Using gene and gene-set association tests to identify lethal prostate cancer genes.


Journal

Prostate cancer and prostatic diseases
ISSN: 1476-5608
Titre abrégé: Prostate Cancer Prostatic Dis
Pays: England
ID NLM: 9815755

Informations de publication

Date de publication:
17 Aug 2024
Historique:
received: 31 01 2024
accepted: 02 08 2024
revised: 26 07 2024
medline: 18 8 2024
pubmed: 18 8 2024
entrez: 17 8 2024
Statut: aheadofprint

Résumé

Recent advances in the detection and treatment of prostate cancer (PCa) have reduced morbidity and mortality from this common cancer. Despite these improvements, PCa remains the second leading cause of cancer death in men in the United States. Further understanding of the genetic underpinnings of lethal PCa is required to drive risk detection and prevention and ultimately reduce mortality. We therefore set out to identify germline variants associated with cases of lethal prostate cancer (LPCa). Using a two-stage study design, we compared whole-exome sequencing data of 550 LPCa patients to 488 healthy male controls. Men were classified as having LPCa based on medical record review. Candidate genes were identified using gene- and gene-set-based rare truncating variant association tests. Case-control burden testing through Firth's penalized logistic regression and case-gnomAD allelic burden testing through a one-sided mid-p Fisher's exact test were conducted. Each gene's p-values from these tests were combined into an omnibus p-value for candidate gene selection. In the subsequent validation stage, genes were assessed using the UK Biobank and Firth's penalized logistic regression for each ancestry, combined through meta-analysis. Gene-based rare variant association tests identified 12 genes nominally associated with LPCa. Rare-variant association tests identified a gene set with a significantly higher burden of truncating germline mutations in LPCa patients than controls. Combining gene- and gene-set test results, four nominally significant genes (PPP1R3A, TG, PPFIBP2, and BTN3A3) were selected as candidates. Subsequent validation using the UK Biobank found that PPP1R3A was significantly associated with LPCa risk (odds ratio 2.34, CI 1.20-4.59). Specifically, pGln662ArgfsTer7 was identified as the predominant variant in PPP1R3A among LPCa patients in our dataset. Both individual gene and gene-set analyses identified candidates associated with LPCa. The novel association of PPP1R3A and LPCa risk merits further investigation.

Sections du résumé

BACKGROUND BACKGROUND
Recent advances in the detection and treatment of prostate cancer (PCa) have reduced morbidity and mortality from this common cancer. Despite these improvements, PCa remains the second leading cause of cancer death in men in the United States. Further understanding of the genetic underpinnings of lethal PCa is required to drive risk detection and prevention and ultimately reduce mortality. We therefore set out to identify germline variants associated with cases of lethal prostate cancer (LPCa).
METHODS METHODS
Using a two-stage study design, we compared whole-exome sequencing data of 550 LPCa patients to 488 healthy male controls. Men were classified as having LPCa based on medical record review. Candidate genes were identified using gene- and gene-set-based rare truncating variant association tests. Case-control burden testing through Firth's penalized logistic regression and case-gnomAD allelic burden testing through a one-sided mid-p Fisher's exact test were conducted. Each gene's p-values from these tests were combined into an omnibus p-value for candidate gene selection. In the subsequent validation stage, genes were assessed using the UK Biobank and Firth's penalized logistic regression for each ancestry, combined through meta-analysis.
RESULTS RESULTS
Gene-based rare variant association tests identified 12 genes nominally associated with LPCa. Rare-variant association tests identified a gene set with a significantly higher burden of truncating germline mutations in LPCa patients than controls. Combining gene- and gene-set test results, four nominally significant genes (PPP1R3A, TG, PPFIBP2, and BTN3A3) were selected as candidates. Subsequent validation using the UK Biobank found that PPP1R3A was significantly associated with LPCa risk (odds ratio 2.34, CI 1.20-4.59). Specifically, pGln662ArgfsTer7 was identified as the predominant variant in PPP1R3A among LPCa patients in our dataset.
CONCLUSIONS CONCLUSIONS
Both individual gene and gene-set analyses identified candidates associated with LPCa. The novel association of PPP1R3A and LPCa risk merits further investigation.

Identifiants

pubmed: 39154125
doi: 10.1038/s41391-024-00879-z
pii: 10.1038/s41391-024-00879-z
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : U.S. Department of Defense (United States Department of Defense)
ID : PC150797
Organisme : U.S. Department of Health and Human Services (U.S. Department of Health & Human Services)
ID : 1S10OD021644-01A1

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

Bing-Jian Feng (BJ)

Department of Dermatology, University of Utah, Salt Lake City, UT, USA.

Julie L Boyle (JL)

Department of Family and Preventative Medicine, University of Utah, Salt Lake City, UT, USA.

Jun Wei (J)

Program for Personalized Cancer Care, NorthShore University HealthSystem, Evanston, Illinois, USA.

Courtney Carroll (C)

Department of Family and Preventative Medicine, University of Utah, Salt Lake City, UT, USA.

Nathan A Snyder (NA)

Department of Medicine and the Duke Cancer Institute, Duke University School of Medicine, Durham, NC, USA.

Zhuqing Shi (Z)

Program for Personalized Cancer Care, NorthShore University HealthSystem, Evanston, Illinois, USA.

S Lilly Zheng (SL)

Program for Personalized Cancer Care, NorthShore University HealthSystem, Evanston, Illinois, USA.

Jianfeng Xu (J)

Program for Personalized Cancer Care, NorthShore University HealthSystem, Evanston, Illinois, USA.

William B Isaacs (WB)

Department of Urology and the James Buchanan Brady Urologic Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Kathleen A Cooney (KA)

Department of Medicine and the Duke Cancer Institute, Duke University School of Medicine, Durham, NC, USA. kathleen.cooney@duke.edu.

Classifications MeSH