Salivary gland function is important in maintaining normal oral health, as well as playing a critical role in proper digestion. Normal salivary gland function and homeostasis is dependent upon the balance of cell growth, maintenance of cellular differentiation and cell death. Several million people in the United States suffer from benign and malignant tumors of the major and minor salivary glands and salivary gland hypofunction. Salivary gland hypofunction can be caused by chronic drug treatment, particularly in the elderly, Sjorgen's syndrome, an autoimmune disease, X-ray irradiation and cancer chemotherapy. In each of these disease conditions, salivary gland function may be compromised by the loss of the acinar cells or loss of glandular homeostasis due to aberrant apoptosis. The long range goal of this Program Project is to provide the fundamental information that is necessary to fully understand salivary acinar apoptosis at the molecular level. The development of such basic scientific information is essential in understanding the molecular basis of salivary gland tumor development and for the development of new therapeutic modalities for the treatment of prevention of salivary gland hypofunction caused by aberrant apoptosis. Project One will evaluate the role of the caspase and Bcl-2 superfamilies in salivary acinar apoptosis. Project Two will evaluate the role of the MAPK and Akt signal transduction pathways in regulating acinar apoptosis. Project Three will investigate the role of the protein kinase C family of regulatory proteins in suppressing and/or enhancing genotoxic agents and the onset of apoptosis. A fundamental understanding of how important intracellular signal transduction pathways along with the initiators and effectors of salivary acinar apoptosis is the first step in the development of new therapeutic strategies for the treatment of salivary gland hypofunction in neoplastic development.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Program Projects (P01)
Project #
1P01DE012798-01A1
Application #
6027898
Study Section
Special Emphasis Panel (ZDE1-GH (46))
Program Officer
Zhang, Guo He
Project Start
2000-02-15
Project End
2005-01-31
Budget Start
2000-02-15
Budget End
2001-01-31
Support Year
1
Fiscal Year
2000
Total Cost
$950,087
Indirect Cost
Name
University of Colorado Denver
Department
Other Basic Sciences
Type
Schools of Dentistry
DUNS #
065391526
City
Aurora
State
CO
Country
United States
Zip Code
80045
Limesand, Kirsten H; Said, Sherif; Anderson, Steven M (2009) Suppression of radiation-induced salivary gland dysfunction by IGF-1. PLoS One 4:e4663
Limesand, Kirsten H; Schwertfeger, Kathryn L; Anderson, Steven M (2006) MDM2 is required for suppression of apoptosis by activated Akt1 in salivary acinar cells. Mol Cell Biol 26:8840-56
DeVries, Tracie A; Kalkofen, Rachelle L; Matassa, Angela A et al. (2004) Protein kinase Cdelta regulates apoptosis via activation of STAT1. J Biol Chem 279:45603-12
Limesand, Kirsten H; Barzen, Katherine A; Sanders, Linda A et al. (2003) Characterization of rat parotid and submandibular acinar cell apoptosis in primary culture. In Vitro Cell Dev Biol Anim 39:170-7
Limesand, K H; Barzen, K A; Quissell, D O et al. (2003) Synergistic suppression of apoptosis in salivary acinar cells by IGF1 and EGF. Cell Death Differ 10:345-55
DeVries, Tracie A; Neville, Margaret C; Reyland, Mary E (2002) Nuclear import of PKCdelta is required for apoptosis: identification of a novel nuclear import sequence. EMBO J 21:6050-60
Matassa, A A; Carpenter, L; Biden, T J et al. (2001) PKCdelta is required for mitochondrial-dependent apoptosis in salivary epithelial cells. J Biol Chem 276:29719-28