Associations Between Polymorphisms in Genes Related to Oxidative Stress and DNA Repair, Interactions With Serum Antioxidants, and Prostate Cancer Risk: Results From the Prostate Cancer Prevention Trial.

DNA repair genetic polymorphisms oxidative stress prostate cancer serum antioxidant

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2021
Historique:
received: 03 11 2021
accepted: 21 12 2021
entrez: 31 1 2022
pubmed: 1 2 2022
medline: 1 2 2022
Statut: epublish

Résumé

Study of polymorphisms in genes related to the generation and removal of oxidative stress and repair of oxidative DNA damage will lead to new insights into the genetic basis of prostate cancer. In the Prostate Cancer Prevention Trial (PCPT), a double-blind, randomized controlled trial testing finasteride versus placebo for prostate cancer prevention, we intend to investigate the role of oxidative stress/DNA repair mechanisms in prostate cancer etiology and whether these polymorphisms modify prostate cancer risk by interacting with antioxidant status in both placebo and finasteride arms. We evaluated associations of selected candidate polymorphisms in genes in these pathways, and interactions with pre-diagnostic serum antioxidants, and the risk of prostate cancer among 1,598 cases and 1,706 frequency-matched controls enrolled in the PCPT. Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated using multivariable-adjusted logistic regression models. While there were no statistically significant associations observed in the placebo arm, several SNPs were associated with prostate cancer in the finasteride arm. Specifically,

Identifiants

pubmed: 35096612
doi: 10.3389/fonc.2021.808715
pmc: PMC8795906
doi:

Types de publication

Journal Article

Langues

eng

Pagination

808715

Subventions

Organisme : NCI NIH HHS
ID : U01 CA182883
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189974
Pays : United States
Organisme : NCI NIH HHS
ID : UM1 CA182883
Pays : United States

Informations de copyright

Copyright © 2022 Gong, Platek, Till, Goodman, Tangen, Platz, Neuhouser, Thompson, Santella and Ambrosone.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Zhihong Gong (Z)

Department of Cancer Prevention & Control, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.

Mary E Platek (ME)

Department of Cancer Prevention & Control, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.

Cathee Till (C)

Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, United States.

Phyllis J Goodman (PJ)

Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, United States.

Catherine M Tangen (CM)

Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, United States.

Elizabeth A Platz (EA)

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, MD, United States.

Marian L Neuhouser (ML)

Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, United States.

Ian M Thompson (IM)

Department of Urology, University of Texas Health Science Center, San Antonio, TX, United States.

Regina M Santella (RM)

Department of Environmental Health Sciences and Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY, United States.

Christine B Ambrosone (CB)

Department of Cancer Prevention & Control, Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.

Classifications MeSH