赖氨酸去甲基化酶的化学生物学。

Current chemical genomics Pub Date : 2011-01-01 Epub Date: 2011-08-22 DOI:10.2174/1875397301005010062
Tom D Heightman
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引用次数: 23

摘要

DNA甲基化和/或组蛋白修饰的异常水平在多种慢性疾病患者中观察到。组蛋白尾部赖氨酸的甲基化是一种关键的修饰,它有助于增加基因表达或抑制,这取决于特定的残基和甲基化程度,而甲基化又由赖氨酸甲基转移酶和去甲基化酶的相互作用控制。靶向这些和其他控制染色质修饰的酶的药物可以调节基因簇的表达,可能比作用于易发生变性的下游生化途径的经典药物提供更高的治疗效果。赖氨酸去甲基酶于2004年首次被发现,作为治疗靶点越来越受到关注。本文综述了赖氨酸去甲基化酶在肿瘤、免疫炎症、代谢紊乱、神经科学、病毒学和再生医学等一系列治疗领域的最新发现,并总结了结构生物学和小分子抑制剂的最新进展,为选择性药物样抑制剂的开发提供了蛋白质家族的可追溯性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Chemical biology of lysine demethylases.

Abnormal levels of DNA methylation and/or histone modifications are observed in patients with a wide variety of chronic diseases. Methylation of lysines within histone tails is a key modification that contributes to increased gene expression or repression depending on the specific residue and degree of methylation, which is in turn controlled by the interplay of lysine methyl transferases and demethylases. Drugs that target these and other enzymes controlling chromatin modifications can modulate the expression of clusters of genes, potentially offering higher therapeutic efficacy than classical agents acting on downstream biochemical pathways that are susceptible to degeneracy. Lysine demethylases, first discovered in 2004, are the subject of increasing interest as therapeutic targets. This review provides an overview of recent findings implicating lysine demethylases in a range of therapeutic areas including oncology, immunoinflammation, metabolic disorders, neuroscience, virology and regenerative medicine, together with a summary of recent advances in structural biology and small molecule inhibitor discovery, supporting the tractability of the protein family for the development of selective druglike inhibitors.

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