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表观遗传学癌症疗法:概念验证和遗留挑战。

Epigenetic cancer therapy: Proof of concept and remaining challenges.

机构信息

Global Drug Discovery, Research and Development, Bayer Schering Pharma, Berlin, Germany.

出版信息

Bioessays. 2010 Nov;32(11):949-57. doi: 10.1002/bies.201000061.

Abstract

Over the past few years several drugs that target epigenetic modifications have shown clinical benefits, thus seemingly validating epigenetic cancer therapy. More recently, however, it has become clear that these drugs are either characterized by low specificity or that their target enzymes have low substrate specificity. As such, clinical proof-of-concept for epigenetic cancer therapies remains to be established. Human cancers are characterized by widespread changes in their genomic DNA methylation and histone modification patterns. Epigenetic cancer therapy aims to restore normal epigenetic modification patterns through the inhibition of epigenetic modifier enzymes. In this review, we provide an overview about the known functional roles of DNA methyltransferases, histone deacetylases, histone methyltransferases, and demethylases in cancer development. The available data identify several examples that warrant further consideration as drug targets. Future research should be directed toward targeted enzyme inhibition and toward exploring interactions between epigenetic pathways to maximize cancer specificity.

摘要

在过去的几年中,几种针对表观遗传修饰的药物已经显示出了临床益处,从而似乎验证了表观遗传学癌症治疗的有效性。然而,最近人们已经清楚地认识到,这些药物要么特异性低,要么它们的靶酶对底物的特异性低。因此,表观遗传学癌症治疗的临床概念验证仍然有待建立。人类癌症的特点是基因组 DNA 甲基化和组蛋白修饰模式的广泛改变。表观遗传学癌症治疗旨在通过抑制表观遗传修饰酶来恢复正常的表观遗传修饰模式。在这篇综述中,我们概述了 DNA 甲基转移酶、组蛋白去乙酰化酶、组蛋白甲基转移酶和去甲基酶在癌症发展中的已知功能作用。现有的数据确定了几个值得进一步考虑作为药物靶点的例子。未来的研究应该针对靶向酶抑制以及探索表观遗传途径之间的相互作用,以最大限度地提高癌症的特异性。

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