Literature DB >> 24365257

SRD5A2 gene polymorphisms affect the risk of breast cancer.

Amirtharaj Francis1, Saumya Sarkar2, Singh Pooja3, Daminani Surekha4, Digumarthi Raghunatha Rao5, Lakshmi Rao6, Lingadakai Ramachandra7, Satti Vishnupriya4, Kapaettu Satyamoorthy8, Kumarasamy Thangaraj9, Singh Rajender10.   

Abstract

Androgens in breast cancer have been studied alone and in correlation with estrogens as estrogen to testosterone ratio. 5-α-reductase is one of the important enzymes participating in androgen metabolism, which affects androgen activity by affecting conversion of testosterone to dihydrotestosterone. We hypothesized that polymorphisms in the SRD5A2 gene (encoding 5-α-reductase) may affect breast cancer risk by affecting total androgen activity. Complete coding region of the SRD5A2 gene was sequenced in a group of 628 patients and 244 control samples from three southern states (Tamil Nadu, Andhra Pradesh, and Karnataka) of India. We observed three common polymorphisms in this gene; namely, A49T, V89L, and (TA)n repeats. A49T locus was monomorphic in the study population, but V89L showed a strong correlation with breast cancer (P = 0.03, OR = 1.40, CI = 1.02-1.91). (TA)0/(TA)9 and (TA)9/(TA)9 genotypes were at a lower risk of breast cancer (P = 0.01, OR = 0.64, CI = 0.46-0.90). We conclude that SRD5A2 genotypes significantly affect breast cancer risk in the South Indian populations.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Breast cancer; Polymorphism; SRD5A2 gene

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Year:  2013        PMID: 24365257     DOI: 10.1016/j.breast.2013.11.010

Source DB:  PubMed          Journal:  Breast        ISSN: 0960-9776            Impact factor:   4.380


  3 in total

Review 1.  Integrative and Analytical Review of the 5-Alpha-Reductase Type 2 Deficiency Worldwide.

Authors:  Rafael Loch Batista; Berenice Bilharinho Mendonca
Journal:  Appl Clin Genet       Date:  2020-04-14

2.  Role of CD5L and SRD5A2 as Prognostic Biomarkers for Hepatocellular Carcinoma.

Authors:  Yunxiu Luo; Xiaopeng Huang; Jiabin Zhan; Shuai Zhang
Journal:  Int J Gen Med       Date:  2021-12-01

3.  Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency.

Authors:  Erdal Eren; Tuba Edgünlü; Emre Asut; Sevim Karakaş Çelik
Journal:  J Clin Res Pediatr Endocrinol       Date:  2016-01-12
  3 in total

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