Eliopoulos A G, Kerr D J, Herod J, Hodgkins L, Krajewski S, Reed J C, Young L S
CRC Institute for Cancer Studies, University of Birmingham Medical School, UK.
Oncogene. 1995 Oct 5;11(7):1217-28.
Modulation of apoptosis may influence resistance to chemotherapy and therefore affect the outcome of cancer treatment. Ovarian cancer, one of the most fatal malignancies in women, is often associated with drug resistance but the cellular pathways contributing to this effect remain obscure. We have found that Bcl-2 and p53, two proteins implicated in the control of apoptosis, are frequently expressed in fresh biopsies of primary ovarian carcinoma. Examination of Bcl-2 and p53 protein levels in pairs of cis-platin sensitive and resistant ovarian cell lines demonstrated that the resistant variants over-express Bcl-2 and/or p53, apparently due to progressive expansion of Bcl-2 and/or p53 positive subpopulations during the in vitro development of resistance. Exogenous expression of Bcl-2 or a temperature sensitive mutant p53 (ts p53) in the ovarian cell line A2780 resulted in protection from drug-induced apoptosis and a delay in drug-mediated S-phase arrest. Interestingly, p53 accumulation in response to DNA damage induced by different agents was significantly delayed and reduced in the Bcl-2 transfectants compared to the control A2780 line, suggesting that Bcl-2 may act upstream of the p53 pathway. Similarly, the induction of Bax mRNA and protein was also found to be delayed in the presence of Bcl-2. Overall, our data provide further evidence for cross-talk between Bcl-2, p53 and Bax and suggest that these genes are important determinants of drug-induced apoptosis thereby modulating resistance to chemotherapy.
细胞凋亡的调控可能会影响对化疗的耐药性,进而影响癌症治疗的结果。卵巢癌是女性最致命的恶性肿瘤之一,常与耐药性相关,但导致这种效应的细胞途径仍不清楚。我们发现,参与细胞凋亡调控的两种蛋白质Bcl-2和p53,在原发性卵巢癌的新鲜活检组织中经常表达。对顺铂敏感和耐药的卵巢细胞系中Bcl-2和p53蛋白水平的检测表明,耐药变体过度表达Bcl-2和/或p53,这显然是由于在体外耐药性发展过程中Bcl-2和/或p53阳性亚群的逐渐扩增。在卵巢细胞系A2780中外源性表达Bcl-2或温度敏感型突变体p53(ts p53)可保护细胞免受药物诱导的凋亡,并延迟药物介导的S期阻滞。有趣的是,与对照A2780细胞系相比,Bcl-2转染细胞中对不同药物诱导的DNA损伤的p53积累明显延迟且减少,这表明Bcl-2可能在p53途径的上游起作用。同样,在存在Bcl-2的情况下,Bax mRNA和蛋白的诱导也被发现延迟。总体而言,我们的数据为Bcl-2、p53和Bax之间的相互作用提供了进一步的证据,并表明这些基因是药物诱导凋亡的重要决定因素,从而调节对化疗的耐药性。