PON1 Q192R polymorphism (rs662) is associated with childhood embryonal tumors

dc.TypeArticlept_BR
dc.contributor.authorVasconcelos, Gisele Moledo de
dc.contributor.authorAzevedo, Rafaela Montalvão de
dc.contributor.authorThuler, Luiz Claudio Santos
dc.contributor.authorBraga, Flavio Henrique Paraguassu
dc.contributor.authorPombo-de-Oliveira, Maria do Socorro
dc.contributor.authorCamargo, Beatriz de
dc.contributor.authorGonçalves, Bruno Alves de Aguiar
dc.date.accessioned2022-05-13T18:54:17Z
dc.date.available2022-05-13T18:54:17Z
dc.date.issued2014
dc.descriptionp. 6111–6115.: tab. p&b.
dc.description.abstractGenetic susceptibility and environment expo sures are associated risk factors in carcinogenesis. Gene polymorphisms that decrease the activity of detoxifying carcinogen substances may modify the effect of exposures. We investigated whether the polymorphisms PON1 rs662 (Q192R), and PON1 rs854560 (L55M) would be associated with embryonal tumors in Brazilian children. Blood sam ples from 163 children with embryonal tumors and 342 as control group were genotyped by TaqMAN real-time PCR assays. Logistic regression was used to evaluate the asso ciation between the polymorphisms of cases and controls groups, adjusted by skin color and age strata. When all tumors were taken together, the presence of the PON1 rs662 (Q192R) variant genotype (RR) was associated with an increased risk of developing embryonal tumors (OR = 2.80, 95 % CI 1.12–7.02). The presence of at least one variant PON1 rs662 R allele increased the risk of developing Wilms´ Tumor although without statistical power. However, it was observed a significant association of PON1 rs662 (Q192R) variant genotype (RR) with reti noblastoma (OR = 4.08, 95 % CI 1.13–14.97), whereas the PON1 rs854560 (L55M) polymorphism was not asso ciated with any tumor. These results indicate that PON1 polymorphisms may have an influence on the risk of developing embryonal tumors.
dc.identifier.citationVASCONCELOS, Gisele Moledo de et al. PON1 Q192R polymorphism (rs662) is associated with childhood embryonal tumors. Mol Biol Rep., v. 41, p. 6111–6115, 2014.
dc.identifier.issn1573-4978
dc.identifier.urihttp://sr-vmlxaph03:8080/jspui/handle/123456789/6930
dc.publisherMol Biol Reppt_BR
dc.subjectNeoplasias Embrionárias de Células Germinativaspt_BR
dc.subjectNeoplasms Germ Cell and Embryonalpt_BR
dc.subjectPredisposição Genética para Doençapt_BR
dc.subjectGenetic Predisposition to Diseasept_BR
dc.subjectPolimorfismo Genéticopt_BR
dc.subjectPolymorphism Geneticpt_BR
dc.subjectTumor de Wilmspt_BR
dc.subjectWilms Tumorpt_BR
dc.subjectNeuroblastomapt_BR
dc.subjectRetinoblastomapt_BR
dc.titlePON1 Q192R polymorphism (rs662) is associated with childhood embryonal tumorspt_BR

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