Mutational profile of driver genes in Brazilian melanomas

dc.contributor.authorVicente, Anna Luiza S. A.por
dc.contributor.authorCrovador, Camila S.por
dc.contributor.authorMacedo, Grazielapor
dc.contributor.authorScapulatempo-Neto, Cristovampor
dc.contributor.authorReis, R. M.por
dc.contributor.authorVazquez, Vinicius L.por
dc.date.accessioned2020-10-08T15:53:59Z
dc.date.available2020-10-08T15:53:59Z
dc.date.issued2019-11
dc.description.abstractMutation testing of the key genes involved in melanoma oncogenesis is now mandatory for the application of targeted therapeutics. However, knowledge of the mutational profile of melanoma remains largely unknown in Brazil. PURPOSE Mutation testing of the key genes involved in melanoma oncogenesis is now mandatory for the application of targeted therapeutics. However, knowledge of the mutational profile of melanoma remains largely unknown in Brazil. PATIENTS AND METHODS In this study, we assessed the mutation status of melanoma driver genes BRAF, NRAS, TERT, KIT, and PDGFRA in a cohort of 459 patients attended at Barretos Cancer Hospital between 2001 and 2012. We used polymerase chain reaction followed by Sanger sequencing to analyze the hot spot mutations of BRAF exon 15 (V600E), NRAS (codons 12/13 and 61), TERT (promoter region), KIT (exons 9, 11, 13, and 17), and PDGFRA (exons 12, 14, and 18) in tumors. The mutational profile was investigated for associations with demographic, histopathologic, and clinical features of the disease. RESULTS The nodular subtype was most frequent (38.9%) followed by the superficial spreading subtype (34.4%). The most frequent tumor location was in the limbs (50.0%). The mutation rates were 34.3% for TERT and 34.1% for BRAF followed by NRAS (7.9%), KIT (6.2%), and PDGFRA (2.9%). The BRAF (P = .014) and TERT (P = .006) mutations were associated with younger patients and with different anatomic locations, particularly in the trunk, for the superficial spreading and nodular subtypes, respectively (P = .0001 for both). PDGFRA mutations were associated with black skin color (P = .023) and TERT promoter mutations with an absence of ulceration (P = .037) and lower levels of lactate dehydrogenase. There was no association between patient survival rates and mutational status. CONCLUSION The similar mutational profile we observe in melanomas in Brazil compared with other populations will help to guide precision medicine in this country.por
dc.description.sponsorshipCAPES -Coordenação de Aperfeiçoamento de Pessoal de Nível Superior(2012/04194-1)por
dc.distributioninternationalpor
dc.identifier.citationVicente, A. L. S., Crovador, C. S., Macedo, G., Scapulatempo-Neto, C., Reis, R. M., & Vazquez, V. L. (2019). Mutational Profile of Driver Genes in Brazilian Melanomas. Journal of global oncology, 5, 1-14por
dc.identifier.doi10.1200/JGO.19.00169por
dc.identifier.eissn2378-9506
dc.identifier.issn2378-9506por
dc.identifier.pmid31756131por
dc.identifier.urihttps://hdl.handle.net/1822/67402
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherAmerican Society of Clinical Oncologypor
dc.relation.publisherversionhttps://ascopubs.org/doi/full/10.1200/JGO.19.00169por
dc.rightsopenAccesspor
dc.subjectAdultpor
dc.subjectAgedpor
dc.subjectBrazilpor
dc.subjectFemalepor
dc.subjectGTP Phosphohydrolasespor
dc.subjectHumanspor
dc.subjectMalepor
dc.subjectMelanomapor
dc.subjectMembrane Proteinspor
dc.subjectMiddle Agedpor
dc.subjectMutationpor
dc.subjectPromoter Regions, Geneticpor
dc.subjectProto-Oncogene Proteins B-rafpor
dc.subjectProto-Oncogene Proteins c-kitpor
dc.subjectReceptor, Platelet-Derived Growth Factor alphapor
dc.subjectSkin Neoplasmspor
dc.subjectTelomerasepor
dc.subject.fosCiências Médicas::Medicina Básicapor
dc.subject.wosScience & Technologypor
dc.titleMutational profile of driver genes in Brazilian melanomaspor
dc.typearticlepor
dspace.entity.typePublicationen
oaire.citationEndPage14por
oaire.citationIssue5por
oaire.citationStartPage1por
oaire.citationVolume5por
sdum.journalJournal of Global Oncologypor

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