 | DISCUSSION | 1 | 44 | [
"bib44",
"bib46",
"bib47"
] | 16,157,683 | pmid-9206995|pmid-8245795|pmid-15657292 | Our data support a critical role for IL-23 and IL-17 in early host resistance to K. pneumoniae independent of IL-12 and IFN-γ. | [
"44",
"46",
"47"
] | 126 | 43,127 | 0 | false | Our data support a critical role for IL-23 and IL-17 in early host resistance to K. pneumoniae independent of IL-12 and IFN-γ. | [] | Our data support a critical role for IL-23 and IL-17 in early host resistance to K. pneumoniae independent of IL-12 and IFN-γ. | true | true | true | true | true | 7,468 |
7 | DISCUSSION | 1 | 44 | [
"bib44",
"bib46",
"bib47"
] | 16,157,683 | pmid-9206995|pmid-8245795|pmid-15657292 | It is possible that IL-23 and the subsequent IL-17 pathway have evolved to handle extracellular gram-negative bacterial challenges, because IL-17 is not required for host resistance against intracellular organisms such as Listeria monocytogenes or Mycobacterium tuberculosis (Kolls et al., unpublished observations), whe... | [
"44",
"46",
"47"
] | 424 | 43,128 | 0 | false | It is possible that IL-23 and the subsequent IL-17 pathway have evolved to handle extracellular gram-negative bacterial challenges, because IL-17 is not required for host resistance against intracellular organisms such as Listeria monocytogenes or Mycobacterium tuberculosis (Kolls et al., unpublished observations), whe... | [
"44–46"
] | It is possible that IL-23 and the subsequent IL-17 pathway have evolved to handle extracellular gram-negative bacterial challenges, because IL-17 is not required for host resistance against intracellular organisms such as Listeria monocytogenes or Mycobacterium tuberculosis (Kolls et al., unpublished observations), whe... | true | true | true | true | true | 7,468 |
7 | DISCUSSION | 1 | 47 | [
"bib44",
"bib46",
"bib47"
] | 16,157,683 | pmid-9206995|pmid-8245795|pmid-15657292 | Moreover, because IL-23 is critical for autoimmune diseases such as arthritis and multiple sclerosis (47), our data suggest that targeting IL-23 p19 would be less immunosuppressive than IL-12/23 p40. | [
"44",
"46",
"47"
] | 199 | 43,129 | 1 | false | Moreover, because IL-23 is critical for autoimmune diseases such as arthritis and multiple sclerosis, our data suggest that targeting IL-23 p19 would be less immunosuppressive than IL-12/23 p40. | [
"47"
] | Moreover, because IL-23 is critical for autoimmune diseases such as arthritis and multiple sclerosis, our data suggest that targeting IL-23 p19 would be less immunosuppressive than IL-12/23 p40. | true | true | true | true | true | 7,468 |
0 | DISCUSSION | 1 | 10 | [
"B10",
"B11",
"B12"
] | 11,752,981 | pmid-8406422|pmid-1536615|pmid-2642309 | Although granulosa cell tumor is the most common sexcord stromal tumor to occur in the ovary, it is extremely rare in the testis and its origin is poorly understood. | [
"10",
"11",
"12"
] | 165 | 43,130 | 0 | false | Although granulosa cell tumor is the most common sexcord stromal tumor to occur in the ovary, it is extremely rare in the testis and its origin is poorly understood. | [] | Although granulosa cell tumor is the most common sexcord stromal tumor to occur in the ovary, it is extremely rare in the testis and its origin is poorly understood. | true | true | true | true | true | 7,469 |
0 | DISCUSSION | 1 | 10 | [
"B10",
"B11",
"B12"
] | 11,752,981 | pmid-8406422|pmid-1536615|pmid-2642309 | To the best of our knowledge, the literature in English is limited to only 19 cases of adult granulosa cell tumor of the testis (10). | [
"10",
"11",
"12"
] | 133 | 43,131 | 1 | false | To the best of our knowledge, the literature in English is limited to only 19 cases of adult granulosa cell tumor of the testis. | [
"10"
] | To the best of our knowledge, the literature in English is limited to only 19 cases of adult granulosa cell tumor of the testis. | true | true | true | true | true | 7,469 |
0 | DISCUSSION | 1 | 10 | [
"B10",
"B11",
"B12"
] | 11,752,981 | pmid-8406422|pmid-1536615|pmid-2642309 | Moreover, the radiologic findings of this disease entity are not well known. | [
"10",
"11",
"12"
] | 76 | 43,132 | 0 | false | Moreover, the radiologic findings of this disease entity are not well known. | [] | Moreover, the radiologic findings of this disease entity are not well known. | true | true | true | true | true | 7,469 |
0 | DISCUSSION | 1 | 10 | [
"B10",
"B11",
"B12"
] | 11,752,981 | pmid-8406422|pmid-1536615|pmid-2642309 | We are aware of only two previous reports of the US findings of adult-type testicular granulosa cell tumor, and both of these described the tumor as a well-defined hypoechoic testicular mass (11, 12). | [
"10",
"11",
"12"
] | 200 | 43,133 | 0 | false | We are aware of only two previous reports of the US findings of adult-type testicular granulosa cell tumor, and both of these described the tumor as a well-defined hypoechoic testicular mass. | [
"11, 12"
] | We are aware of only two previous reports of the US findings of adult-type testicular granulosa cell tumor, and both of these described the tumor as a well-defined hypoechoic testicular mass. | true | true | true | true | true | 7,469 |
1 | DISCUSSION | 1 | 13 | [
"B13",
"B14",
"B9"
] | 11,752,981 | pmid-9591732|pmid-1847943|pmid-7020914 | In our case, the tumor appeared to arise from the scrotal tunics, an unusual location for a sex-cord stromal tumor. | [
"13",
"14",
"9"
] | 115 | 43,134 | 0 | false | In our case, the tumor appeared to arise from the scrotal tunics, an unusual location for a sex-cord stromal tumor. | [] | In our case, the tumor appeared to arise from the scrotal tunics, an unusual location for a sex-cord stromal tumor. | true | true | true | true | true | 7,470 |
1 | DISCUSSION | 1 | 13 | [
"B13",
"B14",
"B9"
] | 11,752,981 | pmid-9591732|pmid-1847943|pmid-7020914 | It was, however, because of the presence of typical large indented nuclei with longitudinal nuclear grooves and Call-Exner bodies, as well as positive immunoreactivity for inhibin, keratin and vimentin, that granulosa cell tumor was diagnosed (13). | [
"13",
"14",
"9"
] | 248 | 43,135 | 1 | false | It was, however, because of the presence of typical large indented nuclei with longitudinal nuclear grooves and Call-Exner bodies, as well as positive immunoreactivity for inhibin, keratin and vimentin, that granulosa cell tumor was diagnosed. | [
"13"
] | It was, however, because of the presence of typical large indented nuclei with longitudinal nuclear grooves and Call-Exner bodies, as well as positive immunoreactivity for inhibin, keratin and vimentin, that granulosa cell tumor was diagnosed. | true | true | true | true | true | 7,470 |
1 | DISCUSSION | 1 | 14 | [
"B13",
"B14",
"B9"
] | 11,752,981 | pmid-9591732|pmid-1847943|pmid-7020914 | Fourteen percent of all paratesticular tumors arise from the scrotal tunics and among these, benign fibroma, representing a fibrous reaction to chronic periorchitis, is the most common lesion (14). | [
"13",
"14",
"9"
] | 197 | 43,136 | 1 | false | Fourteen percent of all paratesticular tumors arise from the scrotal tunics and among these, benign fibroma, representing a fibrous reaction to chronic periorchitis, is the most common lesion. | [
"14"
] | Fourteen percent of all paratesticular tumors arise from the scrotal tunics and among these, benign fibroma, representing a fibrous reaction to chronic periorchitis, is the most common lesion. | true | true | true | true | true | 7,470 |
1 | DISCUSSION | 1 | 9 | [
"B13",
"B14",
"B9"
] | 11,752,981 | pmid-9591732|pmid-1847943|pmid-7020914 | Although granulosa cell tumor arising from the scrotal tunics has not been previously reported, extratesticular sex-cord stromal tumor in the pelvis has been described (9). | [
"13",
"14",
"9"
