Hirata J, Abe Y, Taguchi F, Takatsuki H, Nishimura J, Nawata H
Department of Clinical Laboratory, Kyushu University Hospital, Fukuoka, Japan.
Cancer Genet Cytogenet. 1992 Feb;58(2):181-5. doi: 10.1016/0165-4608(92)90109-l.
Two cases of acute myeloblastic leukemia (AML M2) associated with a deletion of chromosome 6q are described. One was a 38-year-old man with constitutional inversion of chromosome 9, and another was a 57-year-old female atomic-bomb survivor. The karyotype of these patients were 46,XY,del(6)(q12q14),inv(9)(p11q13), and 47,XX,6q-,+min, respectively. In both cases c-myb protooncogene, which is located in chromosome 6q, was neither deleted nor rearranged, and c-myb messenger RNA level was not elevated. These results suggest that c-myb is not involved in the leukemogenesis of AML with 6q- as well as lymphoid malignancies with 6q-. Out of 23 AML cases with 6q- reviewed, 6 cases had erythroleukemia, and 4 developed in Down syndrome patients.
本文描述了两例与6号染色体长臂缺失相关的急性髓细胞白血病(AML M2)病例。一例为38岁男性,伴有9号染色体结构倒位;另一例为57岁女性原子弹幸存者。这两名患者的核型分别为46,XY,del(6)(q12q14),inv(9)(p11q13)和47,XX,6q-,+min。在这两例病例中,位于6号染色体长臂上的c-myb原癌基因既未缺失也未重排,且c-myb信使核糖核酸水平未升高。这些结果表明,c-myb不参与伴有6号染色体长臂缺失的急性髓细胞白血病的白血病发生过程,也不参与伴有6号染色体长臂缺失的淋巴系统恶性肿瘤的发生过程。在回顾的23例伴有6号染色体长臂缺失的急性髓细胞白血病病例中,6例为红白血病,其中4例发生于唐氏综合征患者。