UCN-01 suppresses thymidylate synthase gene expression and enhances 5-fluorouracil-induced apoptosis in a sequence-dependent manner

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作者
Hsueh, CT [1 ]
Kelsen, D [1 ]
Schwartz, GK [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Div Solid Tumor Oncol, Gastrointestinal Oncol Res Lab, New York, NY 10021 USA
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R73 [肿瘤学];
学科分类号
100214 ;
摘要
UCN-01, a protein kinase C/cyclin-dependent kinase inhibitor, suppressed thymidylate synthase (TS) protein expression in a dose-dependent manner with near complete suppression at 1 mu m after a 24-h exposure in human gastric cancer cell line SK-GT5. Other protein kinase C/cyclin-dependent kinase inhibitors, including flavopiridol and safingol, had a similar effect on TS protein expression, but to a lesser degree. Moreover, UCN-01 repressed the induction of TS after 5-fluorouracil (FU) exposure by 90-95% and significantly enhanced the induction of apoptosis by FU from 4-8% with either FU or UCN-01 alone to 46 +/- 1% (P < 0.005 versus either single drug, reverse sequence, or the combination) when UCN-01 was given after FU, The effect of UCN-01 on TS was associated with a dose dependent suppression of the E2F-1 protein, a transcriptional activator of TS, Northern blot analysis revealed that TS mRNA levels decreased gradually as the concentration of UCN-01 increased, but that E2F-1 mRNA levels remained relatively unchanged, UCN-O1 may provide a novel way to enhance cellular sensitivity toward FU by means of suppressing TS expression mediated mainly by down-regulation of E2F-1.
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页码:2201 / 2206
页数:6
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