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Yazici S., Kim S., Busby J., He J., Thaker P., Yokoi K., ...More
PROSTATE, vol.65, no.3, pp.203-215, 2005 (SCI-Expanded)
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Publication Type:
Article / Article
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Volume:
65
Issue:
3
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Publication Date:
2005
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Doi Number:
10.1002/pros.20283
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Journal Name:
PROSTATE
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Journal Indexes:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Page Numbers:
pp.203-215
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Keywords:
prostate cancer, EGF-R and VEGF-R phosphorylation, antivascular therapy, RECEPTOR TYROSINE KINASE, CELL LUNG-CANCER, MICROVASCULAR HYPERPERMEABILITY, CLINICAL-SIGNIFICANCE, EGF RECEPTOR, TUMOR-CELLS, EXPRESSION, ANGIOGENESIS, PROGRESSION, BLOCKADE
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Hacettepe University Affiliated:
Yes
Abstract
BACKGROUND. Androgen-independent prostate cancer (PCa) may be susceptible to modulation of the tumor microenvironment. We determined whether a dual tyrosine kinase inhibitor (AEE788) of the epidermal growth factor receptor (EGF-R) and vascular endothelial growth factor receptor (VEGF-R) combined with chemotherapy can produce therapy of human PCa in nude mice.