The EphA2 receptor belongs to the recently cloned Eph family of receptor tyrosine kinase (RTK). High levels of EphA2 RTK have been detected in 60-90% of human breast cancer specimens, both in breast cancer cells and in tumor vascular endothelial cells. However, the mechanisms by which EphA2 promotes breast cancer malignancy are not completely clear. In my dissertation work, I first investigated the effect of EphA2 overexpression on tumor cells. I found that increased EphA2 expression in normal epithelial cells contributes to destabilization of cell-cell adhesion, an early step towards tumor cell malignancy; whereas high levels of EphA2 expression in tumor cells increase tumor cell motility and lung metastasis. In addition to regulating tumor cell malignancy, EphA2 also promotes tumor angiogenesis. In order to dissect EphA2 signaling in vascular endothelial cells, I mapped phosphorylated tyrosine residues on the EphA2 receptor, identified interacting proteins that bind to these sites, and tested the effects of a series of phosphorylation-defective EphA2 mutants on angiogenesis. These studies established a critical role for tyrosine phosphorylation of EphA2 in tumor angiogenesis. Taken together, my thesis work demonstrated that EphA2 regulates tumor progression by promoting both tumor cell malignancy and tumor angiogenesis.
| Identifer | oai:union.ndltd.org:VANDERBILT/oai:VANDERBILTETD:etd-08222008-132323 |
| Date | 25 August 2008 |
| Creators | Fang, Wei Bin |
| Contributors | Ann Richmond, Steve Hanks, Jin Chen, Al Reynolds |
| Publisher | VANDERBILT |
| Source Sets | Vanderbilt University Theses |
| Language | English |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | http://etd.library.vanderbilt.edu/available/etd-08222008-132323/ |
| Rights | unrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to Vanderbilt University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. |
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