Suppr超能文献

DNA损伤药物诱导的Bcl-2下调对于高危型人乳头瘤病毒阳性的喉癌细胞系(HEp-2)和口腔表皮样癌细胞系(KB)凋亡的诱导至关重要。

DNA damaging drugs-induced down-regulation of Bcl-2 is essential for induction of apoptosis in high-risk HPV-positive HEp-2 and KB cells.

作者信息

Singh Sandeep, Chhipa Rishi Raj, Vijayakumar Maleppillil Vavachan, Bhat Manoj Kumar

机构信息

National Centre for Cell Science, NCCS Complex, Ganeshkhind, Pune 411 007, India.

出版信息

Cancer Lett. 2006 May 18;236(2):213-21. doi: 10.1016/j.canlet.2005.05.024. Epub 2005 Jul 5.

Abstract

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.

摘要

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。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验