] | 172 | 43,137 | 1 | false | Although granulosa cell tumor arising from the scrotal tunics has not been previously reported, extratesticular sex-cord stromal tumor in the pelvis has been described. | [
"9"
] | Although granulosa cell tumor arising from the scrotal tunics has not been previously reported, extratesticular sex-cord stromal tumor in the pelvis has been described. | true | true | true | true | true | 7,470 |
1 | DISCUSSION | 1 | 13 | [
"B13",
"B14",
"B9"
] | 11,752,981 | pmid-9591732|pmid-1847943|pmid-7020914 | The suggested explanation is that the tumor originated in a residual part of the primitive gonad or a third undescended testis which was completely destroyed by the process, and we believe that in our case the same explanation is possible. | [
"13",
"14",
"9"
] | 239 | 43,138 | 0 | false | The suggested explanation is that the tumor originated in a residual part of the primitive gonad or a third undescended testis which was completely destroyed by the process, and we believe that in our case the same explanation is possible. | [] | The suggested explanation is that the tumor originated in a residual part of the primitive gonad or a third undescended testis which was completely destroyed by the process, and we believe that in our case the same explanation is possible. | true | true | true | true | true | 7,470 |
2 | DISCUSSION | 0 | null | null | 11,752,981 | null | Pathologic examination indicated that this tumor had originated from and was confined to the scrotal tunics. | null | 108 | 43,139 | 0 | false | null | null | Pathologic examination indicated that this tumor had originated from and was confined to the scrotal tunics. | true | true | true | true | true | 7,471 |
2 | DISCUSSION | 0 | null | null | 11,752,981 | null | The testis and epididymis were normal and easily separated from the tumor. | null | 74 | 43,140 | 0 | false | null | null | The testis and epididymis were normal and easily separated from the tumor. | true | true | true | true | true | 7,471 |
2 | DISCUSSION | 0 | null | null | 11,752,981 | null | Nevertheless, because the largest nodule was deeply invaginated into the testis, displacing the epididymis, which was compressed and not visualized, the location of this tumor - according to the findings of US and MR imaging - was intratesticular and epididymal. | null | 262 | 43,141 | 0 | false | null | null | Nevertheless, because the largest nodule was deeply invaginated into the testis, displacing the epididymis, which was compressed and not visualized, the location of this tumor - according to the findings of US and MR imaging - was intratesticular and epididymal. | true | true | true | true | true | 7,471 |
2 | DISCUSSION | 0 | null | null | 11,752,981 | null | It was because the main lesion was in the testis and epididymis, and multiple small nodules were attached to the inner scrotal wall, that malignancy was suspected. | null | 163 | 43,142 | 0 | false | null | null | It was because the main lesion was in the testis and epididymis, and multiple small nodules were attached to the inner scrotal wall, that malignancy was suspected. | true | true | true | true | true | 7,471 |
2 | DISCUSSION | 0 | null | null | 11,752,981 | null | On the other hand, because of extensive hydrocele, the lesion also mimicked an inflammatory condition such as tuberculous epididymo-orchitis. | null | 141 | 43,143 | 0 | false | null | null | On the other hand, because of extensive hydrocele, the lesion also mimicked an inflammatory condition such as tuberculous epididymo-orchitis. | true | true | true | true | true | 7,471 |
2 | DISCUSSION | 0 | null | null | 11,752,981 | null | The only clue to the origin of the mass was the low-signal-intensity rim between the lesion and the testis revealed by T2-weighted imaging. | null | 139 | 43,144 | 0 | false | null | null | The only clue to the origin of the mass was the low-signal-intensity rim between the lesion and the testis revealed by T2-weighted imaging. | true | true | true | true | true | 7,471 |
3 | DISCUSSION | 0 | null | null | 11,752,981 | null | To our knowledge, this is the first reported case of paratesticular granulosa cell tumor, and it would therefore be premature to state that the US and MR features of our case are specific to granulosa cell tumor of the scrotal tunics. | null | 234 | 43,145 | 0 | false | null | null | To our knowledge, this is the first reported case of paratesticular granulosa cell tumor, and it would therefore be premature to state that the US and MR features of our case are specific to granulosa cell tumor of the scrotal tunics. | true | true | true | true | true | 7,472 |
3 | DISCUSSION | 0 | null | null | 11,752,981 | null | Although the formulation of a treatment plan might not require specific diagnosis, we suggest that the presence of a mass seen as an intratesticular lesion associated with multiple enhancing nodules attached to scrotal tunics indicates the possibility of a paratesticular tumor, and that granulosa cell tumor should be i... | null | 358 | 43,146 | 0 | false | null | null | Although the formulation of a treatment plan might not require specific diagnosis, we suggest that the presence of a mass seen as an intratesticular lesion associated with multiple enhancing nodules attached to scrotal tunics indicates the possibility of a paratesticular tumor, and that granulosa cell tumor should be i... | true | true | true | true | true | 7,472 |
3 | DISCUSSION | 0 | null | null | 11,752,981 | null | We believe that MR imaging findings of a peripheral low-signal-intensity rim on a T2-weighted image might help determine the origin of the mass. | null | 144 | 43,147 | 0 | false | null | null | We believe that MR imaging findings of a peripheral low-signal-intensity rim on a T2-weighted image might help determine the origin of the mass. | true | true | true | true | true | 7,472 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | The production of lipid mediators, the eicosanoids (i.e. | [
"1–3",
"4",
"5",
"6",
"7"
] | 56 | 43,148 | 0 | false | The production of lipid mediators, the eicosanoids (i.e. | [] | The production of lipid mediators, the eicosanoids (i.e. | true | true | true | true | true | 7,473 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | prostaglandins and leukotrienes) are derived from metabolism of arachidonic acid, which has been implicated in the regulation of cell growth, inflammation, thrombosis and tumor progression (1–3). | [
"1–3",
"4",
"5",
"6",
"7"
] | 195 | 43,149 | 1 | false | prostaglandins and leukotrienes) are derived from metabolism of arachidonic acid, which has been implicated in the regulation of cell growth, inflammation, thrombosis and tumor progression. | [
"1–3"
] | prostaglandins and leukotrienes) are derived from metabolism of arachidonic acid, which has been implicated in the regulation of cell growth, inflammation, thrombosis and tumor progression. | false | true | true | true | false | 7,473 |
0 | INTRODUCTION | 1 | 4 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | There is much evidence indicating that eicosanoids, particularly prostaglandins, are involved in the etiologies of cancer (4). | [
"1–3",
"4",
"5",
"6",
"7"
] | 126 | 43,150 | 1 | false | There is much evidence indicating that eicosanoids, particularly prostaglandins, are involved in the etiologies of cancer. | [
"4"
] | There is much evidence indicating that eicosanoids, particularly prostaglandins, are involved in the etiologies of cancer. | true | true | true | true | true | 7,473 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | Increased levels of eicosanoids occur in a number of different types of human cancer, including colon, pancreatic, breast and lung. | [
"1–3",
"4",
"5",
"6",
"7"
