Xue Y, Yu F, Xin Y, Lu D, Zou Z, Guo Y, Xie X
Leukaemia Research Unit, Jiangsu Institute of Haematology, First Affiliated Hospital of Suzhou Medical College, PR China.
Br J Haematol. 1997 Sep;98(3):733-5. doi: 10.1046/j.1365-2141.1997.2693088.x.
A novel variant translocation t(8;20)(q22;p13) detected by karyotype analysis of bone marrow cells using R- and G-banding techniques, is reported in a case of M2-acute myeloid leukaemia (AML). The leukaemic cells were indistinguishable morphologically from that of M2-AML with t(8;21)translocation. RT-PCR revealed no AML1/ETO fusion transcript, but the wild-type ETO-3' was expressed in the bone marrow cells suggesting that t(8;20) is a true simple variant translocation of t(8;21), and that a fusion gene consisting of ETO and an unidentified gene located in band 20p13 may exist in our case. Further study is required to clarify the entity of the assumed fusion gene.
在一例M2型急性髓系白血病(AML)中,报告了通过使用R带和G带技术对骨髓细胞进行核型分析检测到的一种新型变异易位t(8;20)(q22;p13)。白血病细胞在形态上与伴有t(8;21)易位的M2型AML细胞无法区分。逆转录聚合酶链反应(RT-PCR)未检测到AML1/ETO融合转录本,但野生型ETO-3'在骨髓细胞中表达,这表明t(8;20)是t(8;21)的一种真正的简单变异易位,并且在我们的病例中可能存在由ETO和位于20p13带的一个未鉴定基因组成的融合基因。需要进一步研究以阐明假定融合基因的实体。