The long-term objective of our ongoing, multi-project research program is to understand molecular mechanisms for cellular regulation by signal transduction. Most of our project focus on cellular transducers that have oncogenic potential in the absence of regulation. We think that many oncogenes are likely to interact in common signal transduction pathways designed for regulation of cellular proliferation. Our projects include study of growth factor receptors at the cell surface, signal transduction networks in the cytoplasm, and transcription factors operating in the nucleus. Our research projects are: 1: Regulation of mammalian Ras exchange factor Sos 2: Regulation of hematopoiesis by epidermal growth factor receptor 3: Regulation of transcription factor E2F 4: Regulation of gene expression by prolactin 5: Regulation of cellular proliferation by p53 Our program project grant includes five investigators at the State university of new York at Stony Brook. Our interdisciplinary approaches include cell biology, molecular biology, genetics, and structure. During the past 15 years, our program has evolved from a study of tumor-virus- associated oncogenes to our present emphasis on signal transduction.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA028146-17
Application #
2414096
Study Section
Cancer Centers and Research Programs Review Committee (CCRP)
Project Start
1980-08-01
Project End
2001-04-30
Budget Start
1997-05-09
Budget End
1998-04-30
Support Year
17
Fiscal Year
1997
Total Cost
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
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
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
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

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