Cimino G, Lanza C, Elia L, Lo Coco F, Gaidano G, Biondi A, Pastore C, Serra A, Canaani E, Croce C M, Mandelli F, Saglio G
Ematologia, Dipartimento di Biopatologia Umana, Universtità degli Studi La Sapienza di Roma, Rome, Italy.
Br J Haematol. 1997 Feb;96(2):308-13. doi: 10.1046/j.1365-2141.1997.d01-2044.x.
In this study we investigated the presence of structural lesions in the ALL-1, p53 and p16 (cyclin-dependent kinase 4 inhibitor) genes in leukaemic cells obtained from 22 patients with infant acute leukaemia (aged < 18 months). Of these, 18 cases were classified as acute lymphoblastic leukaemia (ALL) and four as acute myeloid leukaemia (AML). Tumour DNAs were analysed by a combination of Southern blot. polymerase chain reaction (PCR), single-strand conformation polymorphism (SSCP), and direct sequence analyses. The results showed ALL-1 gene rearrangements in 15/22 (68%) cases, p53 gene mutations in 5/22 (26%), and a homozygous deletion of p16 in a single T-ALL case. p53 and p16 alterations were all found in the group of patients with ALL-1 gene rearrangements. p53 mutations were more often associated with a myeloid phenotype (3/5). In summary, multiple molecular alterations were found in 6/15 (40%) infant acute leukaemias with ALL-1 rearrangements. As to the clinical course, patients with additional lesions had similar clinical outcome with respect to patients with ALL-1 gene rearrangement as the sole genetic aberration. This may support the hypothesis that ALL-1 alterations are genetic events per se sufficient to confer a fully malignant phenotype to the leukaemic clone.
在本研究中,我们调查了从22例婴儿急性白血病(年龄<18个月)患者获得的白血病细胞中ALL-1、p53和p16(细胞周期蛋白依赖性激酶4抑制剂)基因的结构损伤情况。其中,18例被分类为急性淋巴细胞白血病(ALL),4例为急性髓细胞白血病(AML)。通过Southern印迹、聚合酶链反应(PCR)、单链构象多态性(SSCP)和直接序列分析相结合的方法对肿瘤DNA进行分析。结果显示,22例中有15例(68%)存在ALL-1基因重排,22例中有5例(26%)存在p53基因突变,1例T-ALL病例中存在p16纯合缺失。p53和p16改变均在ALL-1基因重排的患者组中发现。p53突变更常与髓系表型相关(3/5)。总之,在15例ALL-1重排的婴儿急性白血病中有6例(40%)发现了多种分子改变。至于临床病程,有额外损伤的患者与仅有ALL-1基因重排这一唯一遗传异常的患者相比,临床结局相似。这可能支持以下假设:ALL-1改变本身就是足以赋予白血病克隆完全恶性表型的遗传事件。