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Abstract
Grant Number: 5R37CA055360-12 Project Title: MECHANISMS OF SIGNAL TRANSDUCTION BY RAS PROTEINS
PI Information: Name Title BAR-SAGI, DAFNA barsad01@nyumc.org PROFESSOR AND CHAIR Abstract: Cancer is a disease in which growth stimulatory pathways are excessively active. Considerable experimental evidence implicates Ras proteins as essential components of growth stimulatory signal transduction pathways and mutated Ras proteins as important contributors to human carcinogenesis. The broad objective of this research project is to define the molecular mechanisms underlying the growth promoting activity of Ras. The combined efforts of many groups, including our own, have led to the realization that the biological effects of Ras are mediated by a network of interconnecting pathways. However, the distinct contribution of these pathways to the mitogenic and oncogenic effects of Ras has remained poorly defined. During the past grant period, we have identified effector pathways that mediate the proliferative and cell survival responses to Ras. The goal of the studies proposed in the current application is to define the mechanisms by which these effector pathways contribute to both normal and deregulated cell growth. Our specific aims are as follows: 1. To define the mechanisms by which Rac contributes to Ras-induced cell cycle progression. 2. To identify Rac-dependent effector activities that mediate the mitogenic response. 3. To establish the role of Ras-dependent cell survival signals in oncogenic transformation. 4. To identify the signaling activities of Ras involved in pancreatic cancer. Together, the experiments proposed herein should serve the dual purpose of advancing our understanding of growth control in normal cells and providing insights into how the regulation of cell growth is disturbed in cancer cells.
Public Health Relevance:
This Public Health Relevance is not available.Thesaurus Terms:
biological signal transduction, cell growth regulation, guanine nucleotide binding protein, neoplastic transformation, pancreas neoplasm
enzyme activity, oligonucleotide, oncogene, phosphorylation, protein kinase
laboratory rat, tissue /cell culture
Institution: STATE UNIVERSITY NEW YORK STONY BROOK The Office of Sponsered Programs STONY BROOK, NY 11794 Fiscal Year: 2002 Department: MOLECULAR GENETICS AND MICROBIOLOGY Project Start: 01-JUL-1991 Project End: 30-APR-2006 ICD: NATIONAL CANCER INSTITUTE IRG: CDF