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成纤维细胞生长因子受体 2(FGFR2)的遗传变异与汉族中国女性的乳腺癌风险相关。

Genetic variants of fibroblast growth factor receptor 2 (FGFR2) are associated with breast cancer risk in Chinese women of the Han nationality.

机构信息

Life Sciences School of Hubei University, 368 Youyi Road, Wuchang, Wuhan 430062, China.

出版信息

Immunogenetics. 2012 Jan;64(1):71-6. doi: 10.1007/s00251-011-0564-2. Epub 2011 Aug 6.

DOI:10.1007/s00251-011-0564-2
PMID:21822685
Abstract

Fibroblast growth factor receptor 2 (FGFR2), a recently described risk factor for breast cancer, plays important roles in cell growth, invasiveness, motility, and angiogenesis. In attempt to investigate whether FGFR2 polymorphisms are associated with a risk of breast cancer in Chinese women of the Han nationality, we genotyped single-nucleotide polymorphisms (SNPs) of seven FGFR2 sites (rs2981582, rs17102287, rs17542768, rs10510097, rs11200012, rs3750817, rs2981578) in 816 women including 388 breast cancer patients and 428 healthy controls via the polymerase chain reaction single-strand conformation polymorphism procedure as well as sequence detection. Our results suggest that the A allele and AA genotype of SNP rs2981578 appear to be protective factors associated with breast cancer, while the CT genotype of SNP rs3750817 is a putative risk factor.

摘要

成纤维细胞生长因子受体 2(FGFR2)是最近被描述的乳腺癌风险因素,在细胞生长、侵袭性、运动性和血管生成中发挥重要作用。为了探讨 FGFR2 多态性是否与汉族中国女性乳腺癌的风险相关,我们通过聚合酶链反应单链构象多态性程序以及序列检测,对包括 388 例乳腺癌患者和 428 例健康对照在内的 816 名女性的 7 个 FGFR2 位点(rs2981582、rs17102287、rs17542768、rs10510097、rs11200012、rs3750817、rs2981578)的单核苷酸多态性(SNP)进行了基因分型。我们的结果表明,SNP rs2981578 的 A 等位基因和 AA 基因型似乎是与乳腺癌相关的保护因素,而 SNP rs3750817 的 CT 基因型则是一个可能的风险因素。

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2
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本文引用的文献

1
Variation in the FGFR2 gene and the effects of postmenopausal hormone therapy on invasive breast cancer.FGFR2 基因的变异与绝经后激素治疗对浸润性乳腺癌的影响。
Cancer Epidemiol Biomarkers Prev. 2009 Nov;18(11):3079-85. doi: 10.1158/1055-9965.EPI-09-0611. Epub 2009 Oct 27.
2
FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation.FGFR2基因变异与乳腺癌风险:利用非裔美国人研究进行精细定位及染色质构象分析
Hum Mol Genet. 2009 May 1;18(9):1692-703. doi: 10.1093/hmg/ddp078. Epub 2009 Feb 17.
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Genetic variants in fibroblast growth factor receptor 2 (FGFR2) contribute to susceptibility of breast cancer in Chinese women.
Functional Screenings Identify Regulatory Variants Associated with Breast Cancer Susceptibility.
功能筛选鉴定与乳腺癌易感性相关的调控变异。
Curr Issues Mol Biol. 2021 Oct 26;43(3):1756-1777. doi: 10.3390/cimb43030124.
4
Copy number alternations of the 17q23-rs6504950 locus are associated with advanced breast cancers in Taiwanese women.17q23-rs6504950位点的拷贝数改变与台湾女性的晚期乳腺癌相关。
Tzu Chi Med J. 2019 Jun 17;32(2):193-197. doi: 10.4103/tcmj.tcmj_45_19. eCollection 2020 Apr-Jun.
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Fibroblast Growth Factor Receptor 2 Signaling in Breast Cancer.成纤维细胞生长因子受体 2 在乳腺癌中的信号转导。
Int J Biol Sci. 2017 Sep 5;13(9):1163-1171. doi: 10.7150/ijbs.20792. eCollection 2017.
6
Association between FGFR2 (rs2981582, rs2420946 and rs2981578) polymorphism and breast cancer susceptibility: a meta-analysis.FGFR2基因(rs2981582、rs2420946和rs2981578)多态性与乳腺癌易感性的关联:一项荟萃分析。
Oncotarget. 2017 Jan 10;8(2):3454-3470. doi: 10.18632/oncotarget.13839.
7
TNRC9 rs12443621 and FGFR2 rs2981582 polymorphisms and breast cancer risk.TNRC9基因rs12443621位点和FGFR2基因rs2981582位点多态性与乳腺癌风险
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8
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Biomed Res Int. 2015;2015:626948. doi: 10.1155/2015/626948. Epub 2015 Sep 3.
9
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10
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Breast Cancer Res Treat. 2013 Aug;140(3):587-601. doi: 10.1007/s10549-013-2644-5. Epub 2013 Aug 3.
成纤维细胞生长因子受体2(FGFR2)中的基因变异会增加中国女性患乳腺癌的易感性。
Carcinogenesis. 2008 Dec;29(12):2341-6. doi: 10.1093/carcin/bgn235. Epub 2008 Oct 8.
4
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Allele-specific up-regulation of FGFR2 increases susceptibility to breast cancer.FGFR2的等位基因特异性上调增加了患乳腺癌的易感性。
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Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.全基因组关联研究为位于6q22.33的一个乳腺癌风险基因座提供了证据。
Proc Natl Acad Sci U S A. 2008 Mar 18;105(11):4340-5. doi: 10.1073/pnas.0800441105. Epub 2008 Mar 7.
8
Clinical correlates of low-risk variants in FGFR2, TNRC9, MAP3K1, LSP1 and 8q24 in a Dutch cohort of incident breast cancer cases.荷兰新发乳腺癌病例队列中FGFR2、TNRC9、MAP3K1、LSP1和8q24低风险变异的临床关联
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A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.一项全基因组关联研究确定了FGFR2基因中的等位基因与散发性绝经后乳腺癌风险相关。
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Genome-wide association study identifies novel breast cancer susceptibility loci.全基因组关联研究确定了新的乳腺癌易感基因座。
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