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Divergent features of ERβ isoforms in triple negative breast cancer: progress and implications for further research
Estrogen receptor β (ERβ) was discovered more than 20 years ago. However, the extent and role of ERβ expression in breast cancer remain controversial, especially in the context of triple-negative breast cancer (TNBC). ERβ exists as multiple isoforms, and a series of studies has revealed an inconsist...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626554/ https://www.ncbi.nlm.nih.gov/pubmed/37936981 http://dx.doi.org/10.3389/fcell.2023.1240386 |
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author | Yan, Shunchao Wang, Jinpeng Chen, Hong Zhang, Duo Imam, Murshid |
author_facet | Yan, Shunchao Wang, Jinpeng Chen, Hong Zhang, Duo Imam, Murshid |
author_sort | Yan, Shunchao |
collection | PubMed |
description | Estrogen receptor β (ERβ) was discovered more than 20 years ago. However, the extent and role of ERβ expression in breast cancer remain controversial, especially in the context of triple-negative breast cancer (TNBC). ERβ exists as multiple isoforms, and a series of studies has revealed an inconsistent role of ERβ isoforms in TNBC. Our recent results demonstrated contrasting functions of ERβ1 and ERβ2/β5 in TNBC. Additional research should be conducted to explore the functions of individual ERβ isoforms and develop targeted drugs according to the relevant mechanisms. Consequently, a systematic review of ERβ isoforms is necessary. In this review, we overview the structure of ERβ isoforms and detail what is known about the function of ERβ isoforms in normal mammary tissue and breast cancer. Moreover, this review highlights the divergent features of ERβ isoforms in TNBC. This review also provides insights into the implications of targeting ERβ isoforms for clinical treatment. In conclusion, this review provides a framework delineating the roles and mechanisms of different ERβ isoforms in TNBC and sheds light on future directions for basic and clinical research. |
format | Online Article Text |
id | pubmed-10626554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106265542023-11-07 Divergent features of ERβ isoforms in triple negative breast cancer: progress and implications for further research Yan, Shunchao Wang, Jinpeng Chen, Hong Zhang, Duo Imam, Murshid Front Cell Dev Biol Cell and Developmental Biology Estrogen receptor β (ERβ) was discovered more than 20 years ago. However, the extent and role of ERβ expression in breast cancer remain controversial, especially in the context of triple-negative breast cancer (TNBC). ERβ exists as multiple isoforms, and a series of studies has revealed an inconsistent role of ERβ isoforms in TNBC. Our recent results demonstrated contrasting functions of ERβ1 and ERβ2/β5 in TNBC. Additional research should be conducted to explore the functions of individual ERβ isoforms and develop targeted drugs according to the relevant mechanisms. Consequently, a systematic review of ERβ isoforms is necessary. In this review, we overview the structure of ERβ isoforms and detail what is known about the function of ERβ isoforms in normal mammary tissue and breast cancer. Moreover, this review highlights the divergent features of ERβ isoforms in TNBC. This review also provides insights into the implications of targeting ERβ isoforms for clinical treatment. In conclusion, this review provides a framework delineating the roles and mechanisms of different ERβ isoforms in TNBC and sheds light on future directions for basic and clinical research. Frontiers Media S.A. 2023-10-23 /pmc/articles/PMC10626554/ /pubmed/37936981 http://dx.doi.org/10.3389/fcell.2023.1240386 Text en Copyright © 2023 Yan, Wang, Chen, Zhang and Imam. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Yan, Shunchao Wang, Jinpeng Chen, Hong Zhang, Duo Imam, Murshid Divergent features of ERβ isoforms in triple negative breast cancer: progress and implications for further research |
title | Divergent features of ERβ isoforms in triple negative breast cancer: progress and implications for further research |
title_full | Divergent features of ERβ isoforms in triple negative breast cancer: progress and implications for further research |
title_fullStr | Divergent features of ERβ isoforms in triple negative breast cancer: progress and implications for further research |
title_full_unstemmed | Divergent features of ERβ isoforms in triple negative breast cancer: progress and implications for further research |
title_short | Divergent features of ERβ isoforms in triple negative breast cancer: progress and implications for further research |
title_sort | divergent features of erβ isoforms in triple negative breast cancer: progress and implications for further research |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626554/ https://www.ncbi.nlm.nih.gov/pubmed/37936981 http://dx.doi.org/10.3389/fcell.2023.1240386 |
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