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Association between SOD2 V16A variant and urological cancer risk
Background: The correlation between superoxide dismutase 2 (SOD2) V16A variant and urological cancer susceptibility has been widely studied, however, with divergent results. Results: Totally, 9,910 cancer patients and 11,239 control subjects were enrolled. V16A variant is associated with an increase...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977677/ https://www.ncbi.nlm.nih.gov/pubmed/31929112 http://dx.doi.org/10.18632/aging.102658 |
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author | Zhang, Li-Feng Xu, Kai Tang, Bo-Wen Zhang, Wei Yuan, Wei Yue, Chuang Shi, Li Mi, Yuan-Yuan Zuo, Li Zhu, Li-Jie |
author_facet | Zhang, Li-Feng Xu, Kai Tang, Bo-Wen Zhang, Wei Yuan, Wei Yue, Chuang Shi, Li Mi, Yuan-Yuan Zuo, Li Zhu, Li-Jie |
author_sort | Zhang, Li-Feng |
collection | PubMed |
description | Background: The correlation between superoxide dismutase 2 (SOD2) V16A variant and urological cancer susceptibility has been widely studied, however, with divergent results. Results: Totally, 9,910 cancer patients and 11,239 control subjects were enrolled. V16A variant is associated with an increased susceptibility to urological cancer (A-allele vs. V-allele: OR = 1.06, 95% CI = 1.00 – 1.13, P = 0.047; AA+AV vs. VV: OR = 1.09, 95% CI = 1.02 – 1.16, P = 0.008), especially for prostate cancer (PCa). Serum SOD2 level of PCa patients with VV+VA genotypes was lower than in those with AA genotypes. SOD2 expression is downregulated in both prostate and bladder cancer, as compared to the control. Furthermore, SOD2 was found to be downregulated in more advanced PCa participants, as compared to the ones in early stages. PCa subjects with low SOD2 expression displayed a shorter disease-free survival (DFS) time compared to that of the high SOD2 expression counterparts. Conclusions: The SOD2 V16A variant may be associated with increased urological cancer susceptibility, especially for prostate cancer. Methods: A pooled analysis utilizing odds ratios (ORs), in silico tools and ELISA was adopted to demonstrate this association. We also used immunohistochemical staining (IHS) to assess SOD2 expression. |
format | Online Article Text |
id | pubmed-6977677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-69776772020-01-31 Association between SOD2 V16A variant and urological cancer risk Zhang, Li-Feng Xu, Kai Tang, Bo-Wen Zhang, Wei Yuan, Wei Yue, Chuang Shi, Li Mi, Yuan-Yuan Zuo, Li Zhu, Li-Jie Aging (Albany NY) Research Paper Background: The correlation between superoxide dismutase 2 (SOD2) V16A variant and urological cancer susceptibility has been widely studied, however, with divergent results. Results: Totally, 9,910 cancer patients and 11,239 control subjects were enrolled. V16A variant is associated with an increased susceptibility to urological cancer (A-allele vs. V-allele: OR = 1.06, 95% CI = 1.00 – 1.13, P = 0.047; AA+AV vs. VV: OR = 1.09, 95% CI = 1.02 – 1.16, P = 0.008), especially for prostate cancer (PCa). Serum SOD2 level of PCa patients with VV+VA genotypes was lower than in those with AA genotypes. SOD2 expression is downregulated in both prostate and bladder cancer, as compared to the control. Furthermore, SOD2 was found to be downregulated in more advanced PCa participants, as compared to the ones in early stages. PCa subjects with low SOD2 expression displayed a shorter disease-free survival (DFS) time compared to that of the high SOD2 expression counterparts. Conclusions: The SOD2 V16A variant may be associated with increased urological cancer susceptibility, especially for prostate cancer. Methods: A pooled analysis utilizing odds ratios (ORs), in silico tools and ELISA was adopted to demonstrate this association. We also used immunohistochemical staining (IHS) to assess SOD2 expression. Impact Journals 2020-01-12 /pmc/articles/PMC6977677/ /pubmed/31929112 http://dx.doi.org/10.18632/aging.102658 Text en Copyright © 2020 Zhang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Zhang, Li-Feng Xu, Kai Tang, Bo-Wen Zhang, Wei Yuan, Wei Yue, Chuang Shi, Li Mi, Yuan-Yuan Zuo, Li Zhu, Li-Jie Association between SOD2 V16A variant and urological cancer risk |
title | Association between SOD2 V16A variant and urological cancer risk |
title_full | Association between SOD2 V16A variant and urological cancer risk |
title_fullStr | Association between SOD2 V16A variant and urological cancer risk |
title_full_unstemmed | Association between SOD2 V16A variant and urological cancer risk |
title_short | Association between SOD2 V16A variant and urological cancer risk |
title_sort | association between sod2 v16a variant and urological cancer risk |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977677/ https://www.ncbi.nlm.nih.gov/pubmed/31929112 http://dx.doi.org/10.18632/aging.102658 |
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