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Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour

Nature Genetics volume 5, pages 363–367 (1993)Cite this article

Abstract

Nephrogenic rests consist of foci of primitive renal cells, typically microscopic, that are found within the normal kidney tissue of children with Wilms' tumour. To study the relationship between nephrogenic rests and the associated tumours, we screened these lesions for mutations in the 11p13 Wilms' tumour suppressor gene, WT1. In two cases in which the Wilms' tumour contained a somatic WT1 mutation, the nephrogenic rest had the identical mutation. Nephrogenic rests and Wilms' tumours are therefore topographically distinct lesions that are clonally derived from an early renal stem cell. Inactivation of WT1 appears to be an early genetic event which can lead to the formation of nephrogenic rests, enhancing the probability that additional genetic hits will lead to Wilms' tumour.

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Authors and Affiliations

  1. Laboratory of Molecular Genetics, Massachusetts General Hospital Cancer Center and Harvard Medical School, Charlestown, Massachusetts, 02129, USA

    Seon Park, Amy Bernard & Daniel A. Haber

  2. Deparment of Pathology, Children's Hospital Medical Center, Cincinnati, Ohio, 45229, USA

    Kevin E. Bove

  3. Department of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, South Carolina, 29425, USA

    Donald A. Sens, Debra J. Hazen-Martin & A. Julian Garvin

Authors
  1. Seon Park
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  2. Amy Bernard
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  3. Kevin E. Bove
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  4. Donald A. Sens
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  6. A. Julian Garvin
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  7. Daniel A. Haber
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Park, S., Bernard, A., Bove, K. et al. Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour. Nat Genet 5, 363–367 (1993). https://doi.org/10.1038/ng1293-363

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