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The Role of EphA2 RTK in Breast Cancer Cell Malignancy and Tumor Angiogenesis

dc.creatorFang, Wei Bin
dc.date.accessioned2020-08-22T20:50:52Z
dc.date.available2010-08-25
dc.date.issued2008-08-25
dc.identifier.urihttps://etd.library.vanderbilt.edu/etd-08222008-132323
dc.identifier.urihttp://hdl.handle.net/1803/13970
dc.description.abstractThe 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.
dc.format.mimetypeapplication/pdf
dc.subjectReceptor Tyrosine Kinase
dc.subjectBreast Cancer
dc.subjectEphA2
dc.subjectNeovascularization -- Regulation
dc.subjectProtein-tyrosine kinase -- Receptors
dc.titleThe Role of EphA2 RTK in Breast Cancer Cell Malignancy and Tumor Angiogenesis
dc.typedissertation
dc.contributor.committeeMemberAnn Richmond
dc.contributor.committeeMemberSteve Hanks
dc.contributor.committeeMemberJin Chen
dc.type.materialtext
thesis.degree.namePHD
thesis.degree.leveldissertation
thesis.degree.disciplineCancer Biology
thesis.degree.grantorVanderbilt University
local.embargo.terms2010-08-25
local.embargo.lift2010-08-25
dc.contributor.committeeChairAl Reynolds


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