摘要
目的:探讨节律基因hClock、hBmal1对胃癌细胞SGC-7901化疗敏感性的影响。方法:体外持续黑暗条件下培养SGC-7901,用实时定量PCR法检测两种主要的节律基因hClock、hBmal1在SGC-7901中不同时间点的表达,分别在节律基因hClock、hBmal1表达的高峰及低谷给予化疗药物多西他赛,CCK-8法检测化疗药物对肿瘤细胞的抑制率。结果:实时定量CR结果显示节律基因hClock、hBmal1在胃癌细胞SGC-7901中不同时间点表达不同,存在时相性波动,表达高峰在20:00,而表达低谷在08:00。CCK-8法显示在节律基因hClock、hBmal1表达高峰时,多西他赛对肿瘤细胞的抑制率低于其在低谷时的抑制率。结论:节律基因hClock、hBmal1过表达可以降低胃癌细胞SGC-7901对多西他赛的敏感性。
SGC-7901 cells were cultivated under continuous darkness in vitro.The expression levels of the two main circadian genes hClock and hBmall at the different time were determined by real-time polymerase chain reaction（PCR）. Docetaxel was administered at the peak and nadir time point respectively. The inhibition of SGC-7901 cell proliferation was measured using a CCK-8 kit. Result： The expression of circadian genes hClock and hBmall varied at different times, as shown by real-time PCR. The expression of circadian genes hClock and hBmall showed Phase oseillation. The maximum expression of hClock and hBmall mRNA was at 20：00. whereas their minimum expression was at 08：00. The inhibition ratio of docetaxel to SGC-7901 cells at the maximum expression of hClock and hBmall genes was lower than that at the minimum expression. Conclusion： Circadian Genes hClock and hBmall can reduce the drug sensitivity of SGC-7901 cell line to docetaxel in vitro.
出处
《中国肿瘤临床》
CAS
CSCD
北大核心
2013年第20期1213-1216,共4页
Chinese Journal of Clinical Oncology
基金
四川省南充市科学技术计划项目(编号:2010SF10)资助~~