] | 131 | 43,151 | 0 | false | Increased levels of eicosanoids occur in a number of different types of human cancer, including colon, pancreatic, breast and lung. | [] | Increased levels of eicosanoids occur in a number of different types of human cancer, including colon, pancreatic, breast and lung. | true | true | true | true | true | 7,473 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | In the case of lung cancer, increased prostaglandin biosynthesis has been found to occur mainly in non-small cell lung cancer (NSCLC), which comprises 80% of lung cancers rather than small cell lung cancer (SCLC) (5,6). | [
"1–3",
"4",
"5",
"6",
"7"
] | 219 | 43,152 | 0 | false | In the case of lung cancer, increased prostaglandin biosynthesis has been found to occur mainly in non-small cell lung cancer (NSCLC), which comprises 80% of lung cancers rather than small cell lung cancer (SCLC). | [
"5,6"
] | In the case of lung cancer, increased prostaglandin biosynthesis has been found to occur mainly in non-small cell lung cancer (NSCLC), which comprises 80% of lung cancers rather than small cell lung cancer (SCLC). | true | true | true | true | true | 7,473 |
0 | INTRODUCTION | 1 | 7 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | In addition, the increase of cPLA2 is correlated with the eicosanoid synthesis that participates in NSCLC transformation (7). | [
"1–3",
"4",
"5",
"6",
"7"
] | 125 | 43,153 | 1 | false | In addition, the increase of cPLA2 is correlated with the eicosanoid synthesis that participates in NSCLC transformation. | [
"7"
] | In addition, the increase of cPLA2 is correlated with the eicosanoid synthesis that participates in NSCLC transformation. | true | true | true | true | true | 7,473 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14 B15 B16",
"B17 B18 B19 B20 B21",
"B18",
"B22",
"B23",
"B24",
"B25"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Cytosolic phospholipase A2 (cPLA2) is the major intracellular form of PLA2, which preferentially hydrolyzes membrane phospholipids at the sn-2 position to release arachidonic acid (8). | [
"8",
"9",
"10",
"11",
"12",
"13",
"14–16",
"17–21",
"18",
"22",
"23",
"24",
"25"
] | 184 | 43,154 | 1 | false | Cytosolic phospholipase A2 (cPLA2) is the major intracellular form of PLA2, which preferentially hydrolyzes membrane phospholipids at the sn-2 position to release arachidonic acid. | [
"8"
] | Cytosolic phospholipase A2 (cPLA2) is the major intracellular form of PLA2, which preferentially hydrolyzes membrane phospholipids at the sn-2 position to release arachidonic acid. | true | true | true | true | true | 7,474 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14 B15 B16",
"B17 B18 B19 B20 B21",
"B18",
"B22",
"B23",
"B24",
"B25"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | cPLA2 activity is regulated by intracellular Ca2+ and phosphorylation. | [
"8",
"9",
"10",
"11",
"12",
"13",
"14–16",
"17–21",
"18",
"22",
"23",
"24",
"25"
] | 70 | 43,155 | 0 | false | cPLA2 activity is regulated by intracellular Ca2+ and phosphorylation. | [] | cPLA2 activity is regulated by intracellular Ca2+ and phosphorylation. | false | true | true | true | false | 7,474 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14 B15 B16",
"B17 B18 B19 B20 B21",
"B18",
"B22",
"B23",
"B24",
"B25"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Increase in Ca2+ results in translocation of cPLA2 to the nuclear envelope and activation (9,10). | [
"8",
"9",
"10",
"11",
"12",
"13",
"14–16",
"17–21",
"18",
"22",
"23",
"24",
"25"
] | 97 | 43,156 | 0 | false | Increase in Ca2+ results in translocation of cPLA2 to the nuclear envelope and activation. | [
"9,10"
] | Increase in Ca2+ results in translocation of cPLA2 to the nuclear envelope and activation. | true | true | true | true | true | 7,474 |
1 | INTRODUCTION | 1 | 13 | [
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14 B15 B16",
"B17 B18 B19 B20 B21",
"B18",
"B22",
"B23",
"B24",
"B25"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | But it has been shown that phorbol 12-myristate 13-acetate (PMA) provides cPLA2-activating signals without inducing Ca2+ influx (11,12) and by a Rac-p38 kinase-dependent pathway (13). | [
"8",
"9",
"10",
"11",
"12",
"13",
"14–16",
"17–21",
"18",
"22",
"23",
"24",
"25"
] | 183 | 43,157 | 1 | false | But it has been shown that phorbol 12-myristate 13-acetate (PMA) provides cPLA2-activating signals without inducing Ca2+ influx and by a Rac-p38 kinase-dependent pathway. | [
"11,12",
"13"
] | But it has been shown that phorbol 12-myristate 13-acetate (PMA) provides cPLA2-activating signals without inducing Ca2+ influx and by a Rac-p38 kinase-dependent pathway. | true | true | true | true | true | 7,474 |
1 | INTRODUCTION | 1 | 14–16 | [
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14 B15 B16",
"B17 B18 B19 B20 B21",
"B18",
"B22",
"B23",
"B24",
"B25"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | The maximal activation of cPLA2 requires sustained phosphorylation of Ser505, Ser727 and Ser515 by mitogen-activated protein kinases (MAPKs), MAPK-activated protein kinases and by calcium/calmodulin-dependent protein kinase II, respectively (14–16). | [
"8",
"9",
"10",
"11",
"12",
"13",
"14–16",
"17–21",
"18",
"22",
"23",
"24",
"25"
] | 249 | 43,158 | 1 | false | The maximal activation of cPLA2 requires sustained phosphorylation of Ser505, Ser727 and Ser515 by mitogen-activated protein kinases (MAPKs), MAPK-activated protein kinases and by calcium/calmodulin-dependent protein kinase II, respectively. | [
"14–16"
] | The maximal activation of cPLA2 requires sustained phosphorylation of Ser505, Ser727 and Ser515 by mitogen-activated protein kinases (MAPKs), MAPK-activated protein kinases and by calcium/calmodulin-dependent protein kinase II, respectively. | true | true | true | true | true | 7,474 |
1 | INTRODUCTION | 1 | 17–21 | [
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14 B15 B16",
"B17 B18 B19 B20 B21",
"B18",
"B22",
"B23",
"B24",
"B25"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | In addition to acute regulation, expression of cPLA2 through changes in gene transcription is mediated by a number of agents including cytokines, thrombin and growth factors (17–21). | [
"8",
"9",
"10",
"11",
"12",
"13",
"14–16",
"17–21",
"18",
"22",
"23",
"24",
"25"
] | 182 | 43,159 | 1 | false | In addition to acute regulation, expression of cPLA2 through changes in gene transcription is mediated by a number of agents including cytokines, thrombin and growth factors. | [
"17–21"
] | In addition to acute regulation, expression of cPLA2 through changes in gene transcription is mediated by a number of agents including cytokines, thrombin and growth factors. | true | true | true | true | true | 7,474 |
1 | INTRODUCTION | 1 | 18 | [
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14 B15 B16",
"B17 B18 B19 B20 B21",
"B18",
"B22",
"B23",
"B24",
"B25"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | The promoter for cPLA2 has been isolated from both human (18) and rat (22). | [
"8",
"9",
"10",
"11",
"12",
"13",
"14–16",
"17–21",
"18",
"22",
"23",
"24",
"25"
] | 75 | 43,160 | 1 | false | The promoter for cPLA2 has been isolated from both human and rat. | [
"18",
"22"
] | The promoter for cPLA2 has been isolated from both human and rat. | true | true | true | true | true | 7,474 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14 B15 B16",
"B17 B18 B19 B20 B21",
"B18",
"B22",
"B23",
"B24",
"B25"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | A number of putative binding sites for possible regulatory elements have been identified within the promoter, including AP-1 sites, nuclear factor κB sites and glucocorticoid regulatory elements. | [
"8",
"9",
"10",
"11",
"12",
"13",
"14–16",
"17–21",
"18",
"22",
"23",
"24",
"25"
