PBRM1 loss defines a nonimmunogenic tumor phenotype associated with checkpoint inhibitor resistance in renal carcinoma

PBRM1, encoding for a subunit of the SWI/SNF complex, is the second most frequently mutated gene in clear cell renal cell carcinoma (ccRCC). Here, the authors show that PBRM1 loss reduces IFNγ-mediated signalling resulting in a less immunogenic tumor microenvironment and that PBRM1 mutations correla...

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Main Authors: Xian-De Liu, Wen Kong, Christine B. Peterson, Daniel J. McGrail, Anh Hoang, Xuesong Zhang, Truong Lam, Patrick G. Pilie, Haifeng Zhu, Kathryn E. Beckermann, Scott M. Haake, Sevinj Isgandrova, Margarita Martinez-Moczygemba, Nidhi Sahni, Nizar M. Tannir, Shiaw-Yih Lin, W. Kimryn Rathmell, Eric Jonasch
Format: Article
Language:English
Published: Nature Portfolio 2020-05-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-020-15959-6
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author Xian-De Liu
Wen Kong
Christine B. Peterson
Daniel J. McGrail
Anh Hoang
Xuesong Zhang
Truong Lam
Patrick G. Pilie
Haifeng Zhu
Kathryn E. Beckermann
Scott M. Haake
Sevinj Isgandrova
Margarita Martinez-Moczygemba
Nidhi Sahni
Nizar M. Tannir
Shiaw-Yih Lin
W. Kimryn Rathmell
Eric Jonasch
author_facet Xian-De Liu
Wen Kong
Christine B. Peterson
Daniel J. McGrail
Anh Hoang
Xuesong Zhang
Truong Lam
Patrick G. Pilie
Haifeng Zhu
Kathryn E. Beckermann
Scott M. Haake
Sevinj Isgandrova
Margarita Martinez-Moczygemba
Nidhi Sahni
Nizar M. Tannir
Shiaw-Yih Lin
W. Kimryn Rathmell
Eric Jonasch
author_sort Xian-De Liu
collection DOAJ
description PBRM1, encoding for a subunit of the SWI/SNF complex, is the second most frequently mutated gene in clear cell renal cell carcinoma (ccRCC). Here, the authors show that PBRM1 loss reduces IFNγ-mediated signalling resulting in a less immunogenic tumor microenvironment and that PBRM1 mutations correlate with lack of response to checkpoint inhibitor therapy in ccRCC patients..
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spelling doaj.art-2c2ffa7605cd4f008c5d3c780840e07f2022-12-21T22:59:33ZengNature PortfolioNature Communications2041-17232020-05-0111111410.1038/s41467-020-15959-6PBRM1 loss defines a nonimmunogenic tumor phenotype associated with checkpoint inhibitor resistance in renal carcinomaXian-De Liu0Wen Kong1Christine B. Peterson2Daniel J. McGrail3Anh Hoang4Xuesong Zhang5Truong Lam6Patrick G. Pilie7Haifeng Zhu8Kathryn E. Beckermann9Scott M. Haake10Sevinj Isgandrova11Margarita Martinez-Moczygemba12Nidhi Sahni13Nizar M. Tannir14Shiaw-Yih Lin15W. Kimryn Rathmell16Eric Jonasch17Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer CenterDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer CenterDepartment of Biostatistics, The University of Texas MD Anderson Cancer CenterDepartment of Systems Biology, The University of Texas MD Anderson Cancer CenterDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer CenterDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer CenterDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer CenterDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer CenterDepartment of Neuro-Oncology, The University of Texas MD Anderson Cancer CenterDivision of Hematology and Oncology, Vanderbilt University Medical CenterDivision of Hematology and Oncology, Vanderbilt University Medical CenterInstitute of Biosciences and Technology, Texas A&M Health Science CenterInstitute of Biosciences and Technology, Texas A&M Health Science CenterDepartment of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer CenterDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer CenterDepartment of Systems Biology, The University of Texas MD Anderson Cancer CenterVanderbilt-Ingram Cancer Center, Division of Hematology and Oncology, Department of Medicine, Vanderbilt University Medical CenterDepartment of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer CenterPBRM1, encoding for a subunit of the SWI/SNF complex, is the second most frequently mutated gene in clear cell renal cell carcinoma (ccRCC). Here, the authors show that PBRM1 loss reduces IFNγ-mediated signalling resulting in a less immunogenic tumor microenvironment and that PBRM1 mutations correlate with lack of response to checkpoint inhibitor therapy in ccRCC patients..https://doi.org/10.1038/s41467-020-15959-6
spellingShingle Xian-De Liu
Wen Kong
Christine B. Peterson
Daniel J. McGrail
Anh Hoang
Xuesong Zhang
Truong Lam
Patrick G. Pilie
Haifeng Zhu
Kathryn E. Beckermann
Scott M. Haake
Sevinj Isgandrova
Margarita Martinez-Moczygemba
Nidhi Sahni
Nizar M. Tannir
Shiaw-Yih Lin
W. Kimryn Rathmell
Eric Jonasch
PBRM1 loss defines a nonimmunogenic tumor phenotype associated with checkpoint inhibitor resistance in renal carcinoma
Nature Communications
title PBRM1 loss defines a nonimmunogenic tumor phenotype associated with checkpoint inhibitor resistance in renal carcinoma
title_full PBRM1 loss defines a nonimmunogenic tumor phenotype associated with checkpoint inhibitor resistance in renal carcinoma
title_fullStr PBRM1 loss defines a nonimmunogenic tumor phenotype associated with checkpoint inhibitor resistance in renal carcinoma
title_full_unstemmed PBRM1 loss defines a nonimmunogenic tumor phenotype associated with checkpoint inhibitor resistance in renal carcinoma
title_short PBRM1 loss defines a nonimmunogenic tumor phenotype associated with checkpoint inhibitor resistance in renal carcinoma
title_sort pbrm1 loss defines a nonimmunogenic tumor phenotype associated with checkpoint inhibitor resistance in renal carcinoma
url https://doi.org/10.1038/s41467-020-15959-6
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