PROTACs: Promising Approaches for Epigenetic Strategies to Overcome Drug Resistance

被引:8
|
作者
Giardina, Sarah F. [1 ]
Valdambrini, Elena [1 ]
Warren, J. David [2 ]
Barany, Francis [1 ]
机构
[1] Weill Cornell Med, Dept Microbiol & Immunol, 1300 York Ave,Box 62, New York, NY 10065 USA
[2] Weill Cornell Med, Dept Biochem, 1300 York Ave,Box 63, New York, NY 10065 USA
关键词
Cancer; oncology; PROTAC; epigenetics; drug resistance; therapy resistance; HISTONE DEACETYLASE INHIBITORS; C-MYC ONCOPROTEIN; BET BROMODOMAIN INHIBITORS; SMALL-MOLECULE INHIBITORS; TUMOR-SUPPRESSOR GENE; SMALL-CELL CARCINOMA; IN-VIVO; PROTEIN-DEGRADATION; MULTIDRUG-RESISTANCE; SELECTIVE DEGRADATION;
D O I
10.2174/1568009621666210203110857
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:306 / 325
页数:20
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