Chemically induced degradation of epigenetic targets

Md Kabir, Xufen Yu, H. Ümit Kaniskan, Jian Jin

Research output: Contribution to journalReview articlepeer-review

3 Scopus citations

Abstract

Proteolysis-targeting chimeras (PROTACs) are heterobifunctional small molecules that induce the ternary complex formation between a protein-of-interest (POI) and an E3 ligase, leading to targeted polyubiquitination and degradation of the POI. Particularly, PROTACs have the distinct advantage of targeting both canonical and noncanonical functions of epigenetic targets over traditional inhibitors, which typically target canonical functions only, resulting in greater therapeutic efficacy. In this review, we methodically analyze published PROTAC degraders of epigenetic writer, reader, and eraser proteins and their in vitro and in vivo effects. We highlight the mechanism of action of these degraders and their advantages in targeting both canonical and noncanonical functions of epigenetic targets in the context of cancer treatment. Furthermore, we present a future outlook for this exciting field. Overall, pharmacological degradation of epigenetic targets has emerged as an effective and attractive strategy to thwart cancer progression and growth.

Original languageEnglish
Pages (from-to)4313-4342
Number of pages30
JournalChemical Society Reviews
Volume52
Issue number13
DOIs
StatePublished - 14 Jun 2023

Fingerprint

Dive into the research topics of 'Chemically induced degradation of epigenetic targets'. Together they form a unique fingerprint.

Cite this