Estrogen Receptor Beta (ERβ): A Ligand Activated Tumor Suppressor

Estrogen receptor alpha (ERα) and estrogen receptor beta (ERβ) belong to a superfamily of nuclear receptors called steroid hormone receptors, which, upon binding ligand, dimerize and translocate to the nucleus where they activate or repress the transcription of a large number of genes, thus modulati...

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Main Authors: Rahul Mal, Alexa Magner, Joel David, Jharna Datta, Meghna Vallabhaneni, Mahmoud Kassem, Jasmine Manouchehri, Natalie Willingham, Daniel Stover, Jeffery Vandeusen, Sagar Sardesai, Nicole Williams, Robert Wesolowski, Maryam Lustberg, Ramesh K. Ganju, Bhuvaneswari Ramaswamy, Mathew A. Cherian
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-10-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2020.587386/full
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author Rahul Mal
Alexa Magner
Joel David
Jharna Datta
Meghna Vallabhaneni
Mahmoud Kassem
Mahmoud Kassem
Jasmine Manouchehri
Natalie Willingham
Daniel Stover
Daniel Stover
Jeffery Vandeusen
Jeffery Vandeusen
Sagar Sardesai
Sagar Sardesai
Nicole Williams
Nicole Williams
Robert Wesolowski
Robert Wesolowski
Maryam Lustberg
Maryam Lustberg
Ramesh K. Ganju
Bhuvaneswari Ramaswamy
Bhuvaneswari Ramaswamy
Mathew A. Cherian
Mathew A. Cherian
author_facet Rahul Mal
Alexa Magner
Joel David
Jharna Datta
Meghna Vallabhaneni
Mahmoud Kassem
Mahmoud Kassem
Jasmine Manouchehri
Natalie Willingham
Daniel Stover
Daniel Stover
Jeffery Vandeusen
Jeffery Vandeusen
Sagar Sardesai
Sagar Sardesai
Nicole Williams
Nicole Williams
Robert Wesolowski
Robert Wesolowski
Maryam Lustberg
Maryam Lustberg
Ramesh K. Ganju
Bhuvaneswari Ramaswamy
Bhuvaneswari Ramaswamy
Mathew A. Cherian
Mathew A. Cherian
author_sort Rahul Mal
collection DOAJ
description Estrogen receptor alpha (ERα) and estrogen receptor beta (ERβ) belong to a superfamily of nuclear receptors called steroid hormone receptors, which, upon binding ligand, dimerize and translocate to the nucleus where they activate or repress the transcription of a large number of genes, thus modulating critical physiologic processes. ERβ has multiple isoforms that show differing association with prognosis. Expression levels of the full length ERβ1 isoform are often lower in aggressive cancers as compared to normal tissue. High ERβ1 expression is associated with improved overall survival in women with breast cancer. The promise of ERβ activation, as a potential targeted therapy, is based on concurrent activation of multiple tumor suppressor pathways with few side effects compared to chemotherapy. Thus, ERβ is a nuclear receptor with broad-spectrum tumor suppressor activity, which could serve as a potential treatment target in a variety of human cancers including breast cancer. Further development of highly selective agonists that lack ERα agonist activity, will be necessary to fully harness the potential of ERβ.
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spelling doaj.art-e10d89465998455496bb1a64694d5fae2022-12-22T00:22:48ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2020-10-011010.3389/fonc.2020.587386587386Estrogen Receptor Beta (ERβ): A Ligand Activated Tumor SuppressorRahul Mal0Alexa Magner1Joel David2Jharna Datta3Meghna Vallabhaneni4Mahmoud Kassem5Mahmoud Kassem6Jasmine Manouchehri7Natalie Willingham8Daniel Stover9Daniel Stover10Jeffery Vandeusen11Jeffery Vandeusen12Sagar Sardesai13Sagar Sardesai14Nicole Williams15Nicole Williams16Robert Wesolowski17Robert Wesolowski18Maryam Lustberg19Maryam Lustberg20Ramesh K. Ganju21Bhuvaneswari Ramaswamy22Bhuvaneswari Ramaswamy23Mathew A. Cherian24Mathew A. Cherian25Comprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesStefanie Spielman Comprehensive Breast Cancer, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesStefanie Spielman Comprehensive Breast Cancer, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesStefanie Spielman Comprehensive Breast Cancer, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesStefanie Spielman Comprehensive Breast Cancer, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesStefanie Spielman Comprehensive Breast Cancer, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesStefanie Spielman Comprehensive Breast Cancer, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesStefanie Spielman Comprehensive Breast Cancer, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesStefanie Spielman Comprehensive Breast Cancer, The Ohio State University, Columbus, OH, United StatesComprehensive Cancer Center, The Ohio State University, Columbus, OH, United StatesStefanie Spielman Comprehensive Breast Cancer, The Ohio State University, Columbus, OH, United StatesEstrogen receptor alpha (ERα) and estrogen receptor beta (ERβ) belong to a superfamily of nuclear receptors called steroid hormone receptors, which, upon binding ligand, dimerize and translocate to the nucleus where they activate or repress the transcription of a large number of genes, thus modulating critical physiologic processes. ERβ has multiple isoforms that show differing association with prognosis. Expression levels of the full length ERβ1 isoform are often lower in aggressive cancers as compared to normal tissue. High ERβ1 expression is associated with improved overall survival in women with breast cancer. The promise of ERβ activation, as a potential targeted therapy, is based on concurrent activation of multiple tumor suppressor pathways with few side effects compared to chemotherapy. Thus, ERβ is a nuclear receptor with broad-spectrum tumor suppressor activity, which could serve as a potential treatment target in a variety of human cancers including breast cancer. Further development of highly selective agonists that lack ERα agonist activity, will be necessary to fully harness the potential of ERβ.https://www.frontiersin.org/articles/10.3389/fonc.2020.587386/fullESR1ESR2ERαERβbreast cancer
spellingShingle Rahul Mal
Alexa Magner
Joel David
Jharna Datta
Meghna Vallabhaneni
Mahmoud Kassem
Mahmoud Kassem
Jasmine Manouchehri
Natalie Willingham
Daniel Stover
Daniel Stover
Jeffery Vandeusen
Jeffery Vandeusen
Sagar Sardesai
Sagar Sardesai
Nicole Williams
Nicole Williams
Robert Wesolowski
Robert Wesolowski
Maryam Lustberg
Maryam Lustberg
Ramesh K. Ganju
Bhuvaneswari Ramaswamy
Bhuvaneswari Ramaswamy
Mathew A. Cherian
Mathew A. Cherian
Estrogen Receptor Beta (ERβ): A Ligand Activated Tumor Suppressor
Frontiers in Oncology
ESR1
ESR2
ERα
ERβ
breast cancer
title Estrogen Receptor Beta (ERβ): A Ligand Activated Tumor Suppressor
title_full Estrogen Receptor Beta (ERβ): A Ligand Activated Tumor Suppressor
title_fullStr Estrogen Receptor Beta (ERβ): A Ligand Activated Tumor Suppressor
title_full_unstemmed Estrogen Receptor Beta (ERβ): A Ligand Activated Tumor Suppressor
title_short Estrogen Receptor Beta (ERβ): A Ligand Activated Tumor Suppressor
title_sort estrogen receptor beta erβ a ligand activated tumor suppressor
topic ESR1
ESR2
ERα
ERβ
breast cancer
url https://www.frontiersin.org/articles/10.3389/fonc.2020.587386/full
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