] | 195 | 43,161 | 0 | false | A number of putative binding sites for possible regulatory elements have been identified within the promoter, including AP-1 sites, nuclear factor κB sites and glucocorticoid regulatory elements. | [] | A number of putative binding sites for possible regulatory elements have been identified within the promoter, including AP-1 sites, nuclear factor κB sites and glucocorticoid regulatory elements. | true | true | true | true | true | 7,474 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14 B15 B16",
"B17 B18 B19 B20 B21",
"B18",
"B22",
"B23",
"B24",
"B25"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Truncation of a 2.4 kb region of the promoter fragment down to the last 58 bp of the 5′-untranslated region has been identified in three regulatory regions and indicates that the transcription factor Sp1 can bind to two of these regions (23,24). | [
"8",
"9",
"10",
"11",
"12",
"13",
"14–16",
"17–21",
"18",
"22",
"23",
"24",
"25"
] | 245 | 43,162 | 0 | false | Truncation of a 2.4 kb region of the promoter fragment down to the last 58 bp of the 5′-untranslated region has been identified in three regulatory regions and indicates that the transcription factor Sp1 can bind to two of these regions. | [
"23,24"
] | Truncation of a 2.4 kb region of the promoter fragment down to the last 58 bp of the 5′-untranslated region has been identified in three regulatory regions and indicates that the transcription factor Sp1 can bind to two of these regions. | true | true | true | true | true | 7,474 |
1 | INTRODUCTION | 1 | 25 | [
"B8",
"B9",
"B10",
"B11",
"B12",
"B13",
"B14 B15 B16",
"B17 B18 B19 B20 B21",
"B18",
"B22",
"B23",
"B24",
"B25"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | In the regulation of cPLA2 promoter, LKLF (lung Krüppel-like factor) as a transcriptional activator also binds to the cPLA2 promoter and may interact with the Sp1 family (25). | [
"8",
"9",
"10",
"11",
"12",
"13",
"14–16",
"17–21",
"18",
"22",
"23",
"24",
"25"
] | 175 | 43,163 | 1 | false | In the regulation of cPLA2 promoter, LKLF (lung Krüppel-like factor) as a transcriptional activator also binds to the cPLA2 promoter and may interact with the Sp1 family. | [
"25"
] | In the regulation of cPLA2 promoter, LKLF (lung Krüppel-like factor) as a transcriptional activator also binds to the cPLA2 promoter and may interact with the Sp1 family. | true | true | true | true | true | 7,474 |
2 | INTRODUCTION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B30",
"B31"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Although Sp1 is required for the transcriptional activation of cPLA2 gene, only a limited number of studies have addressed the mechanisms by which cPLA2 gene expression is controlled. | [
"26–29",
"30",
"31"
] | 183 | 43,164 | 0 | false | Although Sp1 is required for the transcriptional activation of cPLA2 gene, only a limited number of studies have addressed the mechanisms by which cPLA2 gene expression is controlled. | [] | Although Sp1 is required for the transcriptional activation of cPLA2 gene, only a limited number of studies have addressed the mechanisms by which cPLA2 gene expression is controlled. | true | true | true | true | true | 7,475 |
2 | INTRODUCTION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B30",
"B31"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | In addition to enzymatic activation, in this study, we also clarified that PMA could activate the transcription via the Sp1-binding sites of cPLA2α promoter in NSCLC A549 cells. | [
"26–29",
"30",
"31"
] | 177 | 43,165 | 0 | false | In addition to enzymatic activation, in this study, we also clarified that PMA could activate the transcription via the Sp1-binding sites of cPLA2α promoter in NSCLC A549 cells. | [] | In addition to enzymatic activation, in this study, we also clarified that PMA could activate the transcription via the Sp1-binding sites of cPLA2α promoter in NSCLC A549 cells. | true | true | true | true | true | 7,475 |
2 | INTRODUCTION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B30",
"B31"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | We demonstrated that transcription factors c-Jun and Sp1 form a complex to regulate PMA-induced gene expression of cPLA2α as the manner as the c-Jun/Sp1-regulated genes including 12(S)-lipoxygenase, keratin 16, p21WAF1/CIP1 and neuronal nicotinic acetylcholine receptor β4 (26–29). | [
"26–29",
"30",
"31"
] | 281 | 43,166 | 1 | false | We demonstrated that transcription factors c-Jun and Sp1 form a complex to regulate PMA-induced gene expression of cPLA2α as the manner as the c-Jun/Sp1-regulated genes including 12(S)-lipoxygenase, keratin 16, p21WAF1/CIP1 and neuronal nicotinic acetylcholine receptor β4. | [
"26–29"
] | We demonstrated that transcription factors c-Jun and Sp1 form a complex to regulate PMA-induced gene expression of cPLA2α as the manner as the c-Jun/Sp1-regulated genes including 12(S)-lipoxygenase, keratin 16, p21WAF1/CIP1 and neuronal nicotinic acetylcholine receptor β4. | true | true | true | true | true | 7,475 |
2 | INTRODUCTION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B30",
"B31"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | We further performed pull-down and protein–DNA interaction assays to show that nucleolin bound to DNA and activated transcription of cPLA2α in PMA-treated cells. | [
"26–29",
"30",
"31"
] | 161 | 43,167 | 0 | false | We further performed pull-down and protein–DNA interaction assays to show that nucleolin bound to DNA and activated transcription of cPLA2α in PMA-treated cells. | [] | We further performed pull-down and protein–DNA interaction assays to show that nucleolin bound to DNA and activated transcription of cPLA2α in PMA-treated cells. | true | true | true | true | true | 7,475 |
2 | INTRODUCTION | 1 | 30 | [
"B26 B27 B28 B29",
"B30",
"B31"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Nucleolin is reported to be a ubiquitously expressed multifunctional protein involved in ribosomal biogenesis and the regulation of nucleolar translocation of ribosomal proteins (30). | [
"26–29",
"30",
"31"
] | 183 | 43,168 | 1 | false | Nucleolin is reported to be a ubiquitously expressed multifunctional protein involved in ribosomal biogenesis and the regulation of nucleolar translocation of ribosomal proteins. | [
"30"
] | Nucleolin is reported to be a ubiquitously expressed multifunctional protein involved in ribosomal biogenesis and the regulation of nucleolar translocation of ribosomal proteins. | true | true | true | true | true | 7,475 |
2 | INTRODUCTION | 1 | 31 | [
"B26 B27 B28 B29",
"B30",
"B31"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Functional role of nucleolin in the activation and repression of gene transcription as well as in the regulation of RNA metabolism has already been reported (31). | [
"26–29",
"30",
"31"
] | 162 | 43,169 | 1 | false | Functional role of nucleolin in the activation and repression of gene transcription as well as in the regulation of RNA metabolism has already been reported. | [
"31"
] | Functional role of nucleolin in the activation and repression of gene transcription as well as in the regulation of RNA metabolism has already been reported. | true | true | true | true | true | 7,475 |
2 | INTRODUCTION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B30",
"B31"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Our results revealed a new function for nucleolin as a c-Jun/Sp1-interacting partner and transcription activator in PMA-induced gene expression of cPLA2α. | [
"26–29",
"30",
"31"
] | 154 | 43,170 | 0 | false | Our results revealed a new function for nucleolin as a c-Jun/Sp1-interacting partner and transcription activator in PMA-induced gene expression of cPLA2α. | [] | Our results revealed a new function for nucleolin as a c-Jun/Sp1-interacting partner and transcription activator in PMA-induced gene expression of cPLA2α. | true | true | true | true | true | 7,475 |
0 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B41",
"B42",
