Ras and Ras-related (Rabs) proteins have been shown to play critical roles in human oncogeneis, controlling normal cell proliferation, inducing differentiated phenotypes and regulating membrane traffic. Over the past few years it has become apparent that many types of signals arriving at the cell surface activate Ras, and that active Ras and Rabs can stimulate multiple downstream targets. The major goal of future research will be to understand how Ras uses these multiple signaling cascades to mediate such diverse effects in cells. Rho family GTPases have also been shown to activate multiple downstream targets that ultimately lead to alterations in the actin cytoskeleton and gene transcription. Activation of Rho family members has also been shown recently to be an important component of Ras mediated cell transformation. Future goals in this area include elucidating the molecular details of how Rho proteins carry out their functions through multiple effector proteins, and how Rho family proteins are activated by upstream signals.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Conference (R13)
Project #
1R13CA080133-01
Application #
2745275
Study Section
Special Emphasis Panel (SRC (O1))
Program Officer
Spalholz, Barbara A
Project Start
1999-03-01
Project End
2000-02-29
Budget Start
1999-03-01
Budget End
2000-02-29
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Keystone Symposia
Department
Type
DUNS #
079780750
City
Silverthorne
State
CO
Country
United States
Zip Code
80498
Sclafani, Anthony; Chen, Shuliang; Rivera-Molina, Felix et al. (2010) Establishing a role for the GTPase Ypt1p at the late Golgi. Traffic 11:520-32