4.6 Article

Association between SOD2 V16A variant and urological cancer risk

Journal

AGING-US
Volume 12, Issue 1, Pages 825-843

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/aging.102658

Keywords

SOD2; variant; urological cancer; in silico; analysis

Funding

  1. National Natural Science Foundation [81802576, 81902565]
  2. HighLevel Medical Talents Training Project [2016CZBJ035]
  3. Young Scientists Foundation of Changzhou No.2 People's Hospital [2019K008]
  4. Jiangsu Province Traditional Chinese Medicine Administration [YB201827]
  5. Wuxi Science and Technology Development Grant [CSE31N1605, WX18IIAN024]
  6. Jiangsu '333 Project' Scientific Research Grant [BRA 2016118]
  7. Wuxi City Medical Young Talent [QNRC043]
  8. Changzhou Sci and Tech program [CJ20190100]
  9. Changzhou 23rd Science and Technology Project [CZ20160017]
  10. Wuxi Commission of Health and Family Planning [J201803, Q201746, jzyx03, J201810, T201713, Z201712]
  11. Jiangsu Post-Doc Scientific Research Fund [1701184C]
  12. Wuxi Health and Family Planning Commission [ZM001]
  13. Jiangnan University Wuxi School of Medicine [1286010242190070]

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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.

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