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作 者:刘哲[1] 张媛媛[1] 张倩文[1] 钟浩[1] 孙小锦 蒋琛琛[1] 蒋志文[1] 刘浩[1]
机构地区:[1]蚌埠医学院药学系安徽省生化药物工程技术研究中心,安徽蚌埠233030
出 处:《蚌埠医学院学报》2014年第1期22-25,29,共5页Journal of Bengbu Medical College
基 金:国家自然科学基金资助项目(81000992;81072207);安徽省教育厅自然科学研究资助项目(KJ2012A201)
摘 要:目的:研究3-溴丙酮酸(3-BrPA)联合阿霉素(ADM)对乳腺癌细胞MDA-MB-231增殖及凋亡的影响。方法:采用3-BrPA 80、160、320μmol/L作用于MDA-MB-231乳腺癌细胞18 h后,测定其对细胞内ATP的影响;分别用3-BrPA 10、20、40、80、160μmol/L和ADM 0.75、1.5、3、6、12μmol/L,以及3-BrPA 80μmol/L与ADM 0.75、1.5、3、6、12μmol/L合用作用于MDA-MB-231乳腺癌细胞24、48和72 h后,MTT法检测乳腺癌细胞MDA-MB-231增殖情况;3-BrPA 80μmol/L组、ADM0.75μmol/L组以及3-BrPA 80μmol/L与ADM 0.75μmol/L合用组作用于乳腺癌细胞MDA-Mb-231 24 h后,利用碘化丙啶染色,流式细胞仪检测其诱导乳腺癌细胞凋亡的影响;采用3-BrPA 16μmol/L、ADM 0.2μmol/L以及3-BrPA 16μmol/L与ADM0.2μmol/L合用作用于乳腺癌细胞MDA-MB-231,5 d后观察对集落克隆形成的影响。结果:3-BrPA对乳腺癌细胞MDA-MB-231 ATP的生成有抑制作用;3-BrPA联合ADM后可明显增强ADM的细胞毒性作用;3-BrPA 80μmol/L与ADM 0.75μmol/L合用组诱导乳腺癌细胞MDA-MB-231 24 h凋亡率为39.6%,均显著高于对照组、3-BrPA单用组和ADM单用组(P<0.01);3-BrPA增强ADM对乳腺癌细胞MDA-MB-231集落克隆形成的抑制作用。结论:3-BrPA可以增强ADM对乳腺癌细胞MDAMB-231增殖的抑制作用以及增强ADM诱导乳腺癌细胞凋亡的作用。Objective: To investigate the effect of 3-Bromopyruvate (3-BrPA) combined with adriamycin ( ADM ) on proliferation and apoptosis of human breast carcinoma cells in vitro. Methods:The effects of 3-BrPA at 80,160 and 320μ mol/L on ATP production of MDA-MB-231 breast cancer cells were detected. The growth inhibition effect was detected by MTT assay which induced by 3-BrPA( 10, 20,40,80,160 p.mol/L) , adriamycin(0. 75,1.5,3,6,12 μmol/L) and 3-BrPA at 80 p, mol/L combined with adriamycin(0. 75,1.5, 3,6,12 μmol/L) for 24 h,48 h and 72 h in MDA-MB-231 breast cancer cells. Cells were treated with 3-BrPA(80 μ mol/L) , adriamyein(0.75 μmoL/L) and 3-BrPA(80 Ixmol/L) combined with adriamycin(0.75 μmol/L) for 24 hours,the apoptotic cells were detected using propidium iodide staining by flow cytometry. Cells were treated with 3-BrPA ( 16 μmol/L) , adriamycin ( 0.2 μmol/L) and 3-BrPA( 16 μmol/L) combined with adriamycin (0. 5 μmol/L) for 5 days, the colony formation was detected by crystal violet staining method. Results:3-BrPA inhibited the formation of ATP in MDA-MB-231 breast cancer cells;3-BrPA combined with ADM significantly enhanced the eytotoxieity of ADM. When MDA-MB-231 breast cancer ceils were treated with 3-BrPA at 80 μmol/L combined with ADM at 0.75 μmol/L, the apoptosis rate was 39.6% ,which was significantly higher than that in control group,3-BrPA group and ADM group(P 〈0.01). 3-BrPA enhanced the inhibitory effect of ADM on colony formation of MDA-MB-231 breast cancer cells. Conclusions :3-BrPA can enhance the inhibitory effect of adriamycin on proliferation and apoptosis of MDA-MB-231 breast cancer cells.
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