融合基因
髓系白血病
嵌合基因
荧光原位杂交
白血病
基因
全血细胞减少症
医学
融合转录本
底漆(化妆品)
分子生物学
癌症研究
生物
遗传学
骨髓
免疫学
基因表达
染色体
化学
有机化学
作者
Sae Utsumi,Takahiro Shima,Chiaki Kubara,Yuichiro Semba,Morito Hayashi,Ken Takigawa,Teruhiko Yoshino,Mariko Minami,Yoko Matsuo,Takuro Kuriyama,Koichi Akashi,Takahiro Maeda,Shuichi Taniguchi,Tetsuya Eto
出处
期刊:PubMed
日期:2023-01-01
卷期号:64 (12): 1503-1507
标识
DOI:10.11406/rinketsu.64.1503
摘要
A 27-year-old woman with pancytopenia was admitted to our hospital. Bone marrow aspiration revealed 52.2% myeloperoxidase-positive myeloblasts, leading to a diagnosis of acute myeloid leukemia. While a screening test for chimeric genes related to leukemia initially yielded negative results, including for the CBFB::MYH11 fusion gene, G-banded karyotyping uncovered the presence of inv (16)(p13.1q22). Further investigation by fluorescence in situ hybridization (FISH) confirmed the split signals for CBFB. A second screening test for leukemia-related chimeric genes with different PCR primers revealed the elusive CBFB::MYH11 fusion gene. Subsequently, the type I CBFB::MYH11 fusion gene was identified through exhaustive exploration using RNA sequencing for fusion gene discovery. This exceptional case highlights the existence of a distinctive subtype of CBFB::MYH11 that may yield false-negative results in conventional chimeric fusion screening, thus emphasizing the indispensable utility of PCR primer modification, FISH, and RNA sequencing in the investigative process.
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