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PMID: 8298644 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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

Nature genetics ·Vol. 5 ·No. 4 ·1993-12-00 ·Pages 363-7

Park S, Bernard A, Bove KE, Sens DA, Hazen-Martin DJ, Garvin AJ, Haber DA

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.

MeSH Terms
Amino Acid Sequence Child Child, Preschool Chromosomes, Human, Pair 13 DNA Mutational Analysis Female Genes, Wilms Tumor Humans Infant Kidney/pathology Kidney Neoplasms/genetics,pathology Molecular Sequence Data Mutation Polymorphism, Genetic Wilms Tumor/genetics,pathology
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Park S
Laboratory of Molecular Genetics, Massachusetts General Hospital Cancer Center, Charlestown.
Bernard A
Bove K E
Sens D A
Hazen-Martin D J
Garvin A J
Haber D A
Article Info
Journal
Nature genetics
Abbr.
Nat Genet
ISSN
1061-4036
Published
1993-12-00
Pages
363-7
Language
English
Region
United States
NLM ID
9216904
Subset
IM
Grants
NCI NIH HHS · CA37887 · United States
NCI NIH HHS · CA58596 · United States
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