Ariyama Y, Fukuda Y, Okuno Y, Seto M, Date K, Abe T, Nakamura Y, Inazawa J
Laboratories of Genome Medicine, Institute of Medical Science, University of Tokyo, Japan.
Genes Chromosomes Cancer. 1998 Nov;23(3):267-72.
Partial-tandem duplication (PTD) of an internal portion of MLL occurs in some cases of acute myelogenous leukemia (AML) with trisomy 11 or a normal karyotype. This type of MLL rearrangement may be transcribed into an mRNA species that is capable of encoding a partially duplicated protein associated with leukemogenesis. However, although several kinds of oncogenes, especially MYC, are often amplified on double-minute chromosomes (dmins) in hematological malignancies, no amplification of MLL has been reported in AML. Here, we report the first documented case of a patient with AML whose leukemic cells exhibited amplification of MLL on dmins. Furthermore, in this patient, MLL was rearranged in a PTD manner, with in-frame fusion of exons 2 and 6.
MLL内部部分的部分串联重复(PTD)出现在一些伴有11号染色体三体或正常核型的急性髓系白血病(AML)病例中。这种类型的MLL重排可能转录成一种mRNA物种,其能够编码与白血病发生相关的部分重复蛋白。然而,尽管在血液系统恶性肿瘤中几种癌基因,尤其是MYC,经常在双微体染色体(dmins)上扩增,但在AML中尚未有MLL扩增的报道。在此,我们报告首例有文献记载的AML患者,其白血病细胞在dmins上表现出MLL扩增。此外,在该患者中,MLL以PTD方式重排,外显子2和6发生读码框内融合。