Treatment of Prostate Cancer by Targeting Vascular Endothelial Growth Factor Receptors (VEGFRs) and Micrometastases with Bismuth-213 Labeled Vectors

Abstract

The main purpose of the proposed study was to evaluate the toxicity and efficacy of multiple targeting vectors for the treatment of prostate cancer in mouse models. After successfully achieving the in vitro outcomes, the in vivo studies have also proven to be a great success. The efficacy of the proposed combination therapy has proven to be far better than the mono-therapy and the results are significantly different. Various combination therapy regimes were well tolerated in mice whereas the long-term toxicity studies are currently ongoing. The dose optimization, time interval optimization and subcutaneous efficacy studies have been completed whereas orthotopic model studies are expected to be complete in three months. Thus the in vitro (radiolabeling of Avastin, in vitro stability, enhancement of plasminogen activation expression and estimation of VEGF secretion by various prostate cancer cell lines) and in vivo studies have gone as per expectations and plan.

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Document Details

Document Type
Technical Report
Publication Date
Nov 01, 2007
Accession Number
ADA482637

Entities

People

  • Syed M. Abbas Rizvi

Organizations

  • University of New South Wales

Tags

DTIC Thesaurus Topics

  • Cell Line
  • Cells
  • Combination Therapy
  • Growth Factors
  • Intervals
  • Medical Personnel
  • Neoplasms
  • Optimization
  • Plasminogen
  • Prostate
  • Prostate Cancer
  • Proteins
  • Targeting
  • Therapy
  • Time Intervals
  • Toxicity

Fields of Study

  • Medicine

Readers

  • Adaptive Control and Estimation with Uncertainty in Dynamic Systems.
  • Oncology (Cancer Research).