The microenvironment in which cancer develops is crucial both to basic cancer biology and the development of novel therapeutic concepts. Effective in vivo models in whole animals are needed to address these issues and to assess adverse side effects of cancer therapies including radiation. In preliminary work it was stablished that zebrafish embryos provide a facile system to assess modulation of the radiation response in vivo. The applicant will extend these studies to critically examine the functional contribution of distinct p53 Family members to the radiation response in normal tissues and organs. This work will be performed by using state-of-the-art methods of downregulating gene expression or function and has important translational ramifications.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31CA119951-04
Application #
7491214
Study Section
Special Emphasis Panel (ZRG1-ONC-P (29))
Program Officer
Bini, Alessandra M
Project Start
2005-09-12
Project End
2009-09-11
Budget Start
2008-09-12
Budget End
2009-09-11
Support Year
4
Fiscal Year
2008
Total Cost
$39,373
Indirect Cost
Name
Thomas Jefferson University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
053284659
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
Davidson, William R; Kari, Csaba; Ren, Qing et al. (2010) Differential regulation of p53 function by the N-terminal ?Np53 and ?113p53 isoforms in zebrafish embryos. BMC Dev Biol 10:102
Davidson, William; Ren, Qing; Kari, Gabor et al. (2008) Inhibition of p73 function by Pifithrin-alpha as revealed by studies in zebrafish embryos. Cell Cycle 7:1224-30