Chen L, Zheng S, Willingham M C
Cancer Institute, Zhejiang Medical University, Hangzhou.
Zhonghua Zhong Liu Za Zhi. 1997 Mar;19(2):103-6.
To investigate the mechanism by which taxol induces apoptosis in human breast cancer cells.
Cell morphology, agarose gel electrophoresis, flow cytometry, video time-lapse monitor and Western blot were performed for taxol-induced apoptosis in human breast cancer cells (Bcap 37).
BCap 37 cells treated with taxol (100 nm) underwent the arrests of cell mitosis at metaphase of mitosis and induction of apoptosis. Apoptotic cells demonstrated cell shringkage, condensation and fragmentation of chromosomes. Nuclear DNA of apoptotic cells displayed ladder bands characteristic of internucleosomal DNA fragmentation. The expression of bcl-2, inhibitor of apoptosis, was decreased with modification, while that of bax, inducer of apoptosis, increased only at early stage of the apoptotic pathway and decreased later.
In human breast cancer cells the induction of apoptosis by taxol was closely associated with mitotic arrest of cell cycle, and altered expression of bcl-2 and bax gene, possibly playing an important role in regulating taxol-induced apoptosis.
研究紫杉醇诱导人乳腺癌细胞凋亡的机制。
采用细胞形态学、琼脂糖凝胶电泳、流式细胞术、视频延时监测及蛋白质免疫印迹法,对紫杉醇诱导人乳腺癌细胞(Bcap 37)凋亡进行研究。
用100纳米紫杉醇处理的Bcap 37细胞在有丝分裂中期发生细胞有丝分裂停滞并诱导凋亡。凋亡细胞表现为细胞皱缩、染色体凝聚和断裂。凋亡细胞的核DNA呈现出核小体间DNA断裂特有的梯状条带。凋亡抑制因子bcl-2的表达经修饰后降低,而凋亡诱导因子bax的表达仅在凋亡途径早期增加,随后降低。
在人乳腺癌细胞中,紫杉醇诱导凋亡与细胞周期的有丝分裂停滞以及bcl-2和bax基因表达改变密切相关,可能在调节紫杉醇诱导的凋亡中起重要作用。