Pui C H, Raskind W H, Kitchingman G R, Raimondi S C, Behm F G, Murphy S B, Crist W M, Fialkow P J, Williams D L
Department of Hematology-Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee 38101.
J Clin Invest. 1989 Jun;83(6):1971-7. doi: 10.1172/JCI114106.
Acute lymphoblastic leukemia (ALL) is generally regarded as a clonal disease in which a single abnormal progenitor cell gives rise to neoplastic progeny. Five of 463 cases of childhood ALL with adequately banded leukemic cells were found to have two cytogenetically independent cell populations. In addition, two of the four cases tested had more than two rearranged immunoglobulin genes and (or) T cell receptor genes. To investigate the clonality of these unusual leukemias, we examined the neoplastic cells for X-linked markers extrinsic to the disease. Leukemic cells from each of the three patients heterozygous for an X-linked, restriction fragment length polymorphism showed a single active parental allele, suggesting that both apparently independent cell populations developed from a common progenitor. These cases provide evidence that leukemogenesis involves a multistep process of mutation and suggest that karyotypic abnormalities may be a late event of malignant transformation.
急性淋巴细胞白血病(ALL)通常被视为一种克隆性疾病,其中单个异常祖细胞产生肿瘤后代。在463例白血病细胞带型分析充分的儿童ALL病例中,有5例被发现有两个细胞遗传学上独立的细胞群体。此外,检测的4例病例中有2例有两个以上重排的免疫球蛋白基因和(或)T细胞受体基因。为了研究这些不寻常白血病的克隆性,我们检查了肿瘤细胞中该疾病以外的X连锁标记。三名X连锁限制性片段长度多态性杂合的患者的白血病细胞均显示单个活跃的亲本等位基因,这表明两个明显独立的细胞群体均由一个共同的祖细胞发育而来。这些病例提供了白血病发生涉及多步骤突变过程的证据,并表明核型异常可能是恶性转化的晚期事件。