Blood vessels consist of two interacting cell types: endothelial cells, which form the inner lining of the vascular tube, and pericytes, which wrap around the vascular tube. While endothelial cells are the better characterized of the two, pericytes are now coming into focus as potentially important regulators of tumor angiogenesis. Pericytes constitute a heterogeneous population of cells, and their ontogeny and function, specifically in tumors, is not well understood. This project will test the hypothesis that tumor-associated PDGFRbeta+ perivascular cells are progenitor cells that have the capacity to differentiate into mature pericytes and that they are a critical vascular cell constituent for the maintenance and growth of tumor vessels.
Specific Aim 1. Identify and characterize PDGFRbeta+ perivascular cells in normal and malignant tissues. We will characterize PDGFRbeta+ perivascular cells in three tumor types and in the respective normal tissues.
Specific Aim 2. Study function of PDGFRbeta+ perivascular cells in tumor angiogenesis. We will examine the potential role of PDGFRbeta+ cells as pericyte progenitor cells and as survival mediators for endothelial cells.
Specific Aim 3. Reveal the origin of PDGFRbeta+ perivascular cells in tumor angiogenesis. We will test whether tumor-associated PDGFRbeta+ perivascular cells originate from the bone marrow, or from adjacent normal tissue in which the tumor is embedded. The research addresses a novel aspect in tumor angiogenesis. It will test the hypothesis that the tumor-associated pericyte, the PDGFRbeta+ perivascular cell (PVC), is a functional and instrumental component of tumor vessels. The results will set an important foundation for therapeutic implications by exploiting PDGFRbeta+ PVC not only as novel targets for anti-angiogenic therapies in tumors but also as potentially important vascular cell constituents in tissues in which new and stable blood vessel formation is desired.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA109390-01
Application #
6816972
Study Section
Special Emphasis Panel (ZRG1-TME (01))
Program Officer
Mohla, Suresh
Project Start
2004-08-01
Project End
2009-07-31
Budget Start
2004-08-01
Budget End
2005-07-31
Support Year
1
Fiscal Year
2004
Total Cost
$240,859
Indirect Cost
Name
University of California San Francisco
Department
Neurosurgery
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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Du, Rose; Lu, Kan V; Petritsch, Claudia et al. (2008) HIF1alpha induces the recruitment of bone marrow-derived vascular modulatory cells to regulate tumor angiogenesis and invasion. Cancer Cell 13:206-20
Lamagna, Chrystelle; Bergers, Gabriele (2006) The bone marrow constitutes a reservoir of pericyte progenitors. J Leukoc Biol 80:677-81
Bergers, Gabriele; Song, Steven (2005) The role of pericytes in blood-vessel formation and maintenance. Neuro Oncol 7:452-64
Song, Steven; Ewald, Andrew J; Stallcup, William et al. (2005) PDGFRbeta+ perivascular progenitor cells in tumours regulate pericyte differentiation and vascular survival. Nat Cell Biol 7:870-9