Killing Prostate Cancer Cells and Endothelial Cells with a VEGF-Triggered Cell Death Receptor

Abstract

The goal of this project was to test a novel chimeric cell death receptor (termed R2Fas) that is triggered by vascular endothelial growth factor (VEGF), as a means to kill prostate cancer cells and vascular endothelial cells. The scope of this project involved: (i) creating adenoviral reagents to express the R2Fas receptor in prostate cancer cells and endothelial cells; (ii) determining if the R2Fas receptor kills cells in a VEGF-dependent manner; and (iii) identifying methods for increasing the killing activity of R2Fas. The major findings were: (i) we generated replication-defective adenoviral reagents to express R2Fas as well as control adenoviruses; (ii) we demonstrated that adenoviral-mediated expression of R2Fas in prostate cancer cells that overexpress VEGF activates apoptotic signaling and induces cell death; (iii) we demonstrated that adenoviral-mediated expression of R2Fas in human endothelial cell is non-toxic, but rendered the cells sensitive to killing when treated with VEGF; and (iv) we demonstrated that R2Fas-mediated apoptosis can be potentiated by addition of several pharmacologic agents, including camptothecin, etoposide, taxol, doxorubicin, cisplatin, and BisVIII.

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 2005
Accession Number
ADA476159

Entities

People

  • Timothy P. Quinn

Organizations

  • University of California, San Francisco

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Adenoviruses
  • Alkaloids
  • Apoptosis
  • Blood Vessels
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Department Of Defense
  • Endothelial Cells
  • Epithelial Cells
  • Growth Factors
  • Medical Personnel
  • Neoplasms
  • Prostate
  • Prostate Cancer
  • Therapy
  • Viruses

Fields of Study

  • Biology

Readers

  • Breast cancer cell signaling and growth regulation.
  • Cellular and Molecular Pathways of Apoptosis.
  • Immunology and Pathology