Identification and Targeting of Candidate Pre-Existing Lurker Cells that Give Rise to Castration-Resistant Prostate Cancer

Abstract

Castration-resistant prostate cancer (CRPC) is a lethal disease. We lack standard biomarkers to predict hormonal sensitivity of tumors, and we need new targets for therapy to prevent or treat CRPC. The selection theory predicts that pre-existing androgen-independent prostate cancer cells (termed lurker cells) contribute to CRPC, as they are not targeted by androgen deprivation therapy and may be capable of regenerating the tumor. Therefore, targeting these predicted lurker cells in combination with androgen-deprivation therapy would likely prevent or delay the onset of CRPC. The goals of this proposal are to provide functional evidence for intermediate luminal progenitor cells as the pre-existing lurker cells in primary prostate tumors, to evaluate potential therapeutic targets in intermediate luminal progenitor cells, and to define candidate biomarkers in intermediate luminal progenitor cells that can predict prognosis and response to hormonal therapy.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2015
Accession Number
AD1000980

Entities

People

  • Andrew Goldstein

Organizations

  • University of California

Tags

DTIC Thesaurus Topics

  • Androgens
  • Biological Markers
  • Biomedical Research
  • Castration
  • Cells
  • Deprivation
  • Diseases And Disorders
  • Medical Personnel
  • Neoplasms
  • Prostate
  • Prostate Cancer
  • Standards
  • Statistical Analysis
  • Stem Cells
  • Targeting
  • Targets
  • Tissues

Fields of Study

  • Medicine

Readers

  • Molecular Biology and Genetics
  • Prostate Cancer Biology.
  • Systems Analysis and Design