Investigation of the 1758G > C and 2880A > G variants within the NCOA3 gene in a breast cancer affected Australian population

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Title Investigation of the 1758G > C and 2880A > G variants within the NCOA3 gene in a breast cancer affected Australian population
Author Gabrovska, Pam; Smith, Robert Anthony; O'Leary, Greg; Haupt, Larisa; Griffiths, Lyn
Journal Name Gene
Year Published 2011
Place of publication Netherlands
Publisher Elsevier
Abstract NCOA3 is a known low to moderate-risk breast cancer susceptibility gene, amplified in 5–10% and over expressed in about 60% of breast tumours. Additionally, this over expression is associated with Tamoxifen resistance and poor prognosis. Previously, two variants of NCOA3, 1758G > C and 2880A > G have been associated with breast cancer in two independent populations. Here we assessed the influence of the two NCOA3 variants on breast cancer risk by genotyping an Australian case–control study population. 172 cases and 178 controls were successfully genotyped for the 1758G > C variant and 186 cases and 182 controls were successfully genotyped for the 2880A > G variant using high-resolution melt analysis (HRM). The genotypes of the 1758G > C variant were validated by sequencing. χ2 tests were performed to determine if significant differences exist in the genotype and allele frequencies between the cases and controls. χ2 analysis returned no statistically significant difference (p > 0.05) for genotype frequencies between cases and controls for 1758G > C (χ2 = 0.97, p = 0.6158) or 2880A > G (χ2 = 2.09, p = 0.3516). Similarly, no statistical difference was observed for allele frequencies for 1758G > C (χ2 = 0.07, p = 0.7867) or 2880A > G (χ2 = 0.04, p = 0.8365). Haplotype analysis of the two SNPs also showed no difference between the cases and the controls (p = 0.9585). Our findings in an Australian Caucasian population composed of breast cancer sufferers and an age matched control population did not support the findings of previous studies demonstrating that these markers play a significant role in breast cancer susceptibility. Here, no significant difference was detected between breast cancer patients and healthy matched controls by either the genotype or allele frequencies for the investigated variants (all p ≥ 0.05). While an association of the two variants and breast cancer was not detected in our case–control study population, exploring these variants in a larger population of the same kind may obtain results in concordance with previous studies. Given the importance of NCOA3 and its involvement in biological processes involved in breast cancer and the possible implications variants of the gene could have on the response to Tamoxifen therapy, NCOA3 remains a candidate for further investigations.
Peer Reviewed Yes
Published Yes
Alternative URI http://dx.doi.org/10.1016/j.gene.2011.05.001
Volume 482
Issue Number 1-2
Page from 68
Page to 72
ISSN 0378-1119
Date Accessioned 2012-03-08; 2012-03-21T23:05:57Z
Date Available 2012-03-21T23:05:57Z
Research Centre Griffith Health Institute; Molecular Basis of Disease
Faculty Griffith Health Faculty
Subject Genome Structure and Regulation
URI http://hdl.handle.net/10072/43757
Publication Type Journal Articles (Refereed Article)
Publication Type Code c1

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