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PROTACs:克服耐药性的表观遗传策略的有前途的方法。

PROTACs: Promising Approaches for Epigenetic Strategies to Overcome Drug Resistance.

机构信息

Department of Microbiology and Immunology, Weill Cornell Medicine, 1300 York Ave, Box 62, New York, NY, United States.

Department of Biochemistry, Weill Cornell Medicine, 1300 York Ave, Box 63, New York, NY, 10065, United States.

出版信息

Curr Cancer Drug Targets. 2021;21(4):306-325. doi: 10.2174/1568009621666210203110857.

Abstract

Epigenetic modulation of gene expression is essential for tissue-specific development and maintenance in mammalian cells. Disruption of epigenetic processes, and the subsequent alteration of gene functions, can result in inappropriate activation or inhibition of various cellular signaling pathways, leading to cancer. Recent advancements in the understanding of the role of epigenetics in cancer initiation and progression have uncovered functions for DNA methylation, histone modifications, nucleosome positioning, and non-coding RNAs. Epigenetic therapies have shown some promise for hematological malignancies, and a wide range of epigenetic-based drugs are undergoing clinical trials. However, in a dynamic survival strategy, cancer cells exploit their heterogeneous population which frequently results in the rapid acquisition of therapy resistance. Here, we describe novel approaches in drug discovery targeting the epigenome, highlighting recent advances the selective degradation of target proteins using Proteolysis Targeting Chimera (PROTAC) to address drug resistance.

摘要

基因表达的表观遗传调控对于哺乳动物细胞的组织特异性发育和维持至关重要。表观遗传过程的破坏,以及随后基因功能的改变,可能导致各种细胞信号通路的异常激活或抑制,从而导致癌症。最近对表观遗传学在癌症发生和进展中的作用的理解揭示了 DNA 甲基化、组蛋白修饰、核小体定位和非编码 RNA 的功能。表观遗传疗法在血液恶性肿瘤方面显示出一定的前景,并且正在进行广泛的基于表观遗传的药物临床试验。然而,在动态的生存策略中,癌细胞利用其异质性群体,这经常导致治疗耐药性的迅速获得。在这里,我们描述了针对表观基因组的药物发现的新方法,重点介绍了使用蛋白水解靶向嵌合体 (PROTAC) 选择性降解靶蛋白以解决耐药性的最新进展。

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