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EXPRESSION OF THE PAX2 GENE IN HUMAN FETAL KIDNEY AND WILMS-TUMOR
Author(s): ECCLES MR, WALLIS LJ, FIDLER AE, SPURR NK, GOODFELLOW PJ, REEVE AE
Source: CELL GROWTH & DIFFERENTIATION    Volume: 3    Issue: 5    Pages: 279-289    Published: MAY 1992  
Times Cited: 102     References: 53     
Abstract: We have examined the pattern of expression of the human PAX2 gene in Wilms' tumors and human fetal kidney by Northern blot and in situ hybridization. Human PAX2 encodes a paired box-containing protein and has a high degree of homology with mouse and Drosophila paired box genes. In situ hybridization analysis reveals that PAX2 is expressed in nephrogenic structures in fetal kidney and also in Wilms' tumors. This pattern of expression suggests that PAX2 may have a role in differentiation of tissues in the kidney. In fetal kidney, PAX2 expression rapidly attenuates following the initial differentiation, but no evidence of attenuation was found in Wilms' tumors. The timing of PAX2 expression is restricted to fetal development, although high levels of expression were also observed in nephrogenic rests of residual normal juvenile kidney tissue adjacent to a Wilms' tumor. Nephrogenic rests are the presumptive precursors of Wilms' tumor but are not necessarily neoplastic. The failure of PAX2 expression to attenuate in Wilms' tumors and nephrogenic rests may be associated with events leading to the onset of Wilms' tumor. By somatic cell hybrid mapping, the PAX2 gene was localized to chromosome 10q22.1-q24.3, although this region has not previously been implicated in Wilms' tumor.
Document Type: Article
Language: English
Reprint Address: ECCLES, MR (reprint author), UNIV OTAGO, CTR GENE RES, DEPT BIOCHEM, MOLEC CARCINOGENESIS LAB, POB 56, DUNEDIN, NEW ZEALAND
Addresses:
1. IMPERIAL CANC RES FUND, CLARE HALL LABS, HERTFORD EN6 3LD, ENGLAND
2. UNIV BRITISH COLUMBIA, DEPT MED GENET, VANCOUVER V6T 1W5, BC CANADA
Publisher: AMER ASSOC CANCER RESEARCH, PUBLIC LEDGER BLDG, SUITE 816, 150 S. INDEPENDENCE MALL W., PHILADELPHIA, PA 19106
Subject Category: Cell Biology
IDS Number: HU319
ISSN: 1044-9523
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