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组蛋白去乙酰化酶抑制剂在膀胱癌治疗中的潜力。

Potential of histone deacetylase inhibitors for bladder cancer treatment.

机构信息

Department of Urology, Ehime University Graduate School of Medicine, Toon, Ehime 791-0295, Japan.

出版信息

Expert Rev Anticancer Ther. 2011 Jun;11(6):959-65. doi: 10.1586/era.10.230.

Abstract

Bladder cancer incidence increases with age, presumably reflecting a cumulative exposure to carcinogens and ever-increasing life expectancy. While aberrant protein expression due to DNA mutations is an essential step during oncogenesis, one recent interest has been the role of epigenetic changes in regulating bladder tumor development. Because aberrant histone acetylation has been linked to malignant diseases in several cases, histone deacetylase inhibitors have great potential as new anticancer drugs owing to their ability to modulate transcription and induce differentiation and apoptosis. We herein review the current knowledge on epigenetic issues in bladder cancer, particularly regarding histone acetylation, and discuss its implications for understanding the molecular basis and treatment of this disease.

摘要

膀胱癌的发病率随年龄增长而增加,这可能反映了致癌物质的累积暴露和不断延长的预期寿命。虽然由于 DNA 突变导致的异常蛋白表达是肿瘤发生过程中的一个重要步骤,但最近人们对表观遗传变化在调节膀胱癌发展中的作用产生了兴趣。由于异常组蛋白乙酰化已在几种情况下与恶性疾病相关联,组蛋白去乙酰化酶抑制剂由于能够调节转录并诱导分化和凋亡,因此具有作为新型抗癌药物的巨大潜力。本文综述了膀胱癌中表观遗传问题的最新知识,特别是组蛋白乙酰化问题,并讨论了其对理解该疾病的分子基础和治疗的意义。

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