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RUNX3 Meets the Ubiquitin-Proteasome System in Cancer

RUNX3 is a transcription factor with regulatory roles in cell proliferation and development. While largely characterized as a tumor suppressor, RUNX3 can also be oncogenic in certain cancers. Many factors account for the tumor suppressor function of RUNX3, which is reflected by its ability to suppre...

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Autores principales: Toska, Albano, Modi, Nikita, Chen, Lin-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10001085/
https://www.ncbi.nlm.nih.gov/pubmed/36899853
http://dx.doi.org/10.3390/cells12050717
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author Toska, Albano
Modi, Nikita
Chen, Lin-Feng
author_facet Toska, Albano
Modi, Nikita
Chen, Lin-Feng
author_sort Toska, Albano
collection PubMed
description RUNX3 is a transcription factor with regulatory roles in cell proliferation and development. While largely characterized as a tumor suppressor, RUNX3 can also be oncogenic in certain cancers. Many factors account for the tumor suppressor function of RUNX3, which is reflected by its ability to suppress cancer cell proliferation after expression-restoration, and its inactivation in cancer cells. Ubiquitination and proteasomal degradation represent a major mechanism for the inactivation of RUNX3 and the suppression of cancer cell proliferation. On the one hand, RUNX3 has been shown to facilitate the ubiquitination and proteasomal degradation of oncogenic proteins. On the other hand, RUNX3 can be inactivated through the ubiquitin–proteasome system. This review encapsulates two facets of RUNX3 in cancer: how RUNX3 suppresses cell proliferation by facilitating the ubiquitination and proteasomal degradation of oncogenic proteins, and how RUNX3 is degraded itself through interacting RNA-, protein-, and pathogen-mediated ubiquitination and proteasomal degradation.
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spelling pubmed-100010852023-03-11 RUNX3 Meets the Ubiquitin-Proteasome System in Cancer Toska, Albano Modi, Nikita Chen, Lin-Feng Cells Review RUNX3 is a transcription factor with regulatory roles in cell proliferation and development. While largely characterized as a tumor suppressor, RUNX3 can also be oncogenic in certain cancers. Many factors account for the tumor suppressor function of RUNX3, which is reflected by its ability to suppress cancer cell proliferation after expression-restoration, and its inactivation in cancer cells. Ubiquitination and proteasomal degradation represent a major mechanism for the inactivation of RUNX3 and the suppression of cancer cell proliferation. On the one hand, RUNX3 has been shown to facilitate the ubiquitination and proteasomal degradation of oncogenic proteins. On the other hand, RUNX3 can be inactivated through the ubiquitin–proteasome system. This review encapsulates two facets of RUNX3 in cancer: how RUNX3 suppresses cell proliferation by facilitating the ubiquitination and proteasomal degradation of oncogenic proteins, and how RUNX3 is degraded itself through interacting RNA-, protein-, and pathogen-mediated ubiquitination and proteasomal degradation. MDPI 2023-02-24 /pmc/articles/PMC10001085/ /pubmed/36899853 http://dx.doi.org/10.3390/cells12050717 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
Toska, Albano
Modi, Nikita
Chen, Lin-Feng
RUNX3 Meets the Ubiquitin-Proteasome System in Cancer
title RUNX3 Meets the Ubiquitin-Proteasome System in Cancer
title_full RUNX3 Meets the Ubiquitin-Proteasome System in Cancer
title_fullStr RUNX3 Meets the Ubiquitin-Proteasome System in Cancer
title_full_unstemmed RUNX3 Meets the Ubiquitin-Proteasome System in Cancer
title_short RUNX3 Meets the Ubiquitin-Proteasome System in Cancer
title_sort runx3 meets the ubiquitin-proteasome system in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10001085/
https://www.ncbi.nlm.nih.gov/pubmed/36899853
http://dx.doi.org/10.3390/cells12050717
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