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dc.contributor.authorKuasne, Hellen-
dc.contributor.authorMarchi, Fabio Albuquerque-
dc.contributor.authorRogatto, Silvia Regina-
dc.contributor.authorde Syllos Cólus, Ilce Mara-
dc.date.accessioned2014-05-27T11:29:38Z-
dc.date.accessioned2016-10-25T18:49:08Z-
dc.date.available2014-05-27T11:29:38Z-
dc.date.available2016-10-25T18:49:08Z-
dc.date.issued2013-06-01-
dc.identifierhttp://dx.doi.org/10.3390/ijms140610791-
dc.identifier.citationInternational Journal of Molecular Sciences, v. 14, n. 6, p. 10791-10808, 2013.-
dc.identifier.issn1661-6596-
dc.identifier.issn1422-0067-
dc.identifier.urihttp://hdl.handle.net/11449/75587-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/75587-
dc.description.abstractPenile carcinoma (PeCa) represents an important public health problem in poor and developing countries. Despite its unpredictable behavior and aggressive treatment, there have only been a few reports regarding its molecular data, especially epigenetic mechanisms. The functional diversity in different cell types is acquired by chromatin modifications, which are established by epigenetic regulatory mechanisms involving DNA methylation, histone acetylation, and miRNAs. Recent evidence indicates that the dysregulation in these processes can result in the development of several diseases, including cancer. Epigenetic alterations, such as the methylation of CpGs islands, may reveal candidates for the development of specific markers for cancer detection, diagnosis and prognosis. There are a few reports on the epigenetic alterations in PeCa, and most of these studies have only focused on alterations in specific genes in a limited number of cases. This review aims to provide an overview of the current knowledge of the epigenetic alterations in PeCa and the promising results in this field. The identification of epigenetically altered genes in PeCa is an important step in understanding the mechanisms involved in this unexplored disease. © 2013 by the authors; licensee MDPI, Basel, Switzerland.en
dc.format.extent10791-10808-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectDNA methylation-
dc.subjectEpigenetic-
dc.subjectMolecular markers-
dc.subjectPenile cancer-
dc.subjectcyclin dependent kinase inhibitor 2A-
dc.subjectcytosine-
dc.subjectDNA-
dc.subjecthistone-
dc.subjectmicroRNA-
dc.subjectRas association domain family protein 1A-
dc.subjectcancer diagnosis-
dc.subjectcancer prognosis-
dc.subjectcancer risk-
dc.subjectcancer therapy-
dc.subjectCpG island-
dc.subjectepigenetics-
dc.subjectEpstein Barr virus-
dc.subjectEpstein Barr virus infection-
dc.subjecthistopathology-
dc.subjecthuman-
dc.subjectlymph node dissection-
dc.subjectlymph node metastasis-
dc.subjectnonhuman-
dc.subjectpapillomavirus infection-
dc.subjectpenis carcinoma-
dc.subjectprediction-
dc.subjectreview-
dc.subjectrisk factor-
dc.subjectWart virus-
dc.titleEpigenetic mechanisms in penile carcinomaen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)-
dc.contributor.institutionCIPE-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of General Biology Londrina State University, Londrina, PR 86055-900-
dc.description.affiliationInternational Research and Teaching Center CIPE, AC Camargo Cancer Center, São Paulo, SP 01508-010-
dc.description.affiliationInter-institutional Grad Program on Bioinformatics Institute of Mathematics and Statistics USP-São Paulo University, São Paulo, SP 05508-090-
dc.description.affiliationDepartment of Urology UNESP, Botucatu, SP 18618-970-
dc.description.affiliationUnespDepartment of Urology UNESP, Botucatu, SP 18618-970-
dc.identifier.doi10.3390/ijms140610791-
dc.identifier.wosWOS:000320772500007-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-84878174197.pdf-
dc.relation.ispartofInternational Journal of Molecular Sciences-
dc.identifier.scopus2-s2.0-84878174197-
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