Integrin β3 Leu33Pro polymorphism increases BRCA1-associated ovarian cancer risk

被引:11
作者
Jakubowska, Anna
Gronwald, Jacek
Menkiszak, Janusz
Gorski, Bohdan
Huzarski, Tomasz
Byrski, Tomasz
Edler, Lutz
Lubinski, Jan
Scott, Rodney J.
Hamann, Ute
机构
[1] German Canc Res Ctr, Div Mol Genome Anal Mol Genet Breast Canc, D-69120 Heidelberg, Germany
[2] Pomeranian Med Univ, Dept Genet & Pathol, Int Hereditary Canc Ctr, Szczecin, Poland
[3] Pomeranian Med Univ, Dept Surg Gynecol & Gynecol Oncol Adulst & Adoles, Szczecin, Poland
关键词
PLATELET GLYCOPROTEIN-IIIA; ACTIVATED PROTEIN-KINASE; BREAST-CANCER; BRCA1; ALPHA-V-BETA-3; MUTATIONS; CELLS; OOPHORECTOMY; HOMOZYGOSITY; ASSOCIATION;
D O I
10.1136/jmg.2006.047498
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Integrins are heterodimeric transmembrane glycoproteins that function as key adhesion and cell signalling receptors. A functional polymorphism in the integrin beta 3 subunit encoded by the ITGB3 gene, Leu33Pro, has been shown to modify a variety of traits of beta 3-expressing cells. To analyse the role of this functional polymorphism in modifying BRCA1-associated ovarian and breast cancer risks, a case - control study was performed among Polish BRCA1 mutation carriers including 319 breast cancer cases, 146 ovarian cancer cases and 290 controls unaffected by breast and ovarian cancer, in situ breast cancer or any other kind of cancer. Genotyping analysis was performed using PCR- based restriction fragment length polymorphism analysis. Odds ratios were calculated using univariate and multivariate logistic regression, taking into account a series of confounding variables, including the presence of related study subjects, that potentially could have biased any association. The results revealed that the ITGB3_ Leu33Pro polymorphism was associated with a 2.5- fold increased risk of ovarian cancer, whereas no association with breast cancer risk was found. Thus, it appears that the ITGB3_ Leu33Pro polymorphism may potentially increase the risk of ovarian cancer in Polish women with an inherited BRCA1 mutation.
引用
收藏
页码:408 / 411
页数:4
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