"B43"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | The expression of cPLA2 can be regulated in NSCLC (7) and is critical for transformed growth of NSCLC. | [
"7",
"7",
"41",
"42",
"43"
] | 102 | 43,171 | 1 | false | The expression of cPLA2 can be regulated in NSCLC and is critical for transformed growth of NSCLC. | [
"7"
] | The expression of cPLA2 can be regulated in NSCLC and is critical for transformed growth of NSCLC. | true | true | true | true | true | 7,476 |
0 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B41",
"B42",
"B43"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | When these cells are treated with a specific inhibitor of the enzyme, or blocking downstream production of prostaglandins with cyclooxygenase inhibitors, resulting in inhibition of anchorage-independent growth of these cells (7). | [
"7",
"7",
"41",
"42",
"43"
] | 229 | 43,172 | 1 | false | When these cells are treated with a specific inhibitor of the enzyme, or blocking downstream production of prostaglandins with cyclooxygenase inhibitors, resulting in inhibition of anchorage-independent growth of these cells. | [
"7"
] | When these cells are treated with a specific inhibitor of the enzyme, or blocking downstream production of prostaglandins with cyclooxygenase inhibitors, resulting in inhibition of anchorage-independent growth of these cells. | true | true | true | true | true | 7,476 |
0 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B41",
"B42",
"B43"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | These results suggest that induction of cPLA2 is critical for tumorigenesis. | [
"7",
"7",
"41",
"42",
"43"
] | 76 | 43,173 | 0 | false | These results suggest that induction of cPLA2 is critical for tumorigenesis. | [] | These results suggest that induction of cPLA2 is critical for tumorigenesis. | true | true | true | true | true | 7,476 |
0 | DISCUSSION | 1 | 41 | [
"B7",
"B7",
"B41",
"B42",
"B43"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | Consistent with this finding, lung tumorigenesis is inhibited in mice that are deficient in cPLA2 (41). | [
"7",
"7",
"41",
"42",
"43"
] | 103 | 43,174 | 1 | false | Consistent with this finding, lung tumorigenesis is inhibited in mice that are deficient in cPLA2. | [
"41"
] | Consistent with this finding, lung tumorigenesis is inhibited in mice that are deficient in cPLA2. | true | true | true | true | true | 7,476 |
0 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B41",
"B42",
"B43"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | In this study, we first found that PMA induced gene expression of cPLA2α in NSCLC. | [
"7",
"7",
"41",
"42",
"43"
] | 82 | 43,175 | 0 | false | In this study, we first found that PMA induced gene expression of cPLA2α in NSCLC. | [] | In this study, we first found that PMA induced gene expression of cPLA2α in NSCLC. | true | true | true | true | true | 7,476 |
0 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B41",
"B42",
"B43"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | It has been known that PMA-activated PKC signal transduction pathway is thought to be involved in the oncogene action in NSCLC and enzymatic activation of cPLA2. | [
"7",
"7",
"41",
"42",
"43"
] | 161 | 43,176 | 0 | false | It has been known that PMA-activated PKC signal transduction pathway is thought to be involved in the oncogene action in NSCLC and enzymatic activation of cPLA2. | [] | It has been known that PMA-activated PKC signal transduction pathway is thought to be involved in the oncogene action in NSCLC and enzymatic activation of cPLA2. | true | true | true | true | true | 7,476 |
0 | DISCUSSION | 1 | 42 | [
"B7",
"B7",
"B41",
"B42",
"B43"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | Activation of PKC with PMA impairs progression of lung adenocarcinoma cells from early G1 phase into S phase (42). | [
"7",
"7",
"41",
"42",
"43"
] | 114 | 43,177 | 1 | false | Activation of PKC with PMA impairs progression of lung adenocarcinoma cells from early G1 phase into S phase. | [
"42"
] | Activation of PKC with PMA impairs progression of lung adenocarcinoma cells from early G1 phase into S phase. | true | true | true | true | true | 7,476 |
0 | DISCUSSION | 1 | 43 | [
"B7",
"B7",
"B41",
"B42",
"B43"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | The broad-range PKC inhibitor staurosporine analog, PKC 412, induces apoptosis in SCLC cells and sensitizes NSCLC cells to apoptosis induced by DNA-damaging agents (43). | [
"7",
"7",
"41",
"42",
"43"
] | 169 | 43,178 | 1 | false | The broad-range PKC inhibitor staurosporine analog, PKC 412, induces apoptosis in SCLC cells and sensitizes NSCLC cells to apoptosis induced by DNA-damaging agents. | [
"43"
] | The broad-range PKC inhibitor staurosporine analog, PKC 412, induces apoptosis in SCLC cells and sensitizes NSCLC cells to apoptosis induced by DNA-damaging agents. | true | true | true | true | true | 7,476 |
0 | DISCUSSION | 1 | 7 | [
"B7",
"B7",
"B41",
"B42",
"B43"
] | 18,025,046 | pmid-12088280|pmid-15950989|pmid-15896353|pmid-11901304|pmid-3409218|pmid-3130187|pmid-9169405|pmid-9169405|pmid-9169405|pmid-15033900|pmid-16055435|pmid-15777800 | Taking these results together, we concluded that PMA-induced expression of cPLA2α might be related to either a cause or a consequence of PMA-regulated tumorigenesis of NSCLC. | [
"7",
"7",
"41",
"42",
"43"
] | 174 | 43,179 | 0 | false | Taking these results together, we concluded that PMA-induced expression of cPLA2α might be related to either a cause or a consequence of PMA-regulated tumorigenesis of NSCLC. | [] | Taking these results together, we concluded that PMA-induced expression of cPLA2α might be related to either a cause or a consequence of PMA-regulated tumorigenesis of NSCLC. | true | true | true | true | true | 7,476 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | In the regulation of gene expression, previous studies have reported that c-Jun/Sp1 complex is critical for various different gene expressions, e.g. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 148 | 43,180 | 0 | false | In the regulation of gene expression, previous studies have reported that c-Jun/Sp1 complex is critical for various different gene expressions, e.g. | [] | In the regulation of gene expression, previous studies have reported that c-Jun/Sp1 complex is critical for various different gene expressions, e.g. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | 12(S)-lipoxygenase, keratin 16, p21WAF1/CIP1 and neuronal nicotinic acetylcholine receptor β4 (26–29). | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 102 | 43,181 | 1 | false | 12(S)-lipoxygenase, keratin 16, p21WAF1/CIP1 and neuronal nicotinic acetylcholine receptor β4. | [
"26–29"
] | 12(S)-lipoxygenase, keratin 16, p21WAF1/CIP1 and neuronal nicotinic acetylcholine receptor β4. | false | false | true | true | false | 7,477 |
1 | DISCUSSION | 1 | 23 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Although overexpression of c-Jun and Sp1 produces a synergistic increase in the rat cPLA2 promoter activity, no evidence shows that the formation of c-Jun/Sp1 complex and the complex binding to the rat cPLA2 promoter are observed (23). | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 235 | 43,182 | 1 | false | Although overexpression of c-Jun and Sp1 produces a synergistic increase in the rat cPLA2 promoter activity, no evidence shows that the formation of c-Jun/Sp1 complex and the complex binding to the rat cPLA2 promoter are observed. | [
"23"
