The development of cancer is a multistep process involving multiple genetic changes that lead to the malignant state. These genetic changes occur in molecules involved in the most basic decisions that a cell must make, namely proliferation, differentiation and cell death. In order to understand cancer more fully, it is important to analyze how these molecules function in normal cells and how their functions are perturbed in cancer. The central theme of this program is the analysis of signaling pathways that control cellular growth, differentiation, and cell survival, and how these signals are directed from the cytoplasm to the nucleus where transcriptional changes enact growth regulatory signals. The goal of the program is to understand the molecular mechanisms of specificity that direct proliferative signals from the cell surface, through the cytoplasm, and into the nucleus. Our Program consists of vie investigators in the School of Medicine at the State University of New York at Stony Book whose research focuses on signal transduction and gene regulation. During the past twenty years, our Program has evolved from a study of tumor virus-associated oncogenes to our present emphasis on signal transduction and the regulation of cell growth. The research projects described in the proposal are: Project 1: Positive and Negative Regulation of RTK-Ras Signaling Project 2: Role of Growth Factor Receptors in Hematopoietic Malignancies Project 3: Regulation of Transcription Factor E2F Project 4: Determinants of Tyrosine Kinase Specificity Project 5: Cytokine Signaling to the Nucleus Core 1: Administration Core 2: Sequencing Core 3: Protein Expression

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA028146-23
Application #
6605686
Study Section
Subcommittee G - Education (NCI)
Program Officer
Wong, May
Project Start
1980-08-01
Project End
2006-06-30
Budget Start
2003-07-03
Budget End
2004-06-30
Support Year
23
Fiscal Year
2003
Total Cost
$1,680,858
Indirect Cost
Name
State University New York Stony Brook
Department
Genetics
Type
Schools of Medicine
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
Feres, Kimberly J; Hayman, Michael J (2010) RON-expressing MCF-10A breast epithelial cells exhibit alterations of hyaluronan expression, promoting RON-mediated early adhesion events. Biochem Biophys Res Commun 391:1604-9
Feres, K J; Ischenko, I; Hayman, M J (2009) The RON receptor tyrosine kinase promotes MSP-independent cell spreading and survival in breast epithelial cells. Oncogene 28:279-88
Yoo, Jae Cheal; Hayman, Michael J (2007) Annexin II binds to SHP2 and this interaction is regulated by HSP70 levels. Biochem Biophys Res Commun 356:906-11
Tartaglia, Marco; Pennacchio, Len A; Zhao, Chen et al. (2007) Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. Nat Genet 39:75-9
Reich, Nancy C (2007) STAT dynamics. Cytokine Growth Factor Rev 18:511-8
Yondola, Mark A; Hearing, Patrick (2007) The adenovirus E4 ORF3 protein binds and reorganizes the TRIM family member transcriptional intermediary factor 1 alpha. J Virol 81:4264-71
Ullman, Amanda J; Reich, Nancy C; Hearing, Patrick (2007) Adenovirus E4 ORF3 protein inhibits the interferon-mediated antiviral response. J Virol 81:4744-52
Zhao, Chen; Du, Guangwei; Skowronek, Karl et al. (2007) Phospholipase D2-generated phosphatidic acid couples EGFR stimulation to Ras activation by Sos. Nat Cell Biol 9:706-12
Kim, Hong Joo; Taylor, Laura J; Bar-Sagi, Dafna (2007) Spatial regulation of EGFR signaling by Sprouty2. Curr Biol 17:455-61
Merritt, Rebecca; Hayman, Michael J; Agazie, Yehenew M (2006) Mutation of Thr466 in SHP2 abolishes its phosphatase activity, but provides a new substrate-trapping mutant. Biochim Biophys Acta 1763:45-56

Showing the most recent 10 out of 281 publications