Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/45053

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dc.contributor.authorCárcano, Flavio Mavignierpor
dc.contributor.authorVidal, Daniel Onofrepor
dc.contributor.authorLengert, André van Helvoortpor
dc.contributor.authorScapulatempo-Neto, Cristovampor
dc.contributor.authorQueiroz, Luisapor
dc.contributor.authorMarques, Herlanderpor
dc.contributor.authorBaltazar, Fátimapor
dc.contributor.authorMartinelli, Camila Maria da Silvapor
dc.contributor.authorSoares, Paulapor
dc.contributor.authorReis, R. M.por
dc.contributor.other[et al.]-
dc.date.accessioned2017-03-16T13:45:28Z-
dc.date.issued2016-
dc.identifier.citationCárcano, F. M., Vidal, D. O., van Helvoort Lengert, A., Neto, C. S., Queiroz, L., Marques, H., . . . Reis, R. M. (2016). Hotspot TERT promoter mutations are rare events in testicular germ cell tumors. [Article]. Tumor Biology, 37(4), 4901-4907. doi: 10.1007/s13277-015-4317-y-
dc.identifier.issn1010-4283por
dc.identifier.urihttps://hdl.handle.net/1822/45053-
dc.description.abstractThe abnormal activation of telomerase, codified by the telomerase reverse transcriptase (TERT) gene, is related to one of cancer hallmarks. Hotspot somatic mutations in the promoter region of TERT, specifically the c.-124:C > T and c.-146:C > T, were recently identified in a range of human cancers and have been associated with a more aggressive behavior. Testicular germ cell tumors frequently exhibit a good prognosis; however, the development of refractory disease is still a clinical challenge. In this study, we aim to evaluate for the first time the presence of the hotspot telomerase reverse transcriptase gene promoter mutations in testicular germ cell tumors. A series of 150 testicular germ cell tumor cases and four germ cell tumor cell lines were evaluated by PCR followed by direct Sanger sequencing and correlated with patient's clinical pathological features. Additionally, we genotyped the telomerase reverse transcriptase gene promoter single nucleotide polymorphism rs2853669 (T > C) located at -245 position. We observed the presence of the TERT promoter mutation in four patients, one exhibited the c.-124:C > T and three the c.-146:C > T. No association between TERT mutation status and clinicopathological features could be identified. The analysis of the rs2853669 showed that variant C was present in 22.8 % of the cases. In conclusion, we showed for the first time that TERT promoter mutations occur in a small subset (similar to 3 %) of testicular germ cell tumors.por
dc.description.sponsorshipThis work was supported by the Barretos Cancer Hospital internal research funds (PAIP): Project “Microenvironment, metabolism and cancer” that was partially supported by Programa Operacional Regional do Norte (ON.2 – O Novo Norte), under the Quadro de Referência Estratégico Nacional (QREN), and through the Fundo Europeu de Desenvolvimento Regional (FEDER). R.M.R. has a National Counsel of Technological and Scientific Development (CNPq) scholarship.por
dc.language.isoengpor
dc.publisherSpringerpor
dc.rightsclosedAccesspor
dc.subjectTesticular neoplasmspor
dc.subjectNeoplasms, germ cell, and embryonalpor
dc.subjectTERT proteinpor
dc.subjectMutationpor
dc.subjectPolymorphism, single nucleotidepor
dc.titleHotspot TERT promoter mutations are rare events in testicular germ cell tumorspor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttp://link.springer.com/article/10.1007%2Fs13277-015-4317-ypor
sdum.publicationstatuspublished-
oaire.citationStartPage4901por
oaire.citationEndPage4907por
oaire.citationIssue4por
oaire.citationTitleTumor Biologypor
oaire.citationVolume37por
dc.date.updated2017-03-10T13:04:28Z-
dc.identifier.doi10.1007/s13277-015-4317-ypor
dc.identifier.pmid26526580por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersionpor
dc.subject.wosScience & Technologypor
sdum.journalTumor Biologypor
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

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