] | Although overexpression of c-Jun and Sp1 produces a synergistic increase in the rat cPLA2 promoter activity, no evidence shows that the formation of c-Jun/Sp1 complex and the complex binding to the rat cPLA2 promoter are observed. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | However, we first clarified that PMA induced c-Jun/Sp1 interaction and the complex bound to Sp1-binding sites of human cPLA2α promoter, resulting in the induction of transcriptional activation. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 193 | 43,183 | 0 | false | However, we first clarified that PMA induced c-Jun/Sp1 interaction and the complex bound to Sp1-binding sites of human cPLA2α promoter, resulting in the induction of transcriptional activation. | [] | However, we first clarified that PMA induced c-Jun/Sp1 interaction and the complex bound to Sp1-binding sites of human cPLA2α promoter, resulting in the induction of transcriptional activation. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | In addition, we found that nucleolin was also a coactivator interacting with c-Jun to regulate PMA-induced transcription of cPLA2α gene. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 136 | 43,184 | 0 | false | In addition, we found that nucleolin was also a coactivator interacting with c-Jun to regulate PMA-induced transcription of cPLA2α gene. | [] | In addition, we found that nucleolin was also a coactivator interacting with c-Jun to regulate PMA-induced transcription of cPLA2α gene. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 30 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Nucleolin is a ubiquitous, nonhistone nucleolar phosphoprotein of exponentially growing eukaryotic cells, which is directly involved in the regulation of ribosome biogenesis, the processing of ribosomal RNA, mRNA stability, transcriptional regulation and cell proliferation, and it is also a downstream target of several... | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 355 | 43,185 | 1 | false | Nucleolin is a ubiquitous, nonhistone nucleolar phosphoprotein of exponentially growing eukaryotic cells, which is directly involved in the regulation of ribosome biogenesis, the processing of ribosomal RNA, mRNA stability, transcriptional regulation and cell proliferation, and it is also a downstream target of several... | [
"30"
] | Nucleolin is a ubiquitous, nonhistone nucleolar phosphoprotein of exponentially growing eukaryotic cells, which is directly involved in the regulation of ribosome biogenesis, the processing of ribosomal RNA, mRNA stability, transcriptional regulation and cell proliferation, and it is also a downstream target of several... | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Matching our results, the functional role of nucleolin involved in the transcriptional activation of gene expression has been found. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 132 | 43,186 | 0 | false | Matching our results, the functional role of nucleolin involved in the transcriptional activation of gene expression has been found. | [] | Matching our results, the functional role of nucleolin involved in the transcriptional activation of gene expression has been found. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 44 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Nucleolin binds acetylated interferon regulatory factor-2 (IRF-2) to enhance H4 promoter activity (44) and plays as a key activator of HPV18 oncogene transcription in cervical cancer (45). | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 188 | 43,187 | 1 | false | Nucleolin binds acetylated interferon regulatory factor-2 (IRF-2) to enhance H4 promoter activity and plays as a key activator of HPV18 oncogene transcription in cervical cancer. | [
"44",
"45"
] | Nucleolin binds acetylated interferon regulatory factor-2 (IRF-2) to enhance H4 promoter activity and plays as a key activator of HPV18 oncogene transcription in cervical cancer. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Nucleolin also binds transcription factors Myb and tumor suppressor Rb to regulate Myb transcriptional activity and tumor development (46,47). | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 142 | 43,188 | 0 | false | Nucleolin also binds transcription factors Myb and tumor suppressor Rb to regulate Myb transcriptional activity and tumor development. | [
"46,47"
] | Nucleolin also binds transcription factors Myb and tumor suppressor Rb to regulate Myb transcriptional activity and tumor development. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | These findings suggest that nucleolin may act as a transcriptional regulator via interacting with activators. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 109 | 43,189 | 0 | false | These findings suggest that nucleolin may act as a transcriptional regulator via interacting with activators. | [] | These findings suggest that nucleolin may act as a transcriptional regulator via interacting with activators. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Indeed, in the experiments of immunoprecipitation and DAPA, we found that nucleolin bound and bridged c-Jun to Sp1-binding sites of cPLA2α promoter (Figures 4C and 7B). | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 168 | 43,190 | 0 | false | Indeed, in the experiments of immunoprecipitation and DAPA, we found that nucleolin bound and bridged c-Jun to Sp1-binding sites of cPLA2α promoter (Figures 4C and 7B). | [] | Indeed, in the experiments of immunoprecipitation and DAPA, we found that nucleolin bound and bridged c-Jun to Sp1-binding sites of cPLA2α promoter (Figures 4C and 7B). | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | These results suggested the possibility that nucleolin participated in the regulation of c-Jun/Sp1-regulated genes, e.g. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 120 | 43,191 | 0 | false | These results suggested the possibility that nucleolin participated in the regulation of c-Jun/Sp1-regulated genes, e.g. | [] | These results suggested the possibility that nucleolin participated in the regulation of c-Jun/Sp1-regulated genes, e.g. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 48 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | 12(S)-lipoxygenase (Figure 7D) and p21WAF1/CIP1 to regulate cell growth (48). | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 77 | 43,192 | 1 | false | 12(S)-lipoxygenase (Figure 7D) and p21WAF1/CIP1 to regulate cell growth. | [
"48"
] | 12(S)-lipoxygenase (Figure 7D) and p21WAF1/CIP1 to regulate cell growth. | false | false | true | true | false | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | From our study, we can conclude that for PMA-induced cPLA2α gene expression, and nucleolin acts as a coactivator via cooperation of c-Jun transcriptional factor. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 161 | 43,193 | 0 | false | From our study, we can conclude that for PMA-induced cPLA2α gene expression, and nucleolin acts as a coactivator via cooperation of c-Jun transcriptional factor. | [] | From our study, we can conclude that for PMA-induced cPLA2α gene expression, and nucleolin acts as a coactivator via cooperation of c-Jun transcriptional factor. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | However, the nucleolin/c-Jun complex had no effect on AP1-regulated promoter activation (Figures 6C and 8B). | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 108 | 43,194 | 0 | false | However, the nucleolin/c-Jun complex had no effect on AP1-regulated promoter activation (Figures 6C and 8B). | [] | However, the nucleolin/c-Jun complex had no effect on AP1-regulated promoter activation. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | The different binding affinity between nucleolin/c-Jun to Sp1-binding site and to AP1-binding site might be caused by the stereo-recognition of complex to the Sp1 binding but not AP1-binding sequences. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 201 | 43,195 | 0 | false | The different binding affinity between nucleolin/c-Jun to Sp1-binding site and to AP1-binding site might be caused by the stereo-recognition of complex to the Sp1 binding but not AP1-binding sequences. | [] | The different binding affinity between nucleolin/c-Jun to Sp1-binding site and to AP1-binding site might be caused by the stereo-recognition of complex to the Sp1 binding but not AP1-binding sequences. