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Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

Authors :
Mitchell J
Camacho N
Shea P
Stopsack KH
Joseph V
Burren O
Dhindsa R
Nag A
Berchuck JE
O'Neill A
Abbasi A
Zoghbi AW
Alegre-Díaz J
Kuri-Morales P
Berumen J
Tapia-Conyer R
Emberson J
Torres JM
Collins R
Wang Q
Goldstein D
Matakidou A
Haefliger C
Anderson-Dring L
March R
Jobanputra V
Dougherty B
Carss K
Petrovski S
Kantoff PW
Offit K
Mucci LA
Pomerantz M
Fabre MA
Source :
MedRxiv : the preprint server for health sciences [medRxiv] 2024 May 10. Date of Electronic Publication: 2024 May 10.
Publication Year :
2024

Abstract

The etiology of prostate cancer, the second most common cancer in men globally, has a strong heritable component. While rare coding germline variants in several genes have been identified as risk factors from candidate gene and linkage studies, the exome-wide spectrum of causal rare variants remains to be fully explored. To more comprehensively address their contribution, we analysed data from 37,184 prostate cancer cases and 331,329 male controls from five cohorts with germline exome/genome sequencing and one cohort with imputed array data from a population enriched in low-frequency deleterious variants. Our gene-level collapsing analysis revealed that rare damaging variants in SAMHD1 as well as genes in the DNA damage response pathway ( BRCA2 , ATM and CHEK2 ) are associated with the risk of overall prostate cancer. We also found that rare damaging variants in AOX1 and BRCA2 were associated with increased severity of prostate cancer in a case-only analysis of aggressive versus non-aggressive prostate cancer. At the single-variant level, we found rare non-synonymous variants in three genes ( HOXB13 , CHEK2 , BIK ) significantly associated with increased risk of overall prostate cancer and in four genes ( ANO7 , SPDL1 , AR , TERT ) with decreased risk. Altogether, this study provides deeper insights into the genetic architecture and biological basis of prostate cancer risk and severity.<br />Competing Interests: Competing Interests J.M., N.C., O.B., R.D., A.N., A.O., A.A., Q.W., L.A.-D., R.M., B.D., K.C., S.P., M.A.F. are current employees and/or stockholders of AstraZeneca. A.W.Z receives grant funding and consulting fees from AstraZeneca. L.A.M. is on the advisory board and holds equity interest in Convergent Therapeutics. A.M. is a former employee of AstraZeneca and current employee of GSK and a stockholder of AstraZeneca and GSK. C.H. was an employee and stockholder of AZ at the time of study. P.W.K. is a co-founder and employee of Convergent Therapeutics.

Details

Language :
English
Database :
MEDLINE
Journal :
MedRxiv : the preprint server for health sciences
Accession number :
38766261
Full Text :
https://doi.org/10.1101/2024.05.10.24307164