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dc.creatorVageli, D.en
dc.creatorDaniil, Z.en
dc.creatorDahabreh, J.en
dc.creatorKaragianni, E.en
dc.creatorLiloglou, T.en
dc.creatorKoukoulis, G.en
dc.creatorGourgoulianis, K.en
dc.date.accessioned2015-11-23T10:53:01Z
dc.date.available2015-11-23T10:53:01Z
dc.date.issued2006
dc.identifier.issn1021-335X
dc.identifier.urihttp://hdl.handle.net/11615/34212
dc.description.abstractThe possible causes and genetic mechanisms of pulmonary carcinoid tumor development are unclear. In this study, we examined genetic alterations at the MEN1 locus in archival material from 15 pulmonary carcinoids. We employed, for the first time in this setting, real-time PCR with melting curve analysis in order to identify loss of heterozygosity (LOH) or microsatellite instability (MI) in two polymorphic markers (PYGM, D11S449) at the MEN1 locus and one additional marker (D11S906) of a putative oncosuppressive region distal to the MEN1 gene. Sequencing data were available in a selected subset of tumors in order to verify the reliability of real-time PCR analysis. We observed LOH at PYGM in 38% of the cases and MI in 13.3% of the cases. Our data indicate that real-time PCR with melting curve analysis is a reliable technique for LOH and MI detection and indicate that genetic errors at the MEN1 locus but also distal to it may be involved in the development of sporadic pulmonary carcinoid tumors.en
dc.sourceOncology Reportsen
dc.source.uri<Go to ISI>://WOS:000235317700007
dc.subjectMEN1en
dc.subjectLOHen
dc.subjectmicrosatellite instabilityen
dc.subjectlung carcinoidsen
dc.subjectreal-time PCRen
dc.subjectENDOCRINE-NEOPLASIA TYPE-1en
dc.subjectSUPPRESSOR GENEen
dc.subjectPARATHYROID TUMORSen
dc.subjectALLELICen
dc.subjectDELETIONSen
dc.subjectPITUITARY-TUMORSen
dc.subjectCHROMOSOME 11Q13en
dc.subjectMUTATIONSen
dc.subjectLOCALIZATIONen
dc.subjectREGIONen
dc.subjectOncologyen
dc.titleMicrosatellite instability and loss of heterozygosity at the MEN1 locus in lung carcinoid tumors: A novel approach using real-time PCR with melting curve analysis in histopathologic materialen
dc.typejournalArticleen


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