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Regulation of apoptosis in prostate cancer

机译:治疗前列腺癌中凋亡

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摘要

Transformation and malignant progression of prostate cancer is regulated by the inability of prostatic epithelial cells to undergo apoptosis rather than by increased cell proliferation. The basic apoptotic machinery of most prostate cancer cells is intact and the inability to undergo apoptosis is due to molecular alterations that result in failure to initiate or execute apoptotic pathways. This review discusses the role of anti-apoptotic proteins such as BcI-2/BcIxl, NF-kB, IGF, caveolin, and Akt, and pro-apoptotic molecules such as PTEN, p53, Binl, TGF-p and Par-4 that can regulate progression of prostate cancer. In addition to highlighting the salient features of these molecules and their relevance in apoptosis, this review provides an appraisal of their therapeutic potential in prostate cancer. Molecular targeting of these proteins and/or then" innate pro- or anti-apoptotic pathways, either singly or in combination, may be explored in conjunction with conventional and currently available experimental strategies for the treatment of both hormone-sensitive arid hormone-resistant prostate cancer.
机译:前列腺癌的转化和恶性进展是通过前列腺上皮细胞进行细胞凋亡而不是通过增加的细胞增殖来调节。大多数前列腺癌细胞的基本凋亡机械完整,并且无法进行细胞凋亡是由于分子改变导致未发生或执行凋亡途径。本综述讨论了抗凋亡蛋白如BCI-2 / BCix1,NF-KB,IGF,Caveolin和Akt,以及促凋亡分子,如PTEN,P53,Bin1,TGF-P 和PAR-4这可以调节前列腺癌的进展。除了突出这些分子的显着特征及其在凋亡中的相关性之外,该评论还提供了对前列腺癌的治疗潜力的评估。这些蛋白质和/或然后“单独或组合的先天蛋白或抗凋亡途径的分子靶向可以与常规和目前可用的实验策略一起探索,用于治疗激素敏感的干旱激素抗性前列腺癌症。

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