[1]曲凯,林婷,魏吉超,等.Cisplatin induces cell cycle arrest and senescence via upregulating P53 and P21 expression in HepG2 cells[J].南方医科大学学报,2013,(09):1253.
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Cisplatin induces cell cycle arrest and senescence via upregulating P53 and P21 expression in HepG2 cells()
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《南方医科大学学报》[ISSN:1673-4254/CN:44-1627/R]

卷:
期数:
2013年09期
页码:
1253
栏目:
出版日期:
2013-09-15

文章信息/Info

Title:
顺铂通过调控P53及P21表达水平影响HepG2细胞衰老及周期阻滞
作者:
曲凯; 林婷; 魏吉超; 孟凡迪; 王志鑫; 黄子超; 万永; 宋思冬; 刘司南; 常虎林; 董亚峰; 刘昌
关键词:
顺铂; 肝癌; 细胞衰老; P53; P21
Keywords:
cisplatin;  cellular senescence;  hepatocellular carcinoma;  P53;  P21
摘要:
目的化疗药物能够通过诱导肿瘤细胞衰老从而发挥治疗效果。顺铂作为最常用的化疗药物能否诱导肝癌细胞发生加速
性衰老目前尚不清楚。方法使用MTT法和克隆形成试验检测不同剂量顺铂对HepG2细胞增殖的影响；分别用流式细胞仪及
衰老相关β-半乳糖苷酶染色检测细胞周期及衰老情况；RT-PCR检测TP53、P21及P19基因的mRNA表达水平，Western blotting
检测P53和P21蛋白表达水平。结果顺铂能够诱导HepG2细胞出现不可逆的生长停滞及细胞周期阻滞。2.0 μg/ml顺铂作用
于HepG2后衰老相关β-半乳糖苷酶染色阳性，并呈现时间依赖性。在顺铂诱导衰老过程中，P19基因表达水平升高，在诱导48 h
后达到峰值后逐渐下降，而P53和P21表达水平则持续升高。结论本研究提示顺铂能够诱导肝癌细胞出现衰老样表型，这一结
果为进一步探讨其抗肝癌机制提供了基础。
Abstract:
Objective Cellular senescence as one of the important steps against tumor is observed in many cancer patients
receiving chemotherapy and is related to chemotherapeutic response. To investigate the effect of cisplatin on hepatocellular
carcinoma, we treated HepG2 cells exhibiting wild-type TP53 with gradient concentrations of cisplatin. Methods The
inhibitory effects of cisplatin on human hepatoma HepG2 cells were detected by MTT assay and colony formation test. The
changes in cell cycle were analyzed by flow cytometry, and cellular senescence was detected with senescence associated
β-galactosidase (SA β-gal) staining. The relative mRNA expression levels of TP53, P21 and P19 was estimated using
semi-quantitative real-time RT-PCR, and the protein expressions of P53 and P21 were detected using Western blotting. Results
Cisplatin induced irreversible proliferation inhibition and G1 phase arrest of HepG2 cells. Elevated levels of
senescence-associated β-galactosidase was observed in HepG2 cells exposed to low doses of cisplatin. P19 expression
immediately increased following cisplatin exposure and reached the maximum level at 48 h, followed then by a rapid decrease
to the baseline level, whereas the expressions levels of TP53 and P21 mRNA increased continuously. Western blotting
confirmed P53 and P21 expression changes similar to their mRNA expressions during cisplatin-induced cellular senescence in
HepG2 cells. Conclusion Our results revealed a functional link between cisplatin and hepatocellular senescence. Cellular
senescence induced by cisplatin as a stabile senescent cellular model can be used for further research.

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更新日期/Last Update: 1900-01-01