Isolation of Genes Involved in Human Prostate Cancer Progression by Functional Expression Cloning

Abstract

During phase I of this IDEA Award, we examined mechanisms of androgen independent prostate cancer progression using our LAPC xenograft model. Our focus was to identify genes and/or signaling pathways that might be responsible for androgen independent growth, through expression cloning. We have successfully identified several such candidates through screening xenografts and validated the activity of these candidates in xenograft models. Our current focus is to study two genes/pathways that were identified in this screen (the EGFR/Her2 pathway and the cathepsin D protease) as tools to create new transgenic models of prostate cancer. We are also developing a new transgenic model using the avian retrovirus receptor TVA that will allow us to introduce multiple transgenes into the prostate in a stepwise manner and to manipulate androgen levels without affecting transgene expression (as part of the Phase II grant).

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Document Details

Document Type
Technical Report
Publication Date
Feb 01, 2001
Accession Number
ADA391693

Entities

People

  • Charles Sawyers

Organizations

  • University of California, Los Angeles

Tags

DTIC Thesaurus Topics

  • Androgen Receptors
  • Androgens
  • Biomedical Research
  • Breast Cancer
  • Cancer
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Chemical Compounds
  • Chemistry
  • Genetic Structures
  • Hormones
  • Neoplasms
  • Prostate
  • Prostate Cancer
  • Proteins
  • Xenografts

Fields of Study

  • Biology

Readers

  • Molecular Biology and Genetics
  • Molecular and genetic basis of cancer.
  • Oncology (Cancer Research).