| Literature DB >> 22571796 |
Silvana Aparecida Alves Correa-Noronha1, Samuel Marcos Ribeiro de Noronha, Cheryl Alecrim, Adriana de Carvalho Mesquita, Gabriela Soares da Silva Brito, Michele Gilvana Junqueira, Daniela Batista Leite, Cristina Valletta de Carvalho, Ismael Dale Cotrim Guerreiro da Silva.
Abstract
Associations have been found between the angiotensin-converting enzyme insertion deletion (I/D) polymorphism (ACE I/D) and endometrial and epithelial ovarian cancer (EC and EOC, respectively). In this study, the following frequencies for each of three ACE polymorphisms, DD, ID, and II, respectively, were observed: in the EC group, 55, 24, and 21% versus the control group 39, 40, and 21% (p = 0.033*); in the EOC group 49, 36, and 15% versus the control group 49, 33, and 18% (p = 0.82). According to these allelic distributions, DD carriers are 2.0 times more likely than individuals carrying the ID or II genotypes to develop EC; therefore, the DD genotype seems to be protective against EC. In contrast, no association was observed between ACE (I/D) polymorphism with EOC. The ACE (I/D) polymorphism might play a role in the pathogenesis of EC and it should be considered when identifying genetic markers for EC.Entities:
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Year: 2012 PMID: 22571796 DOI: 10.3109/09513590.2012.683060
Source DB: PubMed Journal: Gynecol Endocrinol ISSN: 0951-3590 Impact factor: 2.260