SRD5A2 gene polymorphisms and the risk of benign prostatic hyperplasia but not prostate cancer

Choubey, Vimal Kumar ; Sankhwar, Satya Narayan ; Carlus, S. Justin ; Singh, Anand Narayan ; Dalela, Divakar ; Thangaraj, Kumarasamy ; Rajender, Singh (2015) SRD5A2 gene polymorphisms and the risk of benign prostatic hyperplasia but not prostate cancer Asian Pacific Journal of Cancer Prevention, 16 (3). pp. 1033-1036. ISSN 1513-7368

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Background: Testosterone, a primary androgen in males, is converted into its most active form,Dihydrotestosterone (DHT), by 5α-reductase type 2 (encoded by the SRD5A2 gene) in the prostate. DHT is necessary for prostatic growth and has five times higher binding affinity than testosterone for androgen receptors. We hypothesized that polymorphic variations in the SRD5A2 gene may affect the risk of benign prostatichyperplasia and prostate cancer. Materials and Methods: We analyzed SRD5A2 gene polymorphisms in 217 BPH patients, 192 PCa cases and 171 controls. Genotyping was undertaken using direct DNA sequencing. Genotype data were compared between cases and controls using a Chi square statistical tool. Results: We found that the A49T locus was monomorphic with ‘AA’ genotype in all subjects. At V89L locus, the presence of ‘VV’ showed a marginally significant correlation with increased BPH risk (p = 0.047). At the (TA)n locus, longer TA repeats were found to be protective against BPH (p = 0.003). However, neither of these polymoprhisms correlated with the risk of PCa. Conclusions: We conclude that A49T is monomorphic in the study population, VV marginally correlates with BPH risk and longer (TA) n repeats are protective against BPH. None of these polymorphisms affect the risk of PCa.

Item Type:Article
Source:Copyright of this article belongs to Asian Pacific Education Press Ltd.
Keywords:5α-Reductase Type 2; Benign Prostatic Hyperplasia; Genetic Polymorphism; Prostate Cancer; SRD5A2
ID Code:107751
Deposited On:21 Jul 2017 12:01
Last Modified:21 Jul 2017 12:01

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