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前列腺癌治疗的表观遗传影响知识。

Knowledge of epigenetic influence for prostate cancer therapy.

作者信息

Watanabe Masatoshi, Takagi Akimitsu, Matsuzaki Takeshi, Kami Daisuke, Toyota Minoru, Hirokawa Yoshifumi, Shiraishi Taizo

机构信息

Laboratory for Medical Engineering, Division of Materials Science and Chemical Engineering, Graduate School of Engineering, Yokohama National University, Yokohama, Japan.

出版信息

Curr Cancer Drug Targets. 2006 Sep;6(6):533-51. doi: 10.2174/156800906778194568.

Abstract

Prostate cancer is one of the most prevalent cancers in men in many countries, increasing in frequency with age through the most advanced years. The standard treatment for newly diagnosed metastatic tumors is androgen ablation. However, advanced prostate cancer nevertheless often develops in many cases. Although hormonal manipulation and chemotherapy have uncertain value for advanced lesions, especially androgen-independent, recent studies of docetaxel-based chemotherapy in men with androgen-independent prostate cancer have shown a survival benefit. Intensive investigations have shown that aberrant epigenetic features. including aberrant DNA methylation, make an important contribution to carcinogenesis as well as genetic alterations. Hypermethylation of CpG islands in promoter regions can lead to silencing of tumor-suppressor genes, while hypomethylation of the genome leads to instability. This review attempts to provide up-to-date information regarding the significance of epigenetics for human prostate cancer, with aberrations offering dues to therapy and possibly also providing targets for anticancer drugs.

摘要

前列腺癌是许多国家男性中最常见的癌症之一,随着年龄增长,其发病率在高龄阶段不断上升。新诊断出的转移性肿瘤的标准治疗方法是雄激素去除疗法。然而,在许多情况下,晚期前列腺癌仍会经常发生。尽管激素治疗和化疗对晚期病变,尤其是雄激素非依赖性病变的价值尚不确定,但最近针对雄激素非依赖性前列腺癌男性患者进行的基于多西他赛的化疗研究显示出了生存获益。深入研究表明,异常的表观遗传特征,包括异常的DNA甲基化,对致癌作用以及基因改变都有重要影响。启动子区域CpG岛的高甲基化可导致肿瘤抑制基因沉默,而基因组的低甲基化则会导致基因组不稳定。本综述旨在提供有关表观遗传学对人类前列腺癌意义的最新信息,这些异常可为治疗提供线索,也可能为抗癌药物提供靶点。

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