中华肿瘤杂志
中華腫瘤雜誌
중화종류잡지
CHINESE JOURNAL OF ONCOLOGY
2009年
6期
418-422
,共5页
张卫东%韩轶鹏%宗志红%郭健%李明江%王旭晖
張衛東%韓軼鵬%宗誌紅%郭健%李明江%王旭暉
장위동%한질붕%종지홍%곽건%리명강%왕욱휘
唑来膦酸%肺肿瘤%细胞周期%凋亡
唑來膦痠%肺腫瘤%細胞週期%凋亡
서래련산%폐종류%세포주기%조망
Zoledronic acid%Lung neoplasms%Cell cycle%Apoptosis
目的 研究唑来膦酸对肺癌95D细胞的细胞周期阻滞及诱导凋亡作用.方法 采用二苯基溴化四氮唑蓝法检测唑来膦酸对肺癌95D细胞增殖的影响;采用流式细胞仪检测唑来瞵酸作用后肺癌95D细胞的细胞周期和凋亡的变化,并在光镜和电镜下观察细胞凋亡的形态变化;采用Western blot和逆转录聚合酶链反应检测唑来膦酸对肺癌95D细胞凋亡相关基因ERK1/ERK2、bcl-2、bax和survivin表达水平的影响.结果 唑来膦酸对肺癌95D细胞的增殖抑制作用呈时间和浓度依赖性,94.0% μmol/L唑来膦酸作用6 d时,抑制率达89.8%.随着唑来膦酸作用时间的延长,G1期细胞数量增多,G2期和S期细胞减少,凋亡细胞的数最逐渐增多.光镜和电镜均观察到细胞出现了相应的凋亡形态学变化.细胞凋亡相关基因ERK、bcl-2和survivin的表达水平下降,bax的表达水平增高.结论 唑来膦酸对肺癌95D细胞的细胞周期有阻滞作用,并能诱导其凋亡.
目的 研究唑來膦痠對肺癌95D細胞的細胞週期阻滯及誘導凋亡作用.方法 採用二苯基溴化四氮唑藍法檢測唑來膦痠對肺癌95D細胞增殖的影響;採用流式細胞儀檢測唑來瞵痠作用後肺癌95D細胞的細胞週期和凋亡的變化,併在光鏡和電鏡下觀察細胞凋亡的形態變化;採用Western blot和逆轉錄聚閤酶鏈反應檢測唑來膦痠對肺癌95D細胞凋亡相關基因ERK1/ERK2、bcl-2、bax和survivin錶達水平的影響.結果 唑來膦痠對肺癌95D細胞的增殖抑製作用呈時間和濃度依賴性,94.0% μmol/L唑來膦痠作用6 d時,抑製率達89.8%.隨著唑來膦痠作用時間的延長,G1期細胞數量增多,G2期和S期細胞減少,凋亡細胞的數最逐漸增多.光鏡和電鏡均觀察到細胞齣現瞭相應的凋亡形態學變化.細胞凋亡相關基因ERK、bcl-2和survivin的錶達水平下降,bax的錶達水平增高.結論 唑來膦痠對肺癌95D細胞的細胞週期有阻滯作用,併能誘導其凋亡.
목적 연구서래련산대폐암95D세포적세포주기조체급유도조망작용.방법 채용이분기추화사담서람법검측서래련산대폐암95D세포증식적영향;채용류식세포의검측서래린산작용후폐암95D세포적세포주기화조망적변화,병재광경화전경하관찰세포조망적형태변화;채용Western blot화역전록취합매련반응검측서래련산대폐암95D세포조망상관기인ERK1/ERK2、bcl-2、bax화survivin표체수평적영향.결과 서래련산대폐암95D세포적증식억제작용정시간화농도의뢰성,94.0% μmol/L서래련산작용6 d시,억제솔체89.8%.수착서래련산작용시간적연장,G1기세포수량증다,G2기화S기세포감소,조망세포적수최축점증다.광경화전경균관찰도세포출현료상응적조망형태학변화.세포조망상관기인ERK、bcl-2화survivin적표체수평하강,bax적표체수평증고.결론 서래련산대폐암95D세포적세포주기유조체작용,병능유도기조망.
Objective To study the effect of zoledronic acid on cell cycle blocking and induction of apoptosis in lung cancer cell line 95D cells, and their mechanisms of action. Methods The effect of zoledronic acid (ZOL) on proliferation of lung cancer cell line 95D cells was observed by MTT assay. Cell cycle and apoptosis of the lung cancer cells was examined by flow cytometry. The apoptosis in the cancer cells was also examined by light and transmission electron microscopy. The expressions of ERK, Bcl-2, Bax and survivin were measured by Western blot and RT-PCR. Results ZOL showed inhibitory effect on the proliferation of lung cancer cells in vitro, in a time-dependant and a dose-dependant manner. With time extending after ZOL treatment, the number of apoptosis cells was increased. The expression of ERK, Bcl-2 and survivin was down-regulated and that of Bax up-regulated. Conclusion Zoledronic acid can block the cell cycle and induce apoptosis in lung cancer cells in vitro.