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作为抗癌治疗靶点的凋亡途径缺陷。

Defects of the apoptotic pathway as therapeutic target against cancer.

作者信息

Mashima Tetsuo, Tsuruo Takashi

机构信息

Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo, Japan.

出版信息

Drug Resist Updat. 2005 Dec;8(6):339-43. doi: 10.1016/j.drup.2005.11.001. Epub 2005 Dec 9.

Abstract

Over the past 10 years evidence has been accumulating that antitumour agents induce apoptosis in cancer cells and that abnormalities in apoptosis signaling pathways often occur in cancer cells and are associated with drug resistance. The implication is that factors regulating the apoptotic process play a critical role in tumour sensitivity to chemotherapy, and hence may be rational molecular targets for novel antitumour agents. Significantly, oncogenic signals make cancer cells intrinsically more susceptible to apoptosis; defects in the pathway occur subsequent to cancer development. Important emerging questions are the pattern of alterations in the apoptotic pathway in a particular tumour (cell) and the best strategy to exploit them and induce selective tumour cell death. Here, we review recent progress in this field.

摘要

在过去的10年里,越来越多的证据表明,抗肿瘤药物可诱导癌细胞凋亡,且凋亡信号通路的异常常常发生在癌细胞中,并与耐药性相关。这意味着,调节凋亡过程的因素在肿瘤对化疗的敏感性中起关键作用,因此可能是新型抗肿瘤药物合理的分子靶点。值得注意的是,致癌信号使癌细胞本质上更易发生凋亡;该通路的缺陷在癌症发展之后出现。重要的新问题是特定肿瘤(细胞)中凋亡通路的改变模式,以及利用这些改变并诱导选择性肿瘤细胞死亡的最佳策略。在此,我们综述该领域的最新进展。

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