The objective of this Program Project is to unite a network of scientific investigators who are focusing on the molecular biology of the cell cycle in order to understand the mechanisms of oral carcinogenesis. This proposal consists of six highly interdependent research projects and cores, connected both scientifically and technically. The central theme uniting the three research projects is the perturbation of key cell cycle regulators in the genesis of oral cancer. These key regulators as well as a novel cell cycle regulator have been identified by this research group. Findings from the research projects will be validated by collaborative efforts of the Cell Culture Core and the Tissue Bank and Pathology Core. This program project will support and promote synergistic interactions among the cores and research projects that will speed up the investigations of the process central to the development of oral cancer: cell cycle control. There are three research projects in this oral cancer program project: """"""""HPV and Cell Cycle Dysregulation in Oral Cancer"""""""" will study the role of human papillomavirus (HPV), the p53 and pRB pathways, and the cell cycle regulator cdk6 in oral cancer. """"""""Cyclin D1 and a Genetic Model of Oral Carcinogenesis"""""""" will investigate the genetic basis of proliferation and transformation of oral keratinocytes by the aberrant expression of the G1- specific cyclin D1 oncogene in a transgenic mouse model. """"""""Cell cycle Biology of doc-1"""""""" tests a putative tumor suppressor gene doc-1 as a regulator of the cell cycle. Three Core Facilities have been created to support the scientific projects. The Administrative Core, in addition to its managerial function, serves the important role of facilitating electronic communication and data sharing among the investigators. The tissue Bank and Pathology Core will collect and bank human oral tumors, and will create a database to compile clinical histories, provide tissues for culturing, and perform HPV typing, in situ hybridization, and immunohistochemistry. The Cell Culture Core will generate cell cultures from normal, premalignant, and malignant human and mouse oral biopsy specimens and will construct sable transductants for the research projects. These Cores will also validate conclusions from the research projects in human oral cancer tissues.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Program Projects (P01)
Project #
5P01DE012467-03
Application #
6176053
Study Section
Special Emphasis Panel (ZDE1-GH (10))
Program Officer
Sandberg, Ann
Project Start
1998-04-01
Project End
2003-03-31
Budget Start
2000-04-01
Budget End
2001-03-31
Support Year
3
Fiscal Year
2000
Total Cost
$940,802
Indirect Cost
Name
Harvard University
Department
Dentistry
Type
Schools of Dentistry
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Crissey, Mary Ann S; Guo, Rong-Jun; Funakoshi, Shinsuke et al. (2011) Cdx2 levels modulate intestinal epithelium maturity and Paneth cell development. Gastroenterology 140:517-528.e8
Guo, Rong-Jun; Funakoshi, Shinsuke; Lee, Hannah H et al. (2010) The intestine-specific transcription factor Cdx2 inhibits beta-catenin/TCF transcriptional activity by disrupting the beta-catenin-TCF protein complex. Carcinogenesis 31:159-66
Funakoshi, Shinsuke; Kong, Jianping; Crissey, Mary Ann et al. (2010) Intestine-specific transcription factor Cdx2 induces E-cadherin function by enhancing the trafficking of E-cadherin to the cell membrane. Am J Physiol Gastrointest Liver Physiol 299:G1054-67
Kalabis, Jiri; Oyama, Kenji; Okawa, Takaomi et al. (2008) A subpopulation of mouse esophageal basal cells has properties of stem cells with the capacity for self-renewal and lineage specification. J Clin Invest 118:3860-9
Oyama, K; Okawa, T; Nakagawa, H et al. (2007) AKT induces senescence in primary esophageal epithelial cells but is permissive for differentiation as revealed in organotypic culture. Oncogene 26:2353-64
Maley, Carlo C; Rustgi, Anil K (2006) Barrett's esophagus and its progression to adenocarcinoma. J Natl Compr Canc Netw 4:367-74
Natarajan, Easwar; Omobono 2nd, John D; Guo, Zongyou et al. (2006) A keratinocyte hypermotility/growth-arrest response involving laminin 5 and p16INK4A activated in wound healing and senescence. Am J Pathol 168:1821-37
Cao, Wenhui; Cavacini, Lisa A; Tillman, Karl C et al. (2005) CD40 function in squamous cell cancer of the head and neck. Oral Oncol 41:462-9
Ishii, Hideshi; Vecchione, Andrea; Furukawa, Yusuke et al. (2004) Differentially expressed genes execute zinc-induced apoptosis in precancerous esophageal epithelium of zinc-deficient rats. Oncogene 23:8040-8
Buajeeb, Waranun; Zhang, Xue; Ohyama, Hiroe et al. (2004) Interaction of the CDK2-associated protein-1, p12(DOC-1/CDK2AP1), with its homolog, p14(DOC-1R). Biochem Biophys Res Commun 315:998-1003

Showing the most recent 10 out of 53 publications