人卵巢癌细胞凋亡和化疗耐药:夏普是一个决定因素吗?

J Li, H Sasaki, Y L Sheng, D Schneiderman, C W Xiao, F Kotsuji, B K Tsang
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引用次数: 46

摘要

顺铂诱导的卵巢癌上皮细胞凋亡在一定程度上是Xiap表达抑制和Fas/FasL系统上调的结果。这些“细胞死亡”和“细胞存活”基因表达的变化导致caspase-3的激活,以及MDM2和FAK的切割。癌细胞未能维持这些基因表达的平衡,从而导致凋亡细胞死亡,这可能是化疗耐药的一个重要因素。Xiap可能是人类卵巢上皮性癌基因治疗的新靶点,依赖于P53的状态,单独表达Xiap反义或与野生型P53反义结合可能为化疗耐药癌症的治疗提供新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Apoptosis and chemoresistance in human ovarian cancer: is Xiap a determinant?

Cisplatin-induced apoptosis in epithelial ovarian cancer cells is in part a consequence of suppressed Xiap expression and upregulation of the Fas/FasL system. Changes in the expression of these 'cell death' and 'cell survival' genes lead to activation of caspase-3, and cleavage of MDM2 and FAK. Failure of cancer cells to maintain a balance in the expression of these genes in favor of apoptotic cell death may be an important factor of chemoresistance. Xiap may be a novel target for gene therapy of human ovarian epithelial cancer and, dependent on P53 status, expression of Xiap antisense alone or in combination with wild-type P53 sense may offer a new approach for the treatment of the chemoresistant cancer.

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