The Ras oncogene mediates a variety of biological effects which promote tumorigenic transformation. However, activated forms of Ras also have a surprising number anti-transformation aspects. They can induce senesence, cell cycle arrest and even death by apoptosis. The mechanisms behind these anti-neolastic effects remain poorly understood. We have identified a famiuly of novel Ras effectors which appear to mediate some of the anti-neoplastic activities of Ras. especialy apoptosis. At least one of these genes is frequently deranged during the development of human cancers and so this group of Ras effectors may be a family of Ras regulated tumor suppressors.

Agency
National Institute of Health (NIH)
Institute
Division of Clinical Sciences - NCI (NCI)
Type
Intramural Research (Z01)
Project #
1Z01SC010359-02
Application #
6558774
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Clinical Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Ahmed-Choudhury, Jalal; Agathanggelou, Angelo; Fenton, Sarah L et al. (2005) Transcriptional regulation of cyclin A2 by RASSF1A through the enhanced binding of p120E4F to the cyclin A2 promoter. Cancer Res 65:2690-7
Elam, Candice; Hesson, Luke; Vos, Michele D et al. (2005) RRP22 is a farnesylated, nucleolar, Ras-related protein with tumor suppressor potential. Cancer Res 65:3117-25
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