中文摘要：

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。

英文摘要：

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.