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Polycomb-like Proteins in Gene Regulation and Cancer

Polycomb-like proteins (PCLs) are a crucial group of proteins associated with the Polycomb repressive complex 2 (PRC2) and are responsible for setting up the PRC2.1 subcomplex. In the vertebrate system, three homologous PCLs exist: PHF1 (PCL1), MTF2 (PCL2), and PHF19 (PCL3). Although the PCLs share...

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Detalles Bibliográficos
Autores principales: Fischer, Sabrina, Liefke, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137883/
https://www.ncbi.nlm.nih.gov/pubmed/37107696
http://dx.doi.org/10.3390/genes14040938
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author Fischer, Sabrina
Liefke, Robert
author_facet Fischer, Sabrina
Liefke, Robert
author_sort Fischer, Sabrina
collection PubMed
description Polycomb-like proteins (PCLs) are a crucial group of proteins associated with the Polycomb repressive complex 2 (PRC2) and are responsible for setting up the PRC2.1 subcomplex. In the vertebrate system, three homologous PCLs exist: PHF1 (PCL1), MTF2 (PCL2), and PHF19 (PCL3). Although the PCLs share a similar domain composition, they differ significantly in their primary sequence. PCLs play a critical role in targeting PRC2.1 to its genomic targets and regulating the functionality of PRC2. However, they also have PRC2-independent functions. In addition to their physiological roles, their dysregulation has been associated with various human cancers. In this review, we summarize the current understanding of the molecular mechanisms of the PCLs and how alterations in their functionality contribute to cancer development. We particularly highlight the nonoverlapping and partially opposing roles of the three PCLs in human cancer. Our review provides important insights into the biological significance of the PCLs and their potential as therapeutic targets for cancer treatment.
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spelling pubmed-101378832023-04-28 Polycomb-like Proteins in Gene Regulation and Cancer Fischer, Sabrina Liefke, Robert Genes (Basel) Review Polycomb-like proteins (PCLs) are a crucial group of proteins associated with the Polycomb repressive complex 2 (PRC2) and are responsible for setting up the PRC2.1 subcomplex. In the vertebrate system, three homologous PCLs exist: PHF1 (PCL1), MTF2 (PCL2), and PHF19 (PCL3). Although the PCLs share a similar domain composition, they differ significantly in their primary sequence. PCLs play a critical role in targeting PRC2.1 to its genomic targets and regulating the functionality of PRC2. However, they also have PRC2-independent functions. In addition to their physiological roles, their dysregulation has been associated with various human cancers. In this review, we summarize the current understanding of the molecular mechanisms of the PCLs and how alterations in their functionality contribute to cancer development. We particularly highlight the nonoverlapping and partially opposing roles of the three PCLs in human cancer. Our review provides important insights into the biological significance of the PCLs and their potential as therapeutic targets for cancer treatment. MDPI 2023-04-18 /pmc/articles/PMC10137883/ /pubmed/37107696 http://dx.doi.org/10.3390/genes14040938 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Fischer, Sabrina
Liefke, Robert
Polycomb-like Proteins in Gene Regulation and Cancer
title Polycomb-like Proteins in Gene Regulation and Cancer
title_full Polycomb-like Proteins in Gene Regulation and Cancer
title_fullStr Polycomb-like Proteins in Gene Regulation and Cancer
title_full_unstemmed Polycomb-like Proteins in Gene Regulation and Cancer
title_short Polycomb-like Proteins in Gene Regulation and Cancer
title_sort polycomb-like proteins in gene regulation and cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137883/
https://www.ncbi.nlm.nih.gov/pubmed/37107696
http://dx.doi.org/10.3390/genes14040938
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