Romanowicz-Makowska Hanna, Sobczuk Anna, Smolarz Beata, Fiks Tomasz, Kulig Andrzej
Laboratory of Molecular Genetics, Department of Pathology, Institute of Polish Mother's Memorial Hospital, Lódź.
Pol J Pathol. 2007;58(4):245-9.
Common polymorphism in DNA repair genes may alter protein function and an individual's capacity to repair damaged DNA; deficits in repair capacity may lead to genetic instability and carcinogenesis. In present work we investigated the association between XPD Lys751Gln polymorphism and breast cancer progression. The polymorphism was analysed in breast cancer patients (n = 92) in blood. Blood samples from age matched healthy women served as control (n = 110). XPD genotypes were measured by PCR-RFLP. The distribution of the genotypes of the Lys751Gln polymorphism in patients differed significantly (p < 0.05) from those predicted by the Hardy-Weinberg equilibrium. There were significant differences in the frequencies of alleles between the breast cancer subjects and controls (p < 0.05). The results support the hypothesis that the Lys751Gln polymorphism of XPD gene may be associated with the incidence of breast cancer.
DNA修复基因中的常见多态性可能会改变蛋白质功能以及个体修复受损DNA的能力;修复能力的缺陷可能导致基因不稳定和致癌作用。在本研究中,我们调查了XPD Lys751Gln多态性与乳腺癌进展之间的关联。对92例乳腺癌患者的血液样本进行了该多态性分析。年龄匹配的健康女性的血液样本作为对照(n = 110)。通过PCR-RFLP测定XPD基因型。患者中Lys751Gln多态性的基因型分布与哈迪-温伯格平衡预测的分布有显著差异(p < 0.05)。乳腺癌患者和对照组之间的等位基因频率存在显著差异(p < 0.05)。结果支持以下假设:XPD基因的Lys751Gln多态性可能与乳腺癌的发病率有关。