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无证据表明GATA3基因rs570613单核苷酸多态性会改变乳腺癌风险。

No evidence that GATA3 rs570613 SNP modifies breast cancer risk.

作者信息

Johnatty Sharon E, Couch Fergus J, Fredericksen Zachary, Tarrell Robert, Spurdle Amanda B, Beesley Jonathan, Chen Xiaoqing, Gschwantler-Kaulich Daphne, Singer Christian F, Fuerhauser Christine, Fink-Retter Anneliese, Domchek Susan M, Nathanson Katherine L, Pankratz Vernon S, Lindor Noralane M, Godwin Andrew K, Caligo Maria A, Hopper John, Southey Melissa C, Giles Graham G, Justenhoven Christina, Brauch Hiltrud, Hamann Ute, Ko Yon-Dschun, Heikkinen Tuomas, Aaltonen Kirsimari, Aittomäki Kristiina, Blomqvist Carl, Nevanlinna Heli, Hall Per, Czene Kamila, Liu Jianjun, Peock Susan, Cook Margaret, Platte Radka, Gareth Evans D, Lalloo Fiona, Eeles Rosalind, Pichert Gabriella, Eccles Diana, Davidson Rosemarie, Cole Trevor, Cook Jackie, Douglas Fiona, Chu Carol, Hodgson Shirley, Paterson Joan, Hogervorst Frans B L, Rookus Matti A, Seynaeve Caroline, Wijnen Juul, Vreeswijk Maaike, Ligtenberg Marjolijn, van der Luijt Rob B, van Os Theo A M, Gille Hans J P, Blok Marinus J, Issacs Claudine, Humphreys Manjeet K, McGuffog Lesley, Healey Sue, Sinilnikova Olga, Antoniou Antonis C, Easton Douglas F, Chenevix-Trench Georgia

机构信息

Cancer and Cell Biology, Queensland Institute of Medical Research, c/o Royal Brisbane Hospital Post Office, Herston, Brisbane, QLD 4029, Australia.

出版信息

Breast Cancer Res Treat. 2009 Sep;117(2):371-9. doi: 10.1007/s10549-008-0257-1. Epub 2008 Dec 11.

Abstract

GATA-binding protein 3 (GATA3) is a transcription factor that is crucial to mammary gland morphogenesis and differentiation of progenitor cells, and has been suggested to have a tumor suppressor function. The rs570613 single nucleotide polymorphism (SNP) in intron 4 of GATA3 was previously found to be associated with a reduction in breast cancer risk in the Cancer Genetic Markers of Susceptibility project and in pooled analysis of two case-control studies from Norway and Poland (P (trend) = 0.004), with some evidence for a stronger association with estrogen receptor (ER) negative tumours [Garcia-Closas M et al. (2007) Cancer Epidemiol Biomarkers Prev 16:2269-2275]. We genotyped GATA3 rs570613 in 6,388 cases and 4,995 controls from the Breast Cancer Association Consortium (BCAC) and 5,617 BRCA1 and BRCA2 carriers from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA). We found no association between this SNP and breast cancer risk in BCAC cases overall (OR(per-allele) = 1.00, 95% CI 0.94-1.05), in ER negative BCAC cases (OR(per-allele) = 1.02, 95% CI 0.91-1.13), in BRCA1 mutation carriers RR(per-allele) = 0.99, 95% CI 0.90-1.09) or BRCA2 mutation carriers (RR(per-allele) = 0.93, 95% CI 0.80-1.07). We conclude that there is no evidence that either GATA3 rs570613, or any variant in strong linkage disequilibrium with it, is associated with breast cancer risk in women.

摘要

GATA结合蛋白3(GATA3)是一种转录因子,对乳腺形态发生和祖细胞分化至关重要,并且有人认为它具有肿瘤抑制功能。先前在癌症易感性基因标记项目以及对来自挪威和波兰的两项病例对照研究的汇总分析中发现,GATA3第4内含子中的rs570613单核苷酸多态性(SNP)与乳腺癌风险降低相关(P(趋势)=0.004),有一些证据表明其与雌激素受体(ER)阴性肿瘤的关联更强[加西亚 - 克洛萨斯M等人(2007年)《癌症流行病学、生物标志物与预防》16:2269 - 2275]。我们对来自乳腺癌协会联盟(BCAC)的6388例病例和4995例对照以及来自BRCA1/2修饰因子研究联盟(CIMBA)的5617例BRCA1和BRCA2携带者的GATA3 rs570613进行了基因分型。我们发现,在BCAC总体病例中(每等位基因的比值比(OR)=1.00,95%置信区间0.94 - 1.05)、ER阴性的BCAC病例中(每等位基因的OR =1.02,95%置信区间0.91 - 1.13)、BRCA1突变携带者中(每等位基因的相对风险(RR)=0.99,95%置信区间0.90 - 1.09)或BRCA2突变携带者中(每等位基因的RR =0.93,95%置信区间0.80 - 1.07),该SNP与乳腺癌风险均无关联。我们得出结论,没有证据表明GATA3 rs570613或与之处于强连锁不平衡的任何变体与女性乳腺癌风险相关。

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