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Consistent with the role of nucleolin in the regulation of mRNA stability, we found that nucleolin also contributed to the stabilization of cPLA2α mRNA. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 152 | 43,196 | 0 | false | Consistent with the role of nucleolin in the regulation of mRNA stability, we found that nucleolin also contributed to the stabilization of cPLA2α mRNA. | [] | Consistent with the role of nucleolin in the regulation of mRNA stability, we found that nucleolin also contributed to the stabilization of cPLA2α mRNA. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 49 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Since without identical nucleolin-binding site UCCCGA but with HuR-binding element AUUUA is found within the cPLA2α 3′UTR sequence, the effect of nucleolin on the stabilization of cPLA2α mRNA might result from the cooperation of nucleolin with RNA-binding proteins as well as the basal expression of GADD45α mRNA is regu... | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 367 | 43,197 | 1 | false | Since without identical nucleolin-binding site UCCCGA but with HuR-binding element AUUUA is found within the cPLA2α 3′UTR sequence, the effect of nucleolin on the stabilization of cPLA2α mRNA might result from the cooperation of nucleolin with RNA-binding proteins as well as the basal expression of GADD45α mRNA is regu... | [
"49"
] | Since without identical nucleolin-binding site UCCCGA but with HuR-binding element AUUUA is found within the cPLA2α 3′UTR sequence, the effect of nucleolin on the stabilization of cPLA2α mRNA might result from the cooperation of nucleolin with RNA-binding proteins as well as the basal expression of GADD45α mRNA is regu... | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Indeed, we found that RNA-binding protein HuR bound to AUUUA of cPLA2α 3′UTR sequence and enhanced the mRNA stability (our unpublished data). | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 141 | 43,198 | 0 | false | Indeed, we found that RNA-binding protein HuR bound to AUUUA of cPLA2α 3′UTR sequence and enhanced the mRNA stability (our unpublished data). | [] | Indeed, we found that RNA-binding protein HuR bound to AUUUA of cPLA2α 3′UTR sequence and enhanced the mRNA stability (our unpublished data). | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | Although PMA had no effect on the stabilization of cPLA2α mRNA, our data showed that nucleolin was also involved in the regulation of PMA-induced transcriptional activation of cPLA2α gene. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 188 | 43,199 | 0 | false | Although PMA had no effect on the stabilization of cPLA2α mRNA, our data showed that nucleolin was also involved in the regulation of PMA-induced transcriptional activation of cPLA2α gene. | [] | Although PMA had no effect on the stabilization of cPLA2α mRNA, our data showed that nucleolin was also involved in the regulation of PMA-induced transcriptional activation of cPLA2α gene. | true | true | true | true | true | 7,477 |
1 | DISCUSSION | 1 | 26–29 | [
"B26 B27 B28 B29",
"B23",
"B30",
"B44",
"B45",
"B46",
"B47",
"B48",
"B49"
] | 18,025,046 | pmid-9201969|pmid-11375391|pmid-9988766|pmid-10867029|pmid-9525925|pmid-15689183|pmid-8381049|pmid-10978317|pmid-11479288|pmid-8940164|pmid-7800505|pmid-15548519|pmid-15322111|pmid-10749741|pmid-7800505|pmid-8148385|pmid-11559711|pmid-11042196|pmid-15540987|pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-1... | These results revealed that nucleolin plays dual functions of transcriptional and post-transcriptional activity in the regulation of cPLA2α gene. | [
"26–29",
"23",
"30",
"44",
"45",
"46",
"47",
"48",
"49"
] | 145 | 43,200 | 0 | false | These results revealed that nucleolin plays dual functions of transcriptional and post-transcriptional activity in the regulation of cPLA2α gene. | [] | These results revealed that nucleolin plays dual functions of transcriptional and post-transcriptional activity in the regulation of cPLA2α gene. | true | true | true | true | true | 7,477 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | It is known that the motif (U/G)CCCG(A/G) is responsible for the binding of nucleolin to RNA (39). | [
"39",
"50",
"51",
"52",
"39"
] | 98 | 43,201 | 1 | false | It is known that the motif (U/G)CCCG(A/G) is responsible for the binding of nucleolin to RNA. | [
"39"
] | It is known that the motif (U/G)CCCG(A/G) is responsible for the binding of nucleolin to RNA. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | However, we found that the binding of nucleolin to the GC-rich Sp1 site within cPLA2α promoter was in an Sp1-independent manner. | [
"39",
"50",
"51",
"52",
"39"
] | 128 | 43,202 | 0 | false | However, we found that the binding of nucleolin to the GC-rich Sp1 site within cPLA2α promoter was in an Sp1-independent manner. | [] | However, we found that the binding of nucleolin to the GC-rich Sp1 site within cPLA2α promoter was in an Sp1-independent manner. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Thus, nucleolin might gain access to DNA through two pathways. | [
"39",
"50",
"51",
"52",
"39"
] | 62 | 43,203 | 0 | false | Thus, nucleolin might gain access to DNA through two pathways. | [] | Thus, nucleolin might gain access to DNA through two pathways. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | First, since Sp1 siRNA had no effect on the binding of nucleolin to Sp1 element, indicating that nucleolin might directly bind to DNA and recruit c-Jun transcriptional factor to Sp1 sites and then activate gene expression. | [
"39",
"50",
"51",
"52",
"39"
] | 222 | 43,204 | 0 | false | First, since Sp1 siRNA had no effect on the binding of nucleolin to Sp1 element, indicating that nucleolin might directly bind to DNA and recruit c-Jun transcriptional factor to Sp1 sites and then activate gene expression. | [] | First, since Sp1 siRNA had no effect on the binding of nucleolin to Sp1 element, indicating that nucleolin might directly bind to DNA and recruit c-Jun transcriptional factor to Sp1 sites and then activate gene expression. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 50 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Nucleolin is a matrix attachment region (MAR)-binding protein to provide a link between DNA and nuclear matrix scaffolding (50). | [
"39",
"50",
"51",
"52",
"39"
] | 128 | 43,205 | 1 | false | Nucleolin is a matrix attachment region (MAR)-binding protein to provide a link between DNA and nuclear matrix scaffolding. | [
"50"
] | Nucleolin is a matrix attachment region (MAR)-binding protein to provide a link between DNA and nuclear matrix scaffolding. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | In addition, nucleolin was also found to bind to the NFκB DNA-binding motif and the KLF2 promoter (51,52). | [
"39",
"50",
"51",
"52",
"39"
] | 106 | 43,206 | 0 | false | In addition, nucleolin was also found to bind to the NFκB DNA-binding motif and the KLF2 promoter. | [
"51,52"
] | In addition, nucleolin was also found to bind to the NFκB DNA-binding motif and the KLF2 promoter. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Thus, nucleolin may interact with DNA and other transcriptional factors, such as c-Jun, to regulate transcription. | [
"39",
"50",
"51",
"52",
"39"
] | 114 | 43,207 | 0 | false | Thus, nucleolin may interact with DNA and other transcriptional factors, such as c-Jun, to regulate transcription. | [] | Thus, nucleolin may interact with DNA and other transcriptional factors, such as c-Jun, to regulate transcription. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | It is very interesting to note that whether the binding of nucleolin to GC-rich Sp1 site has the sequence specificity. | [
