摘要
目的顺铂(DDP)为广谱抗癌药物,本研究探讨其对MCF-7乳腺癌细胞DNA损伤的作用,并研究其引起细胞凋亡的机制。方法采用DDP(0、2、4、6、8、10 mg·L^(-1))处理乳腺癌MCF-7细胞48 h,MTT法检测顺铂对细胞活性的抑制作用,并计算IC_(50);Western blot检测DNA断裂形成的标志分子γ-H2AX及直接感受DNA双链断裂(DSBs)的分子ATM、细胞凋亡信号分子cleaved caspase-3及凋亡相关的蛋白钙蛋白酶calpain的表达。结果 DDP呈浓度依赖性抑制细胞MCF-7活性,IC_(50)为7.57 mg·L^(-1);与对照组(未采用顺铂处理)相比,顺铂处理组MCF-7细胞内γ-H2AX、ATM、cleaved caspase-3、calpain的表达量增多。结论 DDP可抑制乳腺癌MCF-7细胞的活性,其机制与促进MCF-7细胞凋亡,诱导DNA双链断裂,上调促凋亡相关蛋白有关。
Aim Toinvestigatethemechanismsof DNA damage of cisplatin(DDP),a broad spectrum an-ticancer drug on breast cancer MCF-7 cells and to stud-y the mechanism of apoptosis induced by DDP.Meth-ods MCF-7cellsweretreatedbyDDP(0,2,4,6,8, 10 mg·L-1 )for 48 h.MTT assay was used to detect the inhibitory effect of DDP on MCF-7 cells,and IC50 value was calculated.Western blot was adopted to de-tect the expression ofγ-H2AX,which was the marker of DNA double stranded breaks(DSBs)and ATM(sen-sory molecules of DSBs ),the apoptotic signal trans-duction molecule cleaved caspase-3 ,and the proteins associatedwithapoptosis:calpain.Results DDPin-hibited MCF-7 cell activity in a concentration-depend-ent manner and IC50 was 7. 57 mg·L-1 .In contrast to the control group (without DDP treatment),MCF-7 cells with DDP treatment group expressed more γ-H2AX,ATM,cleaved caspase-3 and calpain.Conclu-sions DDPcouldinhibittheactivityofbreastcancer MCF-7 cells.Its mechanisms may be associated with inhibition of MCF-7 cell apoptosis,induction of DNA double strand breaking and the expression of pro-apop-totic protein up-regulating.
出处
《中国药理学通报》
CAS
CSCD
北大核心
2017年第3期334-337,共4页
Chinese Pharmacological Bulletin
基金
国家自然科学基金资助项目(No 30600753
81172154)
湖南省自然科学基金面上项目(No 2016JJ2088)
湖南省教育厅资助项目(No 13C541)
湖南省中医药管理局资助项目(No 2015123)