Miyagi T, Ahuja H, Kubota T, Kubonishi I, Koeffler H P, Miyoshi I
Department of Medicine, Kochi Medical School, Japan.
Leukemia. 1993 Jul;7(7):970-7.
Wilms' tumor (WT) is a pediatric malignancy that occurs in embryonic kidney. Recently, a putative Wilms' tumor gene (WT1), located on chromosome 11p13, was isolated and characterized. We found constitutive expression of WT1 mRNA in eight out of 22 hematopoietic cell lines and seven out of 26 clinical samples which were derived from patients with various types of hematologic malignancies. WT1 mRNA was detected in four out of six myeloid cell lines, four out of 10 cases of acute myelocytic leukemia, three out of 15 lymphoid cell lines, one out of nine cases of lymphoid malignancies, and one out of six cases of chronic myelocytic leukemia in accelerated phase and blast crisis. One unclassified hematopoietic cell line and a case of myelodysplastic syndrome also expressed WT1 mRNA. No mutations were detectable in the cell lines by Southern blot analysis and a polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) analysis in the four zinc finger domains of the WT1 gene. These results suggest that WT1 gene is expressed in several types of immature lymphoid or myeloid leukemia cells possibly without alterations of the WT1 gene.
肾母细胞瘤(WT)是一种发生于胚胎肾的儿童恶性肿瘤。最近,位于11号染色体p13区域的一个假定的肾母细胞瘤基因(WT1)被分离并鉴定。我们发现,在22种造血细胞系中有8种以及在26份来自各类血液系统恶性肿瘤患者的临床样本中有7份存在WT1 mRNA的组成型表达。在6种髓系细胞系中有4种、10例急性髓细胞白血病中有4例、15种淋巴系细胞系中有3种、9例淋巴系恶性肿瘤中有1例以及6例加速期和急变期慢性髓细胞白血病中有1例检测到WT1 mRNA。一种未分类的造血细胞系和1例骨髓增生异常综合征也表达WT1 mRNA。通过Southern印迹分析以及WT1基因4个锌指结构域的聚合酶链反应-单链构象多态性(PCR-SSCP)分析,未在细胞系中检测到突变。这些结果表明,WT1基因在几种类型的未成熟淋巴系或髓系白血病细胞中表达,可能不存在WT1基因的改变。