Open AccessDNA repair gene XRCC3 241Met variant and breast cancer susceptibility of Azeri population in Iranian
Author(s) -
Sahar Gohari-Lasaki,
Jalal Gharesouran,
Morteza Ghojazadeh,
Vahid Montazeri,
Hakimeh Saadatian,
Seyyed Ardebili Mojtaba
Publication year - 2015
Publication title -
genetika
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.24
H-Index - 15
eISSN - 1820-6069
pISSN - 0534-0012
DOI - 10.2298/gensr1502733g
Subject(s) - xrcc3 , breast cancer , genotype , dna repair , rad51 , genetics , allele , biology , population , homologous recombination , oncology , gene , cancer research , cancer , medicine , single nucleotide polymorphism , environmental health
DNA-repair systems are essential for repairing damage that occurs when there is recombination between homologous chromosomes. The gene XRCC3 (X-ray cross complementing group 3) encodes a member of the RecA/Rad51-related protein family that participates in homologous recombination to maintain chromosome stability and repair DNA damage. The Thr241Met XRCC3-18067C>T, rs861539) substitution, a C to T transition at codon 241 in exon7, thus plays critical roles in cancer development. The aim of this study was association between XRCC3 Thr241Met polymorphism and risk of sporadic breast cancer in Azari population. We analysed DNA samples from 100 sporadic breast cancer patients and 100 healthy women, for XRCC3 Thr241Met polymorphism using PCR-RFLP. Genotype specific risks were tested using chi-test with 95% confident intervals. Frequency of Thr/Thr at codon 241was 69% in controls and 70% in patients, Thr/Met frequency was 22% in controls and 13 % in patients, the Met/Met genotype was 9% incontrols and 17% in patients. No correlation between the genotype and allele distribution and increased susceptibility for breast Cancer. Our results suggested that in pre-menopausal women, breast cancer riskis not significantly associated with rs861539 in Azari population