European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case-control study in a high UV index region in Brazil
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | GONCALVES, Fernanda T. | |
dc.contributor.author | FRANCISCO, Guilherme | |
dc.contributor.author | SOUZA, Sonia P. de | |
dc.contributor.author | LUIZ, Olinda C. | |
dc.contributor.author | FESTA-NETO, Cyro | |
dc.contributor.author | SANCHES, Jose A. | |
dc.contributor.author | CHAMMAS, Roger | |
dc.contributor.author | GATTAS, Gilka J. F. | |
dc.contributor.author | ELUF-NETO, Jose | |
dc.date.accessioned | 2017-11-27T16:26:19Z | |
dc.date.available | 2017-11-27T16:26:19Z | |
dc.date.issued | 2011 | |
dc.description.abstract | Background: UV radiation is the major environmental factor related to development of cutaneous melanoma. Besides sun exposure and the influence of latitude, some host characteristics such as skin phototype and hair and eye color are also risk factors for melanoma. Polymorphisms in DNA repair genes could be good candidates for susceptibility genes, mainly in geographical regions exposed to high solar radiation. Objective: Evaluate the role of host characteristic.; and DNA repair polymorphism in melanoma risk in Brazil. Methods: We carried out a hospital-based case-control study in Brazil to evaluate the contribution of host factors and polymorphisms in DNA repair to melanoma risk. A total of 412 patients (202 with melanoma and 210 controls) were analyzed regarding host characteristics for melanoma risk as well as for 11 polymorphisms in DNA repair genes. Results: We found an association of host characteristics with melanoma development, such as eye and hair color, fair skin, history of pigmented lesions removed, sunburns in childhood and adolescence, and also European ancestry. Regarding DNA repair gene polymorphisms, we found protection for the XPG 1104 His/His genotype (OR 0.32; 95% CI 0.13-0.75), and increased risk for three polymorphisms in the XPC gene (PAT+; IV-6A and 939Gln), which represent a haplotype for XPC. Melanoma risk was higher in individuals carrying the complete XPC haplotype than each individual polymorphism (OR 3.64; 95% CI 1.77-7.48). Conclusions: Our data indicate that the host factors European ancestry and XPC polymorphisms contributed to melanoma risk in a region exposed to high sun radiation. | |
dc.description.index | MEDLINE | |
dc.description.sponsorship | Fundacao de Amparo a Pesquisa do Estado de Sao Paulo - FAPESP [06-52041-9, 05-56069-2] | |
dc.description.sponsorship | CNPq [478239/03-3] | |
dc.description.sponsorship | CNPq-Brazil | |
dc.identifier.citation | JOURNAL OF DERMATOLOGICAL SCIENCE, v.64, n.1, p.59-66, 2011 | |
dc.identifier.doi | 10.1016/j.jdermsci.2011.06.003 | |
dc.identifier.issn | 0923-1811 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/22949 | |
dc.language.iso | eng | |
dc.publisher | ELSEVIER IRELAND LTD | |
dc.relation.ispartof | Journal of Dermatological Science | |
dc.rights | restrictedAccess | |
dc.rights.holder | Copyright ELSEVIER IRELAND LTD | |
dc.subject | Melanoma | |
dc.subject | Case-control | |
dc.subject | DNA repair gene polymorphisms | |
dc.subject | XPC | |
dc.subject | Nucleotide excision repair | |
dc.subject.other | nucleotide excision-repair | |
dc.subject.other | cutaneous melanoma | |
dc.subject.other | ultraviolet-radiation | |
dc.subject.other | southern brazil | |
dc.subject.other | sun exposure | |
dc.subject.other | skin-cancer | |
dc.subject.other | xpd | |
dc.subject.other | association | |
dc.subject.other | damage | |
dc.subject.other | predisposition | |
dc.subject.wos | Dermatology | |
dc.title | European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case-control study in a high UV index region in Brazil | |
dc.type | article | |
dc.type.category | original article | |
dc.type.version | publishedVersion | |
dspace.entity.type | Publication | |
hcfmusp.author.external | SOUZA, Sonia P. de:Univ Sao Paulo, Fac Med, Dept Prevent Med, Lab Epidemiol Imunobiol LIM38, BR-01246903 Sao Paulo, Brazil | |
hcfmusp.citation.scopus | 32 | |
hcfmusp.contributor.author-fmusphc | FERNANDA DE TOLEDO GONCALVES | |
hcfmusp.contributor.author-fmusphc | GUILHERME FRANCISCO | |
hcfmusp.contributor.author-fmusphc | OLINDA DO CARMO LUIZ | |
hcfmusp.contributor.author-fmusphc | CYRO FESTA NETO | |
hcfmusp.contributor.author-fmusphc | JOSE ANTONIO SANCHES JUNIOR | |
hcfmusp.contributor.author-fmusphc | ROGER CHAMMAS | |
hcfmusp.contributor.author-fmusphc | GILKA JORGE FIGARO GATTAS | |
hcfmusp.contributor.author-fmusphc | JOSE ELUF NETO | |
hcfmusp.description.beginpage | 59 | |
hcfmusp.description.endpage | 66 | |
hcfmusp.description.issue | 1 | |
hcfmusp.description.volume | 64 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 21733660 | |
hcfmusp.origem.scopus | 2-s2.0-80052375957 | |
hcfmusp.origem.wos | WOS:000295192400009 | |
hcfmusp.publisher.city | CLARE | |
hcfmusp.publisher.country | IRELAND | |
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hcfmusp.scopus.lastupdate | 2024-05-10 | |
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