Author/Authors :
Pola?ski، نويسنده , , Rados?aw and Noon، نويسنده , , Aidan P. and Blaydes، نويسنده , , Jeremy C. Phillips، نويسنده , , Anna and Rubbi، نويسنده , , Carlos P. and Parsons، نويسنده , , Keith and Vlatkovi?، نويسنده , , Nikolina and Boyd، نويسنده , , Mark T.، نويسنده ,
Abstract :
Although the role of p53 as a tumour suppressor in renal cell carcinoma (RCC) is unclear, our recent analysis suggests that increased wild-type p53 protein expression is associated with poor outcome. A growing body of evidence also suggests that p53 expression and increased co-expression of MDM2 are linked with poor prognosis in RCC. We have therefore examined whether an MDM2 antagonist; Nutlin-3, might rescue/increase p53 expression and induce growth inhibition or apoptosis in RCC cells that retain wild-type p53. We show that inhibition of p53 suppression by MDM2 in RCC cells promotes growth arrest and p53-dependent senescence – phenotypes known to mediate p53 tumour suppression in vivo. We propose that future investigations of therapeutic strategies for RCC should incorporate MDM2 antagonism as part of strategies aimed at rescuing/augmenting p53 tumour suppressor function.
Keywords :
senescence , renal cell carcinoma , p53 , Nutlin-3 , MDM2 , Targeted therapy