首页> 外文期刊>Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences >Protein methyltransferase inhibitors as precision cancer therapeutics: a decade of discovery
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Protein methyltransferase inhibitors as precision cancer therapeutics: a decade of discovery

机译:蛋白质甲基转移酶抑制剂作为精确癌症治疗:十年的发现

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摘要

The protein methyltransferases (PMTs) represent a large class of enzymes that catalyse the methylation of side chain nitrogen atoms of the amino acids lysine or arginine at specific locations along the primary sequence of target proteins. These enzymes play a key role in the spatio-temporal control of gene transcription by performing site-specific methylation of lysine or arginine residues within the histone proteins of chromatin, thus effecting chromatin conformational changes that activate or repress gene transcription. Over the past decade, it has become clear that the dysregulated activity of some PMTs plays an oncogenic role in a number of human cancers. Here we review research of the past decade that has identified specific PMTs as oncogenic drivers of cancers and progress toward the discovery and development of selective, small molecule inhibitors of these enzymes as precision cancer therapeutics.
机译:蛋白质甲基转移酶(PMTS)代表大类酶,其沿靶蛋白的初级序列催化氨基酸赖氨酸或精氨酸的侧链氮原子或精氨酸的甲基化。 这些酶在基因转录的时空控制中发挥着关键作用,通过在染色蛋白的组蛋白蛋白内进行赖氨酸或精氨酸残基进行特异性甲基化,从而实现了激活或抑制基因转录的染色质构象变化。 在过去十年中,已经清楚地发现,一些PMT的失调活性在许多人类癌症中起着致癌作用。 在这里,我们审查了对过去十年的研究,该研究已经确定了特定的PMTS作为癌症的致癌驱动因素以及对这些酶的选择性,小分子抑制剂的发现和开发的进展作为精确癌症治疗方法。

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