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The VEGF_936_C>T 3′UTR polymorphism reduces BRCA1-associated breast cancer risk in Polish women

2008; Elsevier BV; Volume: 262; Issue: 1 Linguagem: Inglês

10.1016/j.canlet.2007.11.029

1872-7980

Anna Jakubowska, Jacek Gronwald, Janusz Menkiszak, Bohdan Górski, Tomasz Huzarski, Tomasz Byrski, Lutz Edler, Jan Lubiński, Rodney J. Scott, Ute Hamann,

Bioinformatics and Genomic Networks

The vascular endothelial growth factor (VEGF) plays a crucial role in the initiation of angiogenesis, which is an important stage in tumor development. A functional 936_C>T polymorphism in the VEGF gene and its association with sporadic breast cancer risk has been analyzed in various studies yielding conflicting results. To analyze the role of this polymorphism in modifying hereditary breast and ovarian cancer risks, we conducted a case–control study and genotyped 755 Polish BRCA1 carriers, including 319 breast cancer cases, 146 ovarian cancer cases, and 290 unaffected controls. The results revealed an association of the CT + TT genotypes with a reduced breast cancer risk (ORadj 0.63, 95% CI, 0.41–0.98; ORclustered 0.63, 95% CI, 0.48–0.83), and a potential effect on ovarian cancer risk (ORadj 0.62, 95% CI, 0.33–1.18; ORclustered 0.62, 95% CI, 0.47–0.83). Thus, the 936_C>T polymorphism appears to modify disease risks in BRCA1 carriers.