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Polycomb group proteins in cancer: multifaceted functions and strategies for modulation. | LitMetric

Polycomb group proteins in cancer: multifaceted functions and strategies for modulation.

NAR Cancer

Department of Medicinal Chemistry and Molecular Pharmacology, College of Pharmacy, Purdue University and Purdue University Center for Cancer Research, 201 S. University St., West Lafayette, IN 47907 USA.

Published: December 2021

AI Article Synopsis

  • Polycomb repressive complexes (PRCs) are diverse protein complexes crucial for regulating gene expression during development and often mis-regulated in cancer.
  • PRCs are divided into PRC1, which has histone ubiquitin ligase activity, and PRC2, which has histone methyltransferase activity, though the specific functions of the different PRC1 variations are still being explored.
  • Understanding how PRCs work and their role in cancer could lead to improved therapies by identifying precise targets within these complexes.

Article Abstract

Polycomb repressive complexes (PRCs) are a heterogenous collection of dozens, if not hundreds, of protein complexes composed of various combinations of subunits. PRCs are transcriptional repressors important for cell-type specificity during development, and as such, are commonly mis-regulated in cancer. PRCs are broadly characterized as PRC1 with histone ubiquitin ligase activity, or PRC2 with histone methyltransferase activity; however, the mechanism by which individual PRCs, particularly the highly diverse set of PRC1s, alter gene expression has not always been clear. Here we review the current understanding of how PRCs act, both individually and together, to establish and maintain gene repression, the biochemical contribution of individual PRC subunits, the mis-regulation of PRC function in different cancers, and the current strategies for modulating PRC activity. Increased mechanistic understanding of PRC function, as well as cancer-specific roles for individual PRC subunits, will uncover better targets and strategies for cancer therapies.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8489530PMC
http://dx.doi.org/10.1093/narcan/zcab039DOI Listing

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