Title of article
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
Author/Authors
Park، نويسنده , , Tae-Sung and Lee، نويسنده , , Seung Tae and Song، نويسنده , , Jaewoo and Lee، نويسنده , , Kyung-A and Lee، نويسنده , , Jong Han and Kim، نويسنده , , Juwon and Lee، نويسنده , , Hyeon-Ji and Han، نويسنده , , Jeong-Hyun and Kim، نويسنده , , Jong-Kee and Cho، نويسنده , , Sung Ran and Choi، نويسنده , , Jong Rak، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2009
Pages
6
From page
87
To page
92
Abstract
We 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.
Journal title
Cancer Genetics and Cytogenetics
Serial Year
2009
Journal title
Cancer Genetics and Cytogenetics
Record number
1829519
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