One of the most effected genes in the human tumors is p53. About 60% of human cancers contain mutation in p53 gene. Although the regulation of p53 is well studied, very little is known about the regulation of mutant p53. We have shown previously that a human B-lymphoma cell line (RL) harboring mutant p53, which is refractory to the growth inhibitory effects of transforming growth factor-beta(TGF-beta),can be rendered sensitive to TGF- beta by induction of receptors for TGF-beta with low concentrations of phorbol myristate acetate (PMA). We have also shown the growth inhibitory effect of TGF-beta was associated with a down regulation of mutant p53. To know the regulation of mutant p53, we are examining the signal transduction molecules involved in the down regulation of mutant p53 by TGF-beta. We are also examining the effect of PFT-a, a newly discovered inhibitor of p53 signaling, on the mutant p53 and the growth of RL cells.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Intramural Research (Z01)
Project #
1Z01AG000116-02
Application #
6521712
Study Section
(LI)
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Aging
Department
Type
DUNS #
City
State
Country
United States
Zip Code
O'Farrell, Thomas J; Ghosh, Paritosh; Dobashi, Nobuaki et al. (2004) Comparison of the effect of mutant and wild-type p53 on global gene expression. Cancer Res 64:8199-207