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Detection of a novel CBFB/MYH11 variant fusion transcript (K-type) showing partial insertion of exon 6 of CBFB gene using two commercially available multiplex RT-PCR kits.

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dc.contributor.authorPark, TS-
dc.contributor.authorLee, ST-
dc.contributor.authorSong, J-
dc.contributor.authorLee, KA-
dc.contributor.authorLee, JH-
dc.contributor.authorKim, J-
dc.contributor.authorLee, HJ-
dc.contributor.authorHan, JH-
dc.contributor.authorKim, JK-
dc.contributor.authorCho, SR-
dc.contributor.authorChoi, JR-
dc.date.accessioned2010-11-25T06:54:39Z-
dc.date.available2010-11-25T06:54:39Z-
dc.date.issued2009-
dc.identifier.issn0165-4608-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/304-
dc.description.abstractWe report on a 20-year-old man with acute myeloid leukemia (AML) showing a distinct novel CBFB/MYH11 variant fusion transcript. Initial results of bone marrow, chromosome, and flow cytometric analyses were not in accordance with the diagnosis of acute myelomonocytic leukemia with eosinophilia (AML-M4Eo) or AML with a CBFB/MYH11 rearrangement. However, results from 2 commercially available multiplex reverse transcriptase-polymerase chain reaction (RT-PCR) tests repeatedly showed an unusual PCR product from his bone marrow specimen. Not only does this case show a partial insertion of exon 6 of the CBFB (ENSG00000067955) gene, but it also involves novel breakpoints within both exon 6 of the CBFB gene and exon 28 (previously exon 7) of the MYH11 (ENSG00000133392) gene, which is regarded as a previously non-reported, new type (K-type) of CBFB/MYH11 fusion transcript. In addition, our study result was in agreement with the recent report of Schnittger et al. that rare fusion transcripts of CBFB/MYH11 are correlated with an atypical cytomorphology and other aberrant characteristics. Therefore, multiplex RT-PCR and sequence analysis of these atypical products should be performed to diagnose atypical AML with CBFB/MYH11 rearrangement, to predict prognosis of these patients as well as to elucidate the molecular mechanism.-
dc.formattext/plain-
dc.language.isoen-
dc.subject.MESHBase Sequence-
dc.subject.MESHCore Binding Factor beta Subunit-
dc.subject.MESHCytogenetic Analysis-
dc.subject.MESHDNA Mutational Analysis-
dc.subject.MESHExons-
dc.subject.MESHGenes, Neoplasm-
dc.subject.MESHHumans-
dc.subject.MESHLeukemia, Myeloid, Acute-
dc.subject.MESHMale-
dc.subject.MESHMolecular Sequence Data-
dc.subject.MESHMutagenesis, Insertional-
dc.subject.MESHMyosin Heavy Chains-
dc.subject.MESHReagent Kits, Diagnostic-
dc.subject.MESHRecombinant Fusion Proteins-
dc.subject.MESHReverse Transcriptase Polymerase Chain Reaction-
dc.subject.MESHYoung Adult-
dc.titleDetection of a novel CBFB/MYH11 variant fusion transcript (K-type) showing partial insertion of exon 6 of CBFB gene using two commercially available multiplex RT-PCR kits.-
dc.typeArticle-
dc.identifier.pmid19215788-
dc.identifier.urlhttp://linkinghub.elsevier.com/retrieve/pii/S0165-4608(08)00624-9-
dc.contributor.affiliatedAuthor조, 성란-
dc.type.localJournal Papers-
dc.identifier.doi10.1016/j.cancergencyto.2008.10.012-
dc.citation.titleCancer genetics and cytogenetics-
dc.citation.volume189-
dc.citation.number2-
dc.citation.date2009-
dc.citation.startPage87-
dc.citation.endPage92-
dc.identifier.bibliographicCitationCancer genetics and cytogenetics, 189(2). : 87-92, 2009-
dc.identifier.eissn1873-4456-
dc.relation.journalidJ001654608-
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Journal Papers > School of Medicine / Graduate School of Medicine > Laboratory Medicine
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