Combined Vhl, Trp53 and Rb1 mutation causes clear cell renal cell carcinoma in mice
[Paper-level Aggregated] PMCID: PMC5509015
Evidence Type(s): Oncogenic, Functional, Predisposing
Justification: Oncogenic: The deletion of Trp53 in combination with Vhl and Rb1 significantly accelerates tumor formation in mice, indicating that these genetic alterations contribute to oncogenesis in the context of ccRCC. Functional: The study demonstrates that the genetic deletions and mutations lead to functional changes in renal epithelial cells, such as the loss of pRB immunoreactivity and the accumulation of HIF-1alpha, which are indicative of altered cellular functions associated with tumorigenesis. Predisposing: The presence of specific genetic deletions (Vhl, Trp53, Rb1) in mice predisposes them to develop ccRCC, as evidenced by the increased incidence and earlier onset of tumors in genetically modified mice compared to controls.
Gene→Variant (gene-first): VHL(7428):A>G VHL(7428):C>A VHL(7428):C>T VHL(7428):G>A VHL(7428):G>T VHL(7428):T>C VHL(7428):Trp53 deletion
Genes: VHL(7428)
Variants: A>G C>A C>T G>A G>T T>C Trp53 deletion