The patterns of RET proto-oncogene expression in mouse, rat, and chicken and the anomalies observed in targeted RET mutants suggest that RET plays a major role in development of mouse enteric nervous system and in kidney organogenesis. Here, we report on in situ hybridization studies describing the
PROTO-ONCOGENE EXPRESSION IN HUMAN GLOMERULAR DISEASES
β Scribed by TAKEMURA, TSUKASA; OKADA, MITSURU; AKANO, NORIHISA; MURAKAMI, KATSUMI; HINO, SATOSHI; YAGI, KAZURO; TAKEKOSHI, YASUO; YOSHIOKA, KAZUO
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 863 KB
- Volume
- 178
- Category
- Article
- ISSN
- 0022-3417
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β¦ Synopsis
The expression of the protein products and mRNA of c-fos, c-myc, p53, and c-rafwas examined in normal renal tissues and biopsy specimens from 73 patients with various glomerular diseases. Immunofluorescent staining showed that there were cell nuclei stained for C-FOS, c-Myc, and p53, and cytoplasm positive for c-Raf, in the glomeruli of patients with proliferative types of glomerulonephritis, including IgA nephritis and lupus nephritis, and in patients with focal glomerular sclerosis. Glomerular expression of c-fos and c-myc mRNA was detected by in situ hybridization. The number of proto-oncogene-positive glomerular cells was significantly higher in lupus nephritis, IgA nephritis, and focal segmental sclerosis, as compared with minimal change nephrotic syndrome and normal specimens. In IgA nephritis, the population of glomerular cells positive for c-Fos and c-Myc and the grade of c-Raf immunoreactivity were significantly correlated with the proportion of proliferating cell nuclear antigen (PCNA)-positive glomerular cells, with histological grading of mesangial hypercellularity and matrix increase, and with the magnitude of proteinuria. These data indicate that proto-oncogene expression is associated with mesangial proliferation and matrix expansion in proliferative types of glomerulonephritis and in focal glomerular sclerosis.
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