Einhorn S, Grandér D, Björk O, Bröndum-Nielsen K, Söderhäll S
Division of Experimental Oncology, Radiumhemmet, Stockholm, Sweden.
Cancer Res. 1990 Dec 15;50(24):7781-5.
Scanning densitometry and restriction fragment length polymorphism analysis were used to study the alpha-, beta-, gamma-, and omega-interferon (IFN) genes in malignant cells from 11 children with acute lymphocytic leukemia and in one cell line of T-cell origin. In the malignant cells of one patient there was a complete loss of alpha-, beta-, and omega-IFN genes, whereas in another patient one of the alleles of these genes had been deleted. Cytogenetic analysis revealed a deletion of the short arm of chromosome 9, i.e., the region containing the alpha-, beta-, and omega-IFN genes, in the latter patient. The normal cells of the patients with IFN gene deletions had two alleles of the alpha-, beta-, and omega-IFN genes. In cells from none of the patients could deletions or rearrangements of the gamma-IFN genes be detected. We conclude that in 2 of 11 patients with acute lymphocytic leukemia the malignant transformation is accompanied by loss of material on one or both chromosomes 9 and that the alpha-, beta-, and omega-IFN genes are included in these deletions.
采用扫描光密度测定法和限制性片段长度多态性分析,对11例急性淋巴细胞白血病患儿的恶性细胞以及1株T细胞来源的细胞系中的α、β、γ和ω干扰素(IFN)基因进行了研究。在1例患者的恶性细胞中,α、β和ω干扰素基因完全缺失,而在另1例患者中,这些基因的一个等位基因发生了缺失。细胞遗传学分析显示,后1例患者的9号染色体短臂发生了缺失,即包含α、β和ω干扰素基因的区域。IFN基因缺失患者的正常细胞具有α、β和ω干扰素基因的两个等位基因。在所有患者的细胞中均未检测到γ干扰素基因的缺失或重排。我们得出结论,在11例急性淋巴细胞白血病患者中有2例,其恶性转化伴随着9号染色体一条或两条上的物质缺失,且α、β和ω干扰素基因包含在这些缺失中。