Angiostatic Therapy: A New Treatment Modality for Prostate Cancer

Abstract

The overall goal is to investigate if blockade of vascular endothelial growth factor in combination with conventional cytotoxic agents could be a new innovative treatment regimen for hormone-refractory prostate cancer. We proposed to use our in vivo model to examine the capacity of a soluble VEGF receptor fusion protein (flt-lgG) to inhibit angiogenesis and growth of tumor tissue derived from patients and compare with established prostate cancer cell lines. We experienced very poor growth of prostate carcinoma implanted in our in vivo system, however, since the stroma plays a pivotal role in prostate cancer progression, we hypothesized that the model would be much improved if we were to develop a more 'orthotopic milieu'. To achieve this goal, we implanted murine prostate tissue prior to implantation of tumor spheroids. Interestingly, adult prostate tissue becomes highly re-vascularized. However, the murine stroma did not much affect growth of human biopsies, but, growth of the murine prostate carcinoma cell line TRAMP C2, was significantly enhanced. We hypothesized, that the 'stromal factors' are species specific. We therefore isolated peritumor fibroblasts from one of our biopsies and mixed these with the tumor cells, which resulted in significantly higher growth rates. We had proposed to label tumor cells with an in vivo dye (CMTMR), but due to serious limitations with the in vivo dye, we introduced a histone-GFP fusion protein as a marker for our tumor cells. This labeling technique allows us to evaluate not only tumor size, but also mitotic and apoptotic indices of the implanted tumor spheroids. With these significant and necessary modifications we have a unique pseudo-orthotopic model, which allows us to evaluate, in prostate cancer, in detail the underlying mechanisms behind chemotherapy and angiostatic mediated tumor regression.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Jan 01, 2000
Accession Number
ADB261475

Entities

People

  • Per Borgström

Tags

DTIC Thesaurus Topics

  • Blood
  • Breast Cancer
  • Cancer
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Cytotoxins
  • Growth Factors
  • Medical Personnel
  • Microvessels
  • Neoplasms
  • Peptides
  • Prostate
  • Prostate Cancer
  • Proteins
  • Side Effects

Fields of Study

  • Medicine

Readers

  • Oncology (Cancer Research).