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dc.contributor.author Fassan, Matteo
dc.contributor.author Baffa, Raffaele
dc.contributor.author Kiss, András
dc.contributor.author Zaninotto, Giovanni
dc.contributor.author Rugge, Massimo
dc.date.accessioned 2016-09-27T09:43:27Z
dc.date.available 2016-09-27T09:43:27Z
dc.date.issued 2013
dc.identifier.citation pagination=1236-1241; journalVolume=19; journalIssueNumber=7; journalTitle=CURRENT PHARMACEUTICAL DESIGN;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3436
dc.description.abstract While the phenotypic changes involved in the esophageal oncogenic "cascade" are now well established, the molecular profiling of this pathway remains unreliable. Our understanding of the molecular dysregulations underlying the development/progression of cancer has recently been expanded by the characterization of a new class of small, noncoding RNA gene products, the microRNAs (or miRNAs). These "endogenous silencers" target a large number of genes, functioning as tumor suppressors or tumor promoters, depending on the activity of the targeted genes. In esophageal cancer, miRNA dysregulation plays a significant part in the molecular oncogenic pathway, in cancer prognosis, and in patients' responsiveness to neo-adjuvant and adjuvant therapies. In addition to these valuable features, miRNAs have been proposed as innovative therapeutics per se and as plausible biological targets in new treatment strategies.
dc.relation.ispartof urn:issn:1381-6128
dc.title MicroRNA Dysregulation in Esophageal Neoplasia: The Biological Rationale for Novel Therapeutic Options
dc.type Journal Article
dc.date.updated 2016-06-08T12:11:15Z
dc.language.rfc3066 en
dc.identifier.mtmt 2234878
dc.identifier.wos 000316451800007
dc.identifier.pubmed 23092347
dc.contributor.department SE/AOK/I/II. Sz. Patológiai Intézet
dc.contributor.institution Semmelweis Egyetem


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