Renal carcinogenesis in the Eker rat
Autor: | O. Hino, E. Kobayashi, M. Nishizawa, Y. Kubo, T. Kobayashi, Y. Hirayama, S. Takai, Y. Kikuchi, H. Tsuchiya, K. Orimoto, K. Kajino, T. Takahara |
---|---|
Rok vydání: | 1995 |
Předmět: |
Male
Cancer Research DNA Complementary Tumor suppressor gene Molecular Sequence Data Biology medicine.disease_cause Rats Mutant Strains Gene product Tuberous Sclerosis medicine Animals Humans RNA Messenger RNA Neoplasm Gene Annexin A2 DNA Primers Genes Dominant Regulation of gene expression Kidney Base Sequence General Medicine Kidney Neoplasms Rats Gene Expression Regulation Neoplastic medicine.anatomical_structure Oncology Mesothelin Cancer research Representational difference analysis TSC2 Carcinogenesis Proto-Oncogene Proteins c-fos Chromosomes Human Pair 16 |
Zdroj: | Journal of Cancer Research and Clinical Oncology. 121:602-605 |
ISSN: | 1432-1335 0171-5216 |
DOI: | 10.1007/bf01197777 |
Popis: | The Eker rat hereditary renal carcinoma is an excellent example of a Mendelian dominant predisposition to a specific cancer in an experimental animal. We recently reported that a germline insertion in the rat homologue of the human tuberous sclerosis (TSC2) gene gives rise to the dominantly inherited cancer in the Eker rat model. The function of the TSC2/Tsc2 gene product (called "tuberine" in the human case) is not yet understood, although it contains a short amino acid sequence homologous to the ras family GTPase-activating proteins (GAP3). In the study, we isolated subtracted cDNA clones having increased expression in Eker renal carcinoma cells, using a modified representational difference analysis method to search for additional genes specifically involved in renal carcinogenesis. Here we identified four genes: the third component of the complement (C3) gene, the fos-related antigen I (fra-1) gene, an unknown gene (designated as being expressed in renal carcinoma: erc) and the calpactine I heavy-chain (Annexin II) gene. |
Databáze: | OpenAIRE |
Externí odkaz: |