Abstract

Background/aimA variation in the 3 prime untranslated regions (3′-UTRs) affects the binding of microRNA (miRNA) to the breast cancer (BC) susceptibility gene 1 (BRCA1) gene, and thus regulate its expression. In this study, the consequences of a variation in the miRNA-binding site (rs8176318G>T) in the 3′-UTRs of BRCA1 and its association with the risk of BC were investigated.Materials and methodsThe selected variation (rs8176318G>T) was genotyped in BC patients (n = 300) and healthy controls (n = 300) using allele-specific polymerase chain reaction (PCR) [tetra-primer amplification refractory mutation system-PCR (T-ARMS-PCR)]. The results of the T-ARMS-PCR were further confirmed by Sanger sequencing through a random selection of 10% previously analyzed samples by T-ARMS-PCR. Association of this variation with BC was tested by calculating the odds ratio (OR) (at 95% CI) and χ2-value using 4 different genetic models (codominant, dominant, recessive, and additive models).ResultsUsing Fisher’s exact test, a significant association between variant rs8176318 (G>T) and BC was found in codominant [χ2-value = 15.68, df: 2 P < 0.0004], dominant [OR = 1.557 (1.082–2.241), P <0.0213], recessive [OR = 0.474 (0.3204–0.7017), P = 0.0002] and additive models [OR = 1.609 (1.282–2.018), P < 0.0001].ConclusionIt was therefore concluded that there is a significant association between rs8176318 and BC risk in a case-control study in a Pakistani population. Furthermore, an association study using a large sample size is required to further verify these findings.

Highlights

  • Breast cancer (BC) is estimated to be the second leading cause of cancer related death in women worldwide [1]

  • Using Fisher’s exact test, a significant association between variant rs8176318 (G>T) and BC was found in codominant [χ2-value = 15.68, df: 2 P < 0.0004], dominant [odds ratio (OR) = 1.557 (1.082–2.241), P

  • It was concluded that there is a significant association between rs8176318 and BC risk in a case-control study in a Pakistani population

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Summary

Introduction

Breast cancer (BC) is estimated to be the second leading cause of cancer related death in women worldwide [1]. There are several environmental and genetic factors contributing to BC. A number of protein coding and noncoding genes contribute to the etiology of BC. BC susceptibility gene 1 (BRCA 1) is one of the main protein-coding genes related to the causes of BC. Mutations in BRCA1 account for about 40%–45% of BCs [2]. BRCA1 is involved in repairing breaks in double-stranded DNA, transcription, and recombination. The frequency and types of mutations in BRCA1 vary among different populations worldwide. The 3 prime untranslated regions (3′-UTRs) of BRCA1 play a pivotal role in the stability, localization, and transport

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