The long-term goal of this proposal is to understand the normal biological function of the hMDM2 oncoprotein and how its overexpression can induce tumorigenesis. The short-term objective is to test the hypothesis that hMDM2 induces cell cycle arrest, possibly by interacting with the cell cycle regulatory proteins. Inactivation of this function is one of the causes of tumorigenesis. The working hypotheses are based on the exciting observations that mMDM2 induces GO/G1 arrest in normal human diploid cells. Elimination of the growth arrest function enhances the tumorigenic potential of NIH3T3 cells. Furthermore, hMDM2 associates with two cell cycle regulatory proteins, cyclin E and p34 (cdc2). This proposal has four specific aims. 1) Consequence of hMDM2 overexpression in normal breast epithelial cells and breast tumor- derived cells will be analyzed. The domain(s) of hMDM2 needed to confer these growth alterations will be determined using deletion mutants of the oncoprotein. Identification of these domains will enable us to detect interactions of hMDM2 with other proteins (such as cyclin E) important for cellular growth regulator functions. 2) Different splice variants of mdm2 mRNA will be isolated from an hMDM2 overexpressing breast cancer cell line MCF-7 and a murine tumorigenic cell line 3T3DM (harbors amplified mdm2 gene). The growth regulatory properties of the proteins encoded by the different splice variants will be analyzed. 3) The consequence of hMDM2-cyclin E interaction on the cyclin E-associated kinase -activity and on cell growth will be determined. 4) Since hMDM2 associates with P34 (cdc2), how hMDM2 modulates the activation of p34 (cdc2) kinase activity and how this interaction modulates cell growth will be determined. Completion of these specific aims will elucidate a novel growth regulatory function of hMDM2 and how perturbation of that function leads to tumorigenesis.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA074172-04
Application #
6376402
Study Section
Metabolic Pathology Study Section (MEP)
Project Start
1998-09-20
Project End
2004-06-30
Budget Start
2001-07-01
Budget End
2004-06-30
Support Year
4
Fiscal Year
2001
Total Cost
$229,081
Indirect Cost
Name
Virginia Commonwealth University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
Ramamoorthy, Mahesh; Vaughan, Catherine; Deb, Sumitra et al. (2013) Measurement of chemosensitivity and growth rate in p53 expressing cells. Methods Mol Biol 962:127-33
Vaughan, Catherine; Deb, Swati Palit; Deb, Sumitra (2013) Generation of p53 knock-down cell lines. Methods Mol Biol 962:193-9
Vaughan, Catherine A; Singh, Shilpa; Windle, Brad et al. (2012) p53 mutants induce transcription of NF-?B2 in H1299 cells through CBP and STAT binding on the NF-?B2 promoter and gain of function activity. Arch Biochem Biophys 518:79-88
Vaughan, Catherine A; Frum, Rebecca; Pearsall, Isabella et al. (2012) Allele specific gain-of-function activity of p53 mutants in lung cancer cells. Biochem Biophys Res Commun 428:6-10
Frum, Rebecca; Ramamoorthy, Mahesh; Mohanraj, Lathika et al. (2009) MDM2 controls the timely expression of cyclin A to regulate the cell cycle. Mol Cancer Res 7:1253-67
Scian, M J; Carchman, E H; Mohanraj, L et al. (2008) Wild-type p53 and p73 negatively regulate expression of proliferation related genes. Oncogene 27:2583-93
Frum, Rebecca; Busby, Scott A; Ramamoorthy, Mahesh et al. (2007) HDM2-binding partners: interaction with translation elongation factor EF1alpha. J Proteome Res 6:1410-7
Scian, Mariano J; Stagliano, Katherine E R; Anderson, Michelle A E et al. (2005) Tumor-derived p53 mutants induce NF-kappaB2 gene expression. Mol Cell Biol 25:10097-110
Zhou, Ruizhe; Frum, Rebecca; Deb, Sumitra et al. (2005) The growth arrest function of the human oncoprotein mouse double minute-2 is disabled by downstream mutation in cancer cells. Cancer Res 65:1839-48
Scian, Mariano J; Stagliano, Katherine E R; Ellis, Michelle A et al. (2004) Modulation of gene expression by tumor-derived p53 mutants. Cancer Res 64:7447-54

Showing the most recent 10 out of 20 publications