Tumors are dependent upon new blood vessel formation, or angiogenesis, for expansive growth. Our recent analysis of gene expression led to the identification of several genes upregulated in endothelial cells that line tumor blood vessels, called Tumor endothelial markers (TEMs). Two of these, TEM5 and TEM8 are of particular interest because they reside on the cell surface and may therefore be directly accessible to blood-borne therapeutics. In an attempt to understand the functional role of TEM5 and TEM8 in angiogenesis, we have begun to generate TEM5 and TEM8 gene knockouts. Because these genes are also likely to be involved developmental angiogenesis we are generating conditional floxed alleles using cre/flp technology such that the gene can be disrupted specifically in adult tissues. By challenging gene disrupted mice with tumors, we hope to determine if either of these genes is critical for tumor angiogenesis. The studies should also allow us to better understand the function of these genes in angiogenesis.

Agency
National Institute of Health (NIH)
Institute
Division of Basic Sciences - NCI (NCI)
Type
Intramural Research (Z01)
Project #
1Z01BC010484-02
Application #
7058628
Study Section
(MCGP)
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2004
Total Cost
Indirect Cost
Name
Basic Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Cullen, Mike; Seaman, Steven; Chaudhary, Amit et al. (2009) Host-derived tumor endothelial marker 8 promotes the growth of melanoma. Cancer Res 69:6021-6
Nanda, Akash; Carson-Walter, Eleanor B; Seaman, Steven et al. (2004) TEM8 interacts with the cleaved C5 domain of collagen alpha 3(VI). Cancer Res 64:817-20