Singh Sandeep, Chhipa Rishi Raj, Vijayakumar Maleppillil Vavachan, Bhat Manoj Kumar
National Centre for Cell Science, NCCS Complex, Ganeshkhind, Pune 411 007, India.
Cancer Lett. 2006 May 18;236(2):213-21. doi: 10.1016/j.canlet.2005.05.024. Epub 2005 Jul 5.
DNA damaging chemotherapeutic agents like carboplatin (Carb) and 5-fluorouracil (5-FU), whose effects are mediated through diverse intracellular targets, induce apoptosis in various cancer cells including human papillomavirus (HPV) positive HEp-2 and KB cells. The present work reports the involvement of Bcl-2 in response to the exposure of HEp-2 and KB cells to Carb or 5-FU. We demonstrate that both these drugs are potent inducers of apoptosis. Apoptosis was preceded by decrease in Bcl-2 protein level accompanied by caspase-9 activation and poly(ADP-ribose) polymerase (PARP) cleavage without altering Bax expression. Further analysis revealed down-regulation of Bcl-2 mRNA as well as protein in drugs treated cells. Ectopic expression of Bcl-2 protected cells against drugs mediated DNA damage-induced apoptosis. Overall, data indicates that genotoxic stress leads to down-regulation of Bcl-2 in HEp-2 and KB cells, which plays a decisive role in the outcome of stress in these cells.
像卡铂(Carb)和5-氟尿嘧啶(5-FU)这样的DNA损伤化疗药物,其作用是通过多种细胞内靶点介导的,可诱导包括人乳头瘤病毒(HPV)阳性的喉癌上皮细胞(HEp-2)和口腔表皮样癌细胞(KB)在内的各种癌细胞发生凋亡。目前的研究报告了Bcl-2在HEp-2和KB细胞暴露于卡铂或5-氟尿嘧啶时所起的作用。我们证明这两种药物都是凋亡的有效诱导剂。凋亡之前,Bcl-2蛋白水平下降,同时伴有半胱天冬酶-9激活和聚(ADP-核糖)聚合酶(PARP)裂解,而Bax表达未改变。进一步分析显示,在药物处理的细胞中,Bcl-2 mRNA以及蛋白均下调。Bcl-2的异位表达可保护细胞免受药物介导的DNA损伤诱导的凋亡。总体而言,数据表明遗传毒性应激导致HEp-2和KB细胞中Bcl-2下调,这在这些细胞的应激结果中起决定性作用。