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PBRM1 Regulates Stress Response in Epithelial Cells

Polybromo1 (PBRM1) is a chromatin remodeler subunit highly mutated in cancer, particularly clear cell renal carcinoma. PBRM1 is a member of the SWI/SNF subcomplex, PBAF (PBRM1-Brg1/Brm-associated factors), and is characterized by six tandem bromodomains. Here we establish a role for PBRM1 in epithel...

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Autores principales: Porter, Elizabeth G., Dhiman, Alisha, Chowdhury, Basudev, Carter, Benjamin C., Lin, Hang, Stewart, Jane C., Kazemian, Majid, Wendt, Michael K., Dykhuizen, Emily C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514269/
https://www.ncbi.nlm.nih.gov/pubmed/31077944
http://dx.doi.org/10.1016/j.isci.2019.04.027
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author Porter, Elizabeth G.
Dhiman, Alisha
Chowdhury, Basudev
Carter, Benjamin C.
Lin, Hang
Stewart, Jane C.
Kazemian, Majid
Wendt, Michael K.
Dykhuizen, Emily C.
author_facet Porter, Elizabeth G.
Dhiman, Alisha
Chowdhury, Basudev
Carter, Benjamin C.
Lin, Hang
Stewart, Jane C.
Kazemian, Majid
Wendt, Michael K.
Dykhuizen, Emily C.
author_sort Porter, Elizabeth G.
collection PubMed
description Polybromo1 (PBRM1) is a chromatin remodeler subunit highly mutated in cancer, particularly clear cell renal carcinoma. PBRM1 is a member of the SWI/SNF subcomplex, PBAF (PBRM1-Brg1/Brm-associated factors), and is characterized by six tandem bromodomains. Here we establish a role for PBRM1 in epithelial cell maintenance through the expression of genes involved in cell adhesion, metabolism, stress response, and apoptosis. In support of a general role for PBRM1 in stress response and apoptosis, we observe that loss of PBRM1 results in an increase in reactive oxygen species generation and a decrease in cellular viability under stress conditions. We find that loss of PBRM1 promotes cell growth under favorable conditions but is required for cell survival under conditions of cellular stress.
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spelling pubmed-65142692019-05-20 PBRM1 Regulates Stress Response in Epithelial Cells Porter, Elizabeth G. Dhiman, Alisha Chowdhury, Basudev Carter, Benjamin C. Lin, Hang Stewart, Jane C. Kazemian, Majid Wendt, Michael K. Dykhuizen, Emily C. iScience Article Polybromo1 (PBRM1) is a chromatin remodeler subunit highly mutated in cancer, particularly clear cell renal carcinoma. PBRM1 is a member of the SWI/SNF subcomplex, PBAF (PBRM1-Brg1/Brm-associated factors), and is characterized by six tandem bromodomains. Here we establish a role for PBRM1 in epithelial cell maintenance through the expression of genes involved in cell adhesion, metabolism, stress response, and apoptosis. In support of a general role for PBRM1 in stress response and apoptosis, we observe that loss of PBRM1 results in an increase in reactive oxygen species generation and a decrease in cellular viability under stress conditions. We find that loss of PBRM1 promotes cell growth under favorable conditions but is required for cell survival under conditions of cellular stress. Elsevier 2019-04-26 /pmc/articles/PMC6514269/ /pubmed/31077944 http://dx.doi.org/10.1016/j.isci.2019.04.027 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Porter, Elizabeth G.
Dhiman, Alisha
Chowdhury, Basudev
Carter, Benjamin C.
Lin, Hang
Stewart, Jane C.
Kazemian, Majid
Wendt, Michael K.
Dykhuizen, Emily C.
PBRM1 Regulates Stress Response in Epithelial Cells
title PBRM1 Regulates Stress Response in Epithelial Cells
title_full PBRM1 Regulates Stress Response in Epithelial Cells
title_fullStr PBRM1 Regulates Stress Response in Epithelial Cells
title_full_unstemmed PBRM1 Regulates Stress Response in Epithelial Cells
title_short PBRM1 Regulates Stress Response in Epithelial Cells
title_sort pbrm1 regulates stress response in epithelial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514269/
https://www.ncbi.nlm.nih.gov/pubmed/31077944
http://dx.doi.org/10.1016/j.isci.2019.04.027
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