Purpose: Age-related factors including oxidative stress play an important role in prostate carcinogenesis. We hypothesize that germline single-nucleotide polymorphisms (SNPs) in oxidative stress pathway are associated with prostate cancer (PCa) risk. In this study, we aim to examine which of these SNPs is associated with PCa. Methods: Participants included in this analyses came from the “Genetic Susceptibility, Environment and Prostate Cancer Risk Study” conducted at the Veterans Affairs Portland Health Care System. After applying exclusion criteria, 231 PCa cases and 382 prostate biopsy-negative controls who had genotyping data on twenty-two single-nucleotide polymorphisms (SNPs) in six genes (MAPK14, NRF2, CAT, GPX1, GSTP1, SOD2, and XDH) associated with oxidative stress pathway were included in the analyses. The genotyping of SNPs was conducted by the Illumina BeadXpress VeraCode platform. We investigated these SNPs in relation to overall and aggressive PCa risk using logistic regression models controlling for relevant covariates. Results: One SNP in the MAPK14 (rs851023) was significantly associated with incident PCa risk. Compared to men carrying two copies of allele A, the presence of one or two copies of the G allele was associated with decreased risk of PCa [OR (95% CI) 0.19 (0.06–0.51)]. There was no statistically significant association between other SNPs in the NRF2, CAT, GPX1, GSTP1, SOD2, and XDH genes and PCa risk. Conclusions: The MAPK14 gene SNP rs851023 was associated with PCa and aggressive PCa risk after multiple comparison adjustment. Further studies in other populations or functional studies are needed to validate the finding.
|Number of pages||11|
|Journal||Cancer Causes and Control|
|State||Published - Dec 1 2019|
Bibliographical noteFunding Information:
We greatly appreciate all the veterans and their family members who contributed their time and effort to join the Genetic Susceptibility, Environment and Prostate Cancer Risk (GSEP) study. Gratitude is expressed to our large list of collaborators and providers of tools to make this project successful; use of Case Western University’s Genetic Risk Easy Assessment Tool (GREAT) was provided by Dr. Louise Acheson; Oregon Clinical and Translational Research Institute’s (OCTRI) Biomedical Informatics Program was instrumental in tying all of our electronic questionnaires together into one HIPAA-compliant portal; VAPHCS phlebotomy staff helped us collect research specimens and allowing laboratory space for saliva collection; OCTRI’s Clinical and Translational Research Center (CTRC) Core Laboratory processed, analyzed, and stored subjects’ biological specimens; genotyping was conducted by iGenix in Seattle, Washington. Dr. Shannon’s current and previous research coordinators spent large amounts of time with our numerous in-person and over-the-phone participants in support of this study, assuring quality data collection as well as close, personal attention to our nation’s veterans and their family members choosing to join this study. We are also grateful to VAPHCS Urology Nurses and Operative Care staff for supporting coordinators’ recruitment of research participants.
Research reported in this publication was supported by the Veterans Affairs’ Biomedical Laboratory Research and Development Merit Review Award, VA Portland Health Care System (VAPHCS), and by the National Center for Advancing Translational Sciences of the National Institutes of Health under award number UL1TR000128. Clinical Trial Registration’s clinicaltrials.gov identifier: NCT01013129. This work was directly supported by the Veterans Affairs’ Biomedical Laboratory Research and Development Merit Review Award, and Oregon Health & Science University/Oregon State University Cancer Prevention and Control Initiative (2017-Horizon-Knight-11). Acknowledgments
© 2019, Springer Nature Switzerland AG.
- Oxidative stress genes
- Prostate cancer
ASJC Scopus subject areas
- Cancer Research