Stock W, Thirman M J, Dodge R K, Rowley J D, Diaz M O, Wurster-Hill D, Sobol R E, Davey F R, Larson R A, Westbrook C A
Department of Medicine and Cancer Research Center, University of Chicago, IL.
Leukemia. 1994 Nov;8(11):1918-22.
Specific structural rearrangements involving chromosome band 11q23 occur in a variety of hematologic malignancies, including an estimated 2-7% of patients with acute lymphoblastic leukemia (ALL). Translocations involving chromosome band 11q23 have been associated with a poor prognosis in patients with ALL. Recently, a gene known as MLL has been identified which is involved in acute lymphoid and myeloid leukemias with rearrangements at 11q23. A 0.74-kilobase (kb) cDNA probe from the MLL gene can detect both common and uncommon rearrangements involving MLL on conventional Southern blots. We studied 86 newly diagnosed adults entered on an ALL clinical trial to investigate the incidence of MLL gene rearrangements and to determine clinical, morphologic, immunologic and cytogenetic characteristics of such patients. Two of 86 patients had MLL gene rearrangements detected by Southern blot analysis. One of these 86 patients had an 11q23 translocation by cytogenetic analysis whereas the second patient was unevaluable by standard cytogenetic analysis. Southern blot identification of rearrangements involving MLL, especially in patients with limited material for cytogenetic analysis, can provide critical diagnostic and prognostic information which may be useful in the clinical management of patients with these abnormalities.
涉及染色体带11q23的特定结构重排在多种血液系统恶性肿瘤中出现,包括估计2%至7%的急性淋巴细胞白血病(ALL)患者。涉及染色体带11q23的易位与ALL患者的不良预后相关。最近,一种名为MLL的基因已被鉴定出来,它参与了11q23发生重排的急性淋巴细胞和髓细胞白血病。来自MLL基因的一个0.74千碱基(kb)的cDNA探针可以在传统的Southern印迹上检测涉及MLL的常见和罕见重排。我们研究了86名新诊断的参加ALL临床试验的成年人,以调查MLL基因重排的发生率,并确定此类患者的临床、形态学、免疫学和细胞遗传学特征。86名患者中有2名通过Southern印迹分析检测到MLL基因重排。这86名患者中的1名通过细胞遗传学分析有11q23易位,而第二名患者无法通过标准细胞遗传学分析进行评估。通过Southern印迹鉴定涉及MLL的重排,特别是在细胞遗传学分析材料有限的患者中,可以提供关键的诊断和预后信息,这可能对这些异常患者的临床管理有用。