This section deals with approaches to delineate mechanisms that control collagen synthesis/deposition with angiogenic activities in wounds.
Our aim i s to explore how metabolic conditions in wounds activate collagen gene transcription and collagen synthesis presumably via ADPRibosylation. Oxidant insults and heat shock injury also involve ADPRibosylation. As an alternative means to implicate ADPR mechanisms, as well as a means to open an area of investigation of wound pathology, we propose to determine whether oxygen radicals, DNA damage/repair, and heat shock proteins modulate collagen synthesis. These studies will be conducted in early passage culture of human skin fibroblasts. These studies are expected to provide a firm basis of understanding the how and why collagen synthesis and angiogenesis start, slow down, and stop in healing tissue.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center (P50)
Project #
5P50GM027345-22
Application #
6564559
Study Section
Project Start
2002-01-01
Project End
2002-12-31
Budget Start
Budget End
Support Year
22
Fiscal Year
2002
Total Cost
$203,634
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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Boudreau, Nancy; Myers, Connie (2003) Breast cancer-induced angiogenesis: multiple mechanisms and the role of the microenvironment. Breast Cancer Res 5:140-6

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