Tissue, Developmental, and Tumor-Specific Expression of Divergent Transcripts in Wilms Tumor

Annie Huang(University of Toronto), Christine Campbell(University of Toronto), Laura Bonetta(University of Toronto), Monica McAndrews-Hill(Hospital for Sick Children), Susan Chilton‐MacNeill(Hospital for Sick Children), Max J. Coppes(Hospital for Sick Children), David Law(University of Michigan), Andrew P. Feinberg(University of Michigan), Herman Yeger(Hospital for Sick Children), Bryan Williams(University of Toronto)
Science
November 16, 1990
Cited by 163

Abstract

The Wilms tumor locus on chromosome 11p13 has been mapped to a region defined by overlapping, tumor-specific deletions. Complementary DNA clones representing transcripts of 2.5 (WIT-1) and 3.5 kb (WIT-2) mapping to this region were isolated from a kidney complementary DNA library. Expression of WIT-1 and WIT-2 was restricted to kidney and spleen. RNase protection revealed divergent transcription of WIT-1 and WIT-2, originating from a DNA region of less than 600 bp. Both transcripts were present at high concentrations in fetal kidney and at much reduced amounts in 5-year-old and adult kidneys. Eleven of 12 Wilms tumors classified as histopathologically heterogeneous exhibited absent or reduced expression of WIT-2, whereas only 4 of 14 histopathologically homogeneous tumors showed reduced expression. These data demonstrate a molecular basis for the pathogenetic heterogeneity in Wilms tumorigenesis.


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