Hartley A L, Birch J M, Harris M, Blair V, Morris Jones P H, Gattamaneni H R, Kelsey A M
CRC Paediatric and Familial Cancer Research Group, Christie Hospital NHS Trust, Manchester, England.
Cancer Genet Cytogenet. 1994 Oct 15;77(2):129-33. doi: 10.1016/0165-4608(94)90228-3.
Leukemias and lymphomas occurring in a series of families with Wilms' tumor (WT) are described. One surviving case developed a large cell anaplastic Ki-1 lymphoma at age 20 years, and 23 second- and higher degree relatives were affected. In two instances leukemia/lymphoma occurred in the context of Li-Fraumeni syndrome (LFS) and two other families showed striking clusters of unusual and early-onset malignancies. In several cases, children had genitourinary abnormalities of the type associated with the WT1 gene on chromosome 11p13. Some of these families may provide important subjects for study of WT genes in hematologic disease and lymphomas and for investigation of interaction between different tumor-suppressor genes, e.g., WT1 and other candidate WT genes, and p53.
本文描述了一系列患有威尔姆斯瘤(WT)的家族中发生的白血病和淋巴瘤。一名存活病例在20岁时患了大细胞间变性Ki-1淋巴瘤,并且23名二级及以上亲属也受到影响。在两例中,白血病/淋巴瘤发生在李-弗劳梅尼综合征(LFS)背景下,另外两个家族显示出不寻常的早发恶性肿瘤的显著聚集。在几例病例中,儿童存在与11号染色体p13上WT1基因相关类型的泌尿生殖系统异常。这些家族中的一些可能为研究血液系统疾病和淋巴瘤中的WT基因以及不同肿瘤抑制基因(如WT1和其他候选WT基因以及p53)之间的相互作用提供重要研究对象。