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The Role of HECT E3 Ubiquitin Ligases in Colorectal Cancer

Colorectal cancer (CRC) is estimated to rank as the second reason for cancer-related deaths, and the prognosis of CRC patients remains unsatisfactory. Numerous studies on gastrointestinal cell biology have shown that the E3 ligase-mediated ubiquitination exerts key functions in the pathogenesis of C...

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Detalles Bibliográficos
Autores principales: Sun, Aiqin, Chen, Yifei, Tian, Xianyan, Lin, Qiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953483/
https://www.ncbi.nlm.nih.gov/pubmed/36831013
http://dx.doi.org/10.3390/biomedicines11020478
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author Sun, Aiqin
Chen, Yifei
Tian, Xianyan
Lin, Qiong
author_facet Sun, Aiqin
Chen, Yifei
Tian, Xianyan
Lin, Qiong
author_sort Sun, Aiqin
collection PubMed
description Colorectal cancer (CRC) is estimated to rank as the second reason for cancer-related deaths, and the prognosis of CRC patients remains unsatisfactory. Numerous studies on gastrointestinal cell biology have shown that the E3 ligase-mediated ubiquitination exerts key functions in the pathogenesis of CRC. The homologous to E6-associated protein C-terminus (HECT) family E3 ligases are a major group of E3 enzymes, featured with the presence of a catalytic HECT domain, which participate in multiple cellular processes; thus, alterations in HECT E3 ligases in function or expression are closely related to the occurrence and development of many human malignancies, including—but not limited to—CRC. In this review, we summarize the potential role of HECT E3 ligases in colorectal carcinogenesis and the related underlying molecular mechanism to expand our understanding of their pathological functions. Exploiting specific inhibitors targeting HECT E3 ligases could be a potential therapeutic strategy for CRC therapy in the future.
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spelling pubmed-99534832023-02-25 The Role of HECT E3 Ubiquitin Ligases in Colorectal Cancer Sun, Aiqin Chen, Yifei Tian, Xianyan Lin, Qiong Biomedicines Review Colorectal cancer (CRC) is estimated to rank as the second reason for cancer-related deaths, and the prognosis of CRC patients remains unsatisfactory. Numerous studies on gastrointestinal cell biology have shown that the E3 ligase-mediated ubiquitination exerts key functions in the pathogenesis of CRC. The homologous to E6-associated protein C-terminus (HECT) family E3 ligases are a major group of E3 enzymes, featured with the presence of a catalytic HECT domain, which participate in multiple cellular processes; thus, alterations in HECT E3 ligases in function or expression are closely related to the occurrence and development of many human malignancies, including—but not limited to—CRC. In this review, we summarize the potential role of HECT E3 ligases in colorectal carcinogenesis and the related underlying molecular mechanism to expand our understanding of their pathological functions. Exploiting specific inhibitors targeting HECT E3 ligases could be a potential therapeutic strategy for CRC therapy in the future. MDPI 2023-02-07 /pmc/articles/PMC9953483/ /pubmed/36831013 http://dx.doi.org/10.3390/biomedicines11020478 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
Sun, Aiqin
Chen, Yifei
Tian, Xianyan
Lin, Qiong
The Role of HECT E3 Ubiquitin Ligases in Colorectal Cancer
title The Role of HECT E3 Ubiquitin Ligases in Colorectal Cancer
title_full The Role of HECT E3 Ubiquitin Ligases in Colorectal Cancer
title_fullStr The Role of HECT E3 Ubiquitin Ligases in Colorectal Cancer
title_full_unstemmed The Role of HECT E3 Ubiquitin Ligases in Colorectal Cancer
title_short The Role of HECT E3 Ubiquitin Ligases in Colorectal Cancer
title_sort role of hect e3 ubiquitin ligases in colorectal cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953483/
https://www.ncbi.nlm.nih.gov/pubmed/36831013
http://dx.doi.org/10.3390/biomedicines11020478
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