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作 者:付莉[1] 陈双龙[1] 黄红浪[1] 骆伟珍[1] 范钦[2]
机构地区:[1]厦门大学附属第一医院,福建厦门361003 [2]南方医科大学中医药学院
出 处:《山东医药》2013年第15期4-6,共3页Shandong Medical Journal
基 金:国家自然科学基金资助项目(81173616);福建省卫生厅青年科研课题(2009-2-78)
摘 要:目的探讨成纤维细胞生长因子受体2(FGFR2)基因rs2981582位点单核苷酸多态性(SNP)与乳腺癌易感性之间的关系。方法对193例乳腺癌患者和150例正常女性进行病例对照研究,采用DNA直接测序法同时检测其FGFR2基因第二内含子的SNP位点rs2981582的基因及基因型。结果乳腺癌患者FGFR2基因rs2981582位点的基因分布频率与正常女性相比,P>0.05;对该位点的基因分布频率与乳腺癌雌激素受体(ER)表达状态进行分析后发现,等位基因T的频率在ER阳性乳腺癌患者中为43.93%,在正常女性中为34.67%,两者相比,P<0.05(OR为1.476)。结论 FGFR2基因第2内含子rs2981582位点的SNP与ER阳性乳腺癌的发生显著相关,携带等位基因T的个体患病风险增加。Objective To study the relationship between single nucleotide polymorphism (SNP) of fibroblast growth factor receptors 2 ( FGFR2, rs2981582 ) and the susceptibility of breast cancer in Chinese women. Methods Case-con- trol study was performed in 193 histological confirmed breast cancer eases and 150 cases of normal women as controls. rs2981582 of FGFR2 gene mad its genetype were determined by PCR-direet sequencing. Results There were no significant differences in the allele frequencies of rs2981582 C/T of FGFR2 gene between cases and controls (P 〉 0.05 ). The gene frequency distribution and the expression of estrogen receptor (ER) in breast cancer were further analyzed. The minor al- lele T frequency of rs2981582 was 43.93% of cases whereas 34.67% of controls, the allele frequencies in the cases were significantly different from those of the controls ( P 〈 0.05 ), the odds ratio ( OR = 1. 476 ) also showed a higher risk of breast cancer in individuals carrying the minor alleles. Conclusion The FGFR2 polymorphism rs2981582 C/T may con- tribute to the susceptibility of breast cancer with ER positive in Chinese women.
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