Multiple roles for the Wilms' tumour suppressor gene, WT1 genitourinary development

被引：26

作者：

Schedl, A

Hastie, N

机构：

[1] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland

[2] Max Delbruck Ctr Mol Med, D-13122 Berlin, Germany

来源：

MOLECULAR AND CELLULAR ENDOCRINOLOGY | 1998年 / 140卷 / 1-2期

关键词：

Wilms' tumour; WAGR syndrome; genitourinary development;

D O I：

10.1016/S0303-7207(98)00031-8

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Wilms' tumour is a childhood kidney cancer, and a classic example of cancer arising through disrupted development (Armstrong et al., 1992). It is one of the most common solid paediatric malignancies, affecting one in 10 000 children. The genetics of Wilms' tumour is complicated, with several different genes or chromosomal regions being implicated (Armstrong el al., 1992). However, the gene we know most about is the Wilms' tumour predisposition gene, WT1 (Bickmore et al., 1992; Bruening and Pelletier, 1996). It is now clear that mutations in this gene in humans can lead to abnormalities of the kidneys and gonads, as well as to the eponymous tumour. Also, as discussed below, WT1 is essential for kidney, testis and ovary development, as revealed in knockout mice. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.

引用

页码：65 / 69

页数：5

共 35 条

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