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PBRM1 Inactivation Promotes Upregulation of Human Endogenous Retroviruses in a HIF-Dependent Manner

Clear cell renal cell carcinoma (ccRCC) is considered an immunotherapy-responsive disease; however, the reasons for this remain unclear. Studies have variably implicated PBRM1 mutations as a predictive biomarker of immune checkpoint blockade (ICB) response, and separate studies demonstrate that expr...

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Autores principales: Zhou, Mi, Leung, Janet Y., Gessner, Kathryn H., Hepperla, Austin J., Simon, Jeremy M., Davis, Ian J., Kim, William Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for Cancer Research 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898299/
https://www.ncbi.nlm.nih.gov/pubmed/35013001
http://dx.doi.org/10.1158/2326-6066.CIR-21-0480
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author Zhou, Mi
Leung, Janet Y.
Gessner, Kathryn H.
Hepperla, Austin J.
Simon, Jeremy M.
Davis, Ian J.
Kim, William Y.
author_facet Zhou, Mi
Leung, Janet Y.
Gessner, Kathryn H.
Hepperla, Austin J.
Simon, Jeremy M.
Davis, Ian J.
Kim, William Y.
author_sort Zhou, Mi
collection PubMed
description Clear cell renal cell carcinoma (ccRCC) is considered an immunotherapy-responsive disease; however, the reasons for this remain unclear. Studies have variably implicated PBRM1 mutations as a predictive biomarker of immune checkpoint blockade (ICB) response, and separate studies demonstrate that expression of human endogenous retroviruses (hERV) might be an important class of tumor-associated antigens. We sought to understand whether specific mutations were associated with hERV expression. Two large, annotated genomic datasets, TCGA KIRC and IMmotion150, were used to correlate mutations and hERV expression. PBRM1 mutations were consistently associated with increased hERV expression in primary tumors. In vitro silencing of PBRM1, HIF1A, and HIF2A followed by RNA sequencing was performed in UMRC2 cells, confirming that PBRM1 regulates hERVs in a HIF1α- and HIF2α-dependent manner and that hERVs of the HERVERI superfamily are enriched in PBRM1-regulated hERVs. Our results uncover a role for PBRM1 in the negative regulation of hERVs in ccRCC. Moreover, the HIF-dependent nature of hERV expression explains the previously reported ccRCC-specific clinical associations of PBRM1-mutant ccRCC with both a good prognosis as well as improved clinical outcomes to ICB. See related Spotlight by Labaki et al., p. 274.
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spelling pubmed-88982992022-03-06 PBRM1 Inactivation Promotes Upregulation of Human Endogenous Retroviruses in a HIF-Dependent Manner Zhou, Mi Leung, Janet Y. Gessner, Kathryn H. Hepperla, Austin J. Simon, Jeremy M. Davis, Ian J. Kim, William Y. Cancer Immunol Res Priority Brief Clear cell renal cell carcinoma (ccRCC) is considered an immunotherapy-responsive disease; however, the reasons for this remain unclear. Studies have variably implicated PBRM1 mutations as a predictive biomarker of immune checkpoint blockade (ICB) response, and separate studies demonstrate that expression of human endogenous retroviruses (hERV) might be an important class of tumor-associated antigens. We sought to understand whether specific mutations were associated with hERV expression. Two large, annotated genomic datasets, TCGA KIRC and IMmotion150, were used to correlate mutations and hERV expression. PBRM1 mutations were consistently associated with increased hERV expression in primary tumors. In vitro silencing of PBRM1, HIF1A, and HIF2A followed by RNA sequencing was performed in UMRC2 cells, confirming that PBRM1 regulates hERVs in a HIF1α- and HIF2α-dependent manner and that hERVs of the HERVERI superfamily are enriched in PBRM1-regulated hERVs. Our results uncover a role for PBRM1 in the negative regulation of hERVs in ccRCC. Moreover, the HIF-dependent nature of hERV expression explains the previously reported ccRCC-specific clinical associations of PBRM1-mutant ccRCC with both a good prognosis as well as improved clinical outcomes to ICB. See related Spotlight by Labaki et al., p. 274. American Association for Cancer Research 2022-03-01 2022-03-03 /pmc/articles/PMC8898299/ /pubmed/35013001 http://dx.doi.org/10.1158/2326-6066.CIR-21-0480 Text en ©2022 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license.
spellingShingle Priority Brief
Zhou, Mi
Leung, Janet Y.
Gessner, Kathryn H.
Hepperla, Austin J.
Simon, Jeremy M.
Davis, Ian J.
Kim, William Y.
PBRM1 Inactivation Promotes Upregulation of Human Endogenous Retroviruses in a HIF-Dependent Manner
title PBRM1 Inactivation Promotes Upregulation of Human Endogenous Retroviruses in a HIF-Dependent Manner
title_full PBRM1 Inactivation Promotes Upregulation of Human Endogenous Retroviruses in a HIF-Dependent Manner
title_fullStr PBRM1 Inactivation Promotes Upregulation of Human Endogenous Retroviruses in a HIF-Dependent Manner
title_full_unstemmed PBRM1 Inactivation Promotes Upregulation of Human Endogenous Retroviruses in a HIF-Dependent Manner
title_short PBRM1 Inactivation Promotes Upregulation of Human Endogenous Retroviruses in a HIF-Dependent Manner
title_sort pbrm1 inactivation promotes upregulation of human endogenous retroviruses in a hif-dependent manner
topic Priority Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898299/
https://www.ncbi.nlm.nih.gov/pubmed/35013001
http://dx.doi.org/10.1158/2326-6066.CIR-21-0480
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