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PBRM1 Regulates the Stress Response in Epithelial Cells

32 Pages Posted: 2 Oct 2018 Publication Status: Published

See all articles by Elizabeth G. Porter

Elizabeth G. Porter

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

Alisha Dhiman

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

Basudev Chowdhury

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

Benjamin C. Carter

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

Hang Lin

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

Jane C. Stewart

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

Majid Kazemian

Purdue University - Department of Biochemistry

Michael K. Wendt

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

Emily Dykhuizen

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

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Abstract

Polybromo1 (PBRM1) is a chromatin remodeler subunit highly mutated in cancer, particularly renal clear cell 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.

Suggested Citation

Porter, Elizabeth G. and Dhiman, Alisha and Chowdhury, Basudev and Carter, Benjamin C. and Lin, Hang and Stewart, Jane C. and Kazemian, Majid and Wendt, Michael K. and Dykhuizen, Emily, PBRM1 Regulates the Stress Response in Epithelial Cells (September 25, 2018). Available at SSRN: https://ssrn.com/abstract=3254909 or http://dx.doi.org/10.2139/ssrn.3254909
This version of the paper has not been formally peer reviewed.

Elizabeth G. Porter

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

610 Purdue Mall
West Lafayette, IN 47907
United States

Alisha Dhiman

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

610 Purdue Mall
West Lafayette, IN 47907
United States

Basudev Chowdhury

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

610 Purdue Mall
West Lafayette, IN 47907
United States

Benjamin C. Carter

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

610 Purdue Mall
West Lafayette, IN 47907
United States

Hang Lin

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

610 Purdue Mall
West Lafayette, IN 47907
United States

Jane C. Stewart

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

610 Purdue Mall
West Lafayette, IN 47907
United States

Majid Kazemian

Purdue University - Department of Biochemistry

610 Purdue Mall
West Lafayette, IN 47907
United States

Michael K. Wendt

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology

610 Purdue Mall
West Lafayette, IN 47907
United States

Emily Dykhuizen (Contact Author)

Purdue University - Department of Medicinal Chemistry and Molecular Pharmacology ( email )

610 Purdue Mall
West Lafayette, IN 47907
United States

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