Role of Reactive Stroma in Prostate Cancer Progression

Abstract

The purpose of this project is to determine the role of fibroblast growth factor (FGF) receptor 1 in reactive stroma during prostate tumorigenesis. The authors are using a novel approach to target transgene expression specifically to the reactive stroma of experimental prostate cancer. They are placing an inducible Cre recombinase (CrePR1) into the fibroblast activation protein (FAP) gene locus to target expression to reactive stroma. They will cross this mouse with Fgfr1flox mice (LoxP sites flanking FGF receptor 1 alleles, which are cognate receptors for FGF-2). These mice will be crossed with TRAMP mice (prostate cancer model). Induced expression of Cre at sites of reactive stroma generated in the cancer foci will function to excise the FGF receptor 1 alleles and create a conditional knockout mouse. Progression of tumorigenesis in this line of knockout mice will be compared to heterozygous and wild type controls. Progress has been made in each Task. The authors have completed all cloning steps and acquired all reagents. They have rederived the Fgfr1flox and have crossed it into the appropriate backgrounds. In addition, they have completed crossing the TRAMP mice with the Fgfr1flox mice. This study will pinpoint the role of FGF receptor 1 in reactive stroma promotion of prostate cancer progression.

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Document Details

Document Type
Technical Report
Publication Date
Feb 01, 2006
Accession Number
ADA448231

Entities

People

  • David R. Rowley

Organizations

  • Baylor College of Medicine

Tags

DTIC Thesaurus Topics

  • Anti-Bacterial Agents
  • Biological Factors
  • Carcinoma
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Culture Media
  • Fibroblasts
  • Gene Expression
  • Genetics
  • Neoplasms
  • Peptide Growth Factors
  • Peptides
  • Prostate Cancer
  • Proteins

Readers

  • Molecular Biology and Genetics
  • Oncology (Cancer Research).