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      Identification of cDNAs induced by the tumor suppressor Tsc2 gene using a conditional expression system in Tsc2 mutant (Eker) rat renal carcinoma cells.

      Biochemical and Biophysical Research Communications
      Animals, Apoptosis, genetics, Cell Cycle, physiology, Cloning, Molecular, Gene Expression Regulation, Neoplastic, Genes, Tumor Suppressor, Humans, Kidney Neoplasms, metabolism, Kinetics, RNA, Messenger, Rats, Repressor Proteins, Sequence Analysis, DNA, Signal Transduction, Stress, Physiological, Tuberous Sclerosis, Tumor Cells, Cultured, Tumor Suppressor Proteins

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          Abstract

          Alteration of the rat homologue of the tuberous sclerosis 2 (TSC2) gene is associated with dominantly inherited cancer in the Eker rat model, indicating a tumor suppressor nature. The ability of Tsc2 to activate signal transduction and transcription suggests that genes induced by Tsc2 may mediate its biological roles. Using a subtractive hybridization approach in combination with tetracycline operator systems, we identified a set of downstream genes affected by Tsc2. Regulated expression of wild-type Tsc2 gene in Eker renal carcinomas (RCs) resulted in marked expression of cell arrest or programmed cell-death-related genes and stress-induced genes. Thus, the data suggest that Tsc2 might contribute to regulation of the cell cycle and cell survival.

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