"39",
"50",
"51",
"52",
"39"
] | 118 | 43,208 | 0 | false | It is very interesting to note that whether the binding of nucleolin to GC-rich Sp1 site has the sequence specificity. | [] | It is very interesting to note that whether the binding of nucleolin to GC-rich Sp1 site has the sequence specificity. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Contrary to the binding of nucleolin to cPLA2α promoter, we found that SV40 promoter containing Sp1-binding sites was not regulated by nucleolin. | [
"39",
"50",
"51",
"52",
"39"
] | 145 | 43,209 | 0 | false | Contrary to the binding of nucleolin to cPLA2α promoter, we found that SV40 promoter containing Sp1-binding sites was not regulated by nucleolin. | [] | Contrary to the binding of nucleolin to cPLA2α promoter, we found that SV40 promoter containing Sp1-binding sites was not regulated by nucleolin. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Furthermore, we also found that the interaction between nucleolin and Sp1-binding site was not occurred in all Sp1-regulated promoters such as gastrin. | [
"39",
"50",
"51",
"52",
"39"
] | 151 | 43,210 | 0 | false | Furthermore, we also found that the interaction between nucleolin and Sp1-binding site was not occurred in all Sp1-regulated promoters such as gastrin. | [] | Furthermore, we also found that the interaction between nucleolin and Sp1-binding site was not occurred in all Sp1-regulated promoters such as gastrin. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | It is possible that the nucleotide sequence surrounding the AGCCC and UCCCGA can modulate the interaction of nucleolin with DNA and RNA (39), respectively. | [
"39",
"50",
"51",
"52",
"39"
] | 155 | 43,211 | 1 | false | It is possible that the nucleotide sequence surrounding the AGCCC and UCCCGA can modulate the interaction of nucleolin with DNA and RNA, respectively. | [
"39"
] | It is possible that the nucleotide sequence surrounding the AGCCC and UCCCGA can modulate the interaction of nucleolin with DNA and RNA, respectively. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Second, access of nucleolin to cPLA2α promoter may also skip from direct binding but be bridged by other factors to DNA. | [
"39",
"50",
"51",
"52",
"39"
] | 120 | 43,212 | 0 | false | Second, access of nucleolin to cPLA2α promoter may also skip from direct binding but be bridged by other factors to DNA. | [] | Second, access of nucleolin to cPLA2α promoter may also skip from direct binding but be bridged by other factors to DNA. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | Although there was no effect of Sp1 siRNA on nucleolin binding, we could not rule out the possibility that the binding of nucleolin to DNA might have occurred concomitant with Sp1-like proteins binding. | [
"39",
"50",
"51",
"52",
"39"
] | 202 | 43,213 | 0 | false | Although there was no effect of Sp1 siRNA on nucleolin binding, we could not rule out the possibility that the binding of nucleolin to DNA might have occurred concomitant with Sp1-like proteins binding. | [] | Although there was no effect of Sp1 siRNA on nucleolin binding, we could not rule out the possibility that the binding of nucleolin to DNA might have occurred concomitant with Sp1-like proteins binding. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | In addition, in spite of nucleolin and Sp1 bound to DNA was dependent on Sp1-binding sites, the binding of Sp1 to DNA was in a nucleolin-independent manner. | [
"39",
"50",
"51",
"52",
"39"
] | 156 | 43,214 | 0 | false | In addition, in spite of nucleolin and Sp1 bound to DNA was dependent on Sp1-binding sites, the binding of Sp1 to DNA was in a nucleolin-independent manner. | [] | In addition, in spite of nucleolin and Sp1 bound to DNA was dependent on Sp1-binding sites, the binding of Sp1 to DNA was in a nucleolin-independent manner. | true | true | true | true | true | 7,478 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B50",
"B51",
"B52",
"B39"
] | 18,025,046 | pmid-10973489|pmid-12954631|pmid-10506225|pmid-11262397|pmid-10544174|pmid-9108024|pmid-8676391|pmid-7799955|pmid-16025516|pmid-16571724|pmid-8676391 | These results suggested that Sp1/c-Jun and nucleolin/c-Jun complexes could together or independently bind to Sp1-binding sites and regulate PMA-induced transcriptional activation of cPLA2α gene. | [
"39",
"50",
"51",
"52",
"39"
] | 194 | 43,215 | 0 | false | These results suggested that Sp1/c-Jun and nucleolin/c-Jun complexes could together or independently bind to Sp1-binding sites and regulate PMA-induced transcriptional activation of cPLA2α gene. | [] | These results suggested that Sp1/c-Jun and nucleolin/c-Jun complexes could together or independently bind to Sp1-binding sites and regulate PMA-induced transcriptional activation of cPLA2α gene. | true | true | true | true | true | 7,478 |
3 | DISCUSSION | 1 | 7 | [
"B7",
"B41",
"B47",
"B53"
] | 18,025,046 | pmid-9169405|pmid-15033900|pmid-16698799|pmid-12138209 | In conclusion, we have identified the functional interaction between c-Jun, nucleolin and Sp1 to mediate cPLA2α expression in PMA signal-activated human tumor cells. | [
"7",
"41",
"47",
"53"
] | 165 | 43,216 | 0 | false | In conclusion, we have identified the functional interaction between c-Jun, nucleolin and Sp1 to mediate cPLA2α expression in PMA signal-activated human tumor cells. | [] | In conclusion, we have identified the functional interaction between c-Jun, nucleolin and Sp1 to mediate cPLA2α expression in PMA signal-activated human tumor cells. | true | true | true | true | true | 7,479 |
3 | DISCUSSION | 1 | 7 | [
"B7",
"B41",
"B47",
"B53"
] | 18,025,046 | pmid-9169405|pmid-15033900|pmid-16698799|pmid-12138209 | Our results demonstrate that the activation of the PMA signaling pathway leads to the binding of c-Jun/nucleolin and c-Jun/Sp1 complexes to the cPLA2α promoter, resulting in the transcriptional activation of cPLA2α gene. | [
"7",
"41",
"47",
"53"
] | 220 | 43,217 | 0 | false | Our results demonstrate that the activation of the PMA signaling pathway leads to the binding of c-Jun/nucleolin and c-Jun/Sp1 complexes to the cPLA2α promoter, resulting in the transcriptional activation of cPLA2α gene. | [] | Our results demonstrate that the activation of the PMA signaling pathway leads to the binding of c-Jun/nucleolin and c-Jun/Sp1 complexes to the cPLA2α promoter, resulting in the transcriptional activation of cPLA2α gene. | true | true | true | true | true | 7,479 |
3 | DISCUSSION | 1 | 7 | [
"B7",
"B41",
"B47",
"B53"
] | 18,025,046 | pmid-9169405|pmid-15033900|pmid-16698799|pmid-12138209 | Based on the expression of cPLA2α is critical for transformed growth of NSCLC and tumorigenesis (7,41), our study suggested that nucleolin, in addition to contribute to the process of tumor development by linking to major tumor suppressors, Rb and p53 (47,53), could associate with transcription factor c-Jun and up-regu... | [
"7",
"41",
"47",
"53"
] | 403 | 43,218 | 0 | false | Based on the expression of cPLA2α is critical for transformed growth of NSCLC and tumorigenesis, our study suggested that nucleolin, in addition to contribute to the process of tumor development by linking to major tumor suppressors, Rb and p53, could associate with transcription factor c-Jun and up-regulate cPLA2α exp... | [
"7,41",
"47,53"
] | Based on the expression of cPLA2α is critical for transformed growth of NSCLC and tumorigenesis, our study suggested that nucleolin, in addition to contribute to the process of tumor development by linking to major tumor suppressors, Rb and p53, could associate with transcription factor c-Jun and up-regulate cPLA2α exp... | true | true | true | true | true | 7,479 |
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