In preliminary work, the investigator has identified a novel receptor-ligand interaction between the cytokine, osteopontin, and the homing receptor, CD44. Both receptor and ligand are typically expressed by activated lymphocytes, and may play important roles in lymphocyte homing. In addition, osteopontin and CD44 expression are associated with tumor cells, and may play important roles in the directed metastatic spread of specific tumor types. This project will investigate in detail the roles of variable RNA splicing and protein glycosylation in the functions of CD44 and osteopontin. The investigator will define post-receptor signaling events initiated by the binding of osteopontin to CD44, and will attempt to correlate these events with the cellular responses of apoptosis and migration. Transfection and antisense technologies will be used to define the contributions of the osteopontin-CD44 system to tumor growth and spread in vivo. These studies could provide important insights into the mechanism of tumor metastasis.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
7R29CA076176-03
Application #
6124708
Study Section
Experimental Immunology Study Section (EI)
Program Officer
Ault, Grace S
Project Start
1997-12-05
Project End
2002-11-30
Budget Start
2000-01-01
Budget End
2000-11-30
Support Year
3
Fiscal Year
2000
Total Cost
$110,485
Indirect Cost
Name
Tufts University
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02111