Inactivation of tumour suppressor gene(s) (TSGs) on 3p appears to be a critical event in the pathogenesis of clear cell renal cell carcinoma (CC-RCC). Analysis of loss of heterozygosity (LOH) in sporadic RCC samples has implicated roles for TSGs in three specific regions of 3p in RCC development: (1
Loss of heterozygosity studies indicate that chromosome arm 1p harbors a tumor suppressor gene for renal oncocytomas
✍ Scribed by Catherine A. Thrash-Bingham; Hernando Salazar; Richard E. Greenberg; Kenneth D. Tartof
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 387 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1045-2257
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✦ Synopsis
We carried out a complete genome scan for loss of heterozygosity (LOH) in four renal oncocytomas by using highly polymorphic CA repeat microsatellite loci. Three of the four tumors exhibited LOH for chromosome arm I p, and the oncocytomas of both female patients lost Xq. Therefore, these chromosome arms may harbor tumor suppressor genes involved in the etiology of this disease. Although the genomes of oncocytomas are relatively stable, two different microsatellite loci in one tumor were mutated by ? 2 nt. Similar alterations in CA repeats that are probably due to spontaneous mutation have been observed in renal cell carcinomas.
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