实用医学杂志
實用醫學雜誌
실용의학잡지
THE JOURNAL OF PRACTICAL MEDICINE
2014年
4期
511-514
,共4页
林淑慧%谢国柱%张静芳%蔡小慧%姚奇伟%孙权权%王玮%袁亚维
林淑慧%謝國柱%張靜芳%蔡小慧%姚奇偉%孫權權%王瑋%袁亞維
림숙혜%사국주%장정방%채소혜%요기위%손권권%왕위%원아유
乳腺肿瘤%坎地沙坦%细胞周期阻滞%凋亡%p53%Survivin
乳腺腫瘤%坎地沙坦%細胞週期阻滯%凋亡%p53%Survivin
유선종류%감지사탄%세포주기조체%조망%p53%Survivin
Breast carcinoma%Candesartan%Cell cycle arrest%Apoptosis%p53%Survivin
目的:探讨血管紧张素Ⅱ1型受体(AT1R)拮抗剂坎地沙坦对人乳腺癌细胞系 MCF-7的生长抑制作用,为AT1R拮抗剂在乳腺癌中的应用提供实验依据。方法:噻唑蓝(MTT)比色法检测坎地沙坦对乳腺癌胞MCF-7细胞的生长抑制率,计算半数抑制浓度(IC50)。流式细胞仪分析坎地沙坦对MCF-7细胞周期和凋亡的影响。Western blot检测经坎地沙坦处理前后MCF-7细胞中野生型p53、survivin的蛋白表达差异。结果:坎地沙坦能够显著抑制乳腺癌细胞 MCF-7的增殖,使细胞凋亡显著增强,促使细胞发生 G1期周期阻滞,减小了S期细胞比例,上调其野生型p53和下调survivin蛋白表达水平。结论:坎地沙坦在体外抑制MCF-7细胞生长,诱导细胞发生周期阻滞和凋亡,机制可能与其调节p53、survivin蛋白的表达有关。
目的:探討血管緊張素Ⅱ1型受體(AT1R)拮抗劑坎地沙坦對人乳腺癌細胞繫 MCF-7的生長抑製作用,為AT1R拮抗劑在乳腺癌中的應用提供實驗依據。方法:噻唑藍(MTT)比色法檢測坎地沙坦對乳腺癌胞MCF-7細胞的生長抑製率,計算半數抑製濃度(IC50)。流式細胞儀分析坎地沙坦對MCF-7細胞週期和凋亡的影響。Western blot檢測經坎地沙坦處理前後MCF-7細胞中野生型p53、survivin的蛋白錶達差異。結果:坎地沙坦能夠顯著抑製乳腺癌細胞 MCF-7的增殖,使細胞凋亡顯著增彊,促使細胞髮生 G1期週期阻滯,減小瞭S期細胞比例,上調其野生型p53和下調survivin蛋白錶達水平。結論:坎地沙坦在體外抑製MCF-7細胞生長,誘導細胞髮生週期阻滯和凋亡,機製可能與其調節p53、survivin蛋白的錶達有關。
목적:탐토혈관긴장소Ⅱ1형수체(AT1R)길항제감지사탄대인유선암세포계 MCF-7적생장억제작용,위AT1R길항제재유선암중적응용제공실험의거。방법:새서람(MTT)비색법검측감지사탄대유선암포MCF-7세포적생장억제솔,계산반수억제농도(IC50)。류식세포의분석감지사탄대MCF-7세포주기화조망적영향。Western blot검측경감지사탄처리전후MCF-7세포중야생형p53、survivin적단백표체차이。결과:감지사탄능구현저억제유선암세포 MCF-7적증식,사세포조망현저증강,촉사세포발생 G1기주기조체,감소료S기세포비례,상조기야생형p53화하조survivin단백표체수평。결론:감지사탄재체외억제MCF-7세포생장,유도세포발생주기조체화조망,궤제가능여기조절p53、survivin단백적표체유관。
Objective To investigate the proliferation inhibition of angiotensin Ⅱ 1 receptor (AT1R) antagonist candesartan on human breast cancer cell line MCF-7. Methods MCF-7 cells were tested in vitro for cytotoxicity of candesartan with MTT method. The effect of candesartan on cell cycle and apoptosis of MCF-7 cells were evaluated by flow cytometry. Western Blot was applied to test the expression level of wild-type p53 and Survivin protein. Results After candesartan treatment, a dose- and time-dependent decreased proliferation in MCF-7 cells was observed. Induction of G1 cell cycle arrest and increased apoptosis in MCF-7 cells were also observed.Western blot assay showed that candesartan up-regulated wild-type P53 expression and down-regulated the Survivin expression in MCF-7 cells. Conclusions This study suggests that candesartan could inhibit the proliferation , induce G1 cell cycle arrest and apoptosis of MCF-7cellsby regulating the protein expression level of gene p53 and Survivin.