Targeting Androgen Receptor Function by MicroRNA in Prostate Cancer

Abstract

Prostate cancer is the most commonly diagnosed and second most deadly cancer in North American men and the blockade of androgen action through the AR has been the cornerstone of systemic therapy of prostate cancer. The failure of AR receptor antagonists results in higher levels of AR protein which promotes the development of androgen-independent prostate cancer. Originally we proposed the utilization of micro (mi) RNAs to blockade the expression of AR in prostate carcinoma cells. We have identified a miRNAs that can repress the AR protein synthesis in prostate carcinoma cells. Our long-term goals are to identify naturally occurring miRNAs that have potential to block the activity of AR and to improvise their efficacy by rational designing to provide novel 'AR Antagonist miRNAs'.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 2009
Accession Number
ADA520784

Entities

People

  • Girish C. Shukla

Organizations

  • Cleveland State University

Tags

DTIC Thesaurus Topics

  • Acquisition
  • Androgen Receptors
  • Androgens
  • Biomedical Research
  • Biomolecules
  • Cells
  • Chemical Compounds
  • Culture Techniques
  • Department Of Defense
  • Information Operations
  • Neoplasms
  • Prostate
  • Prostate Cancer
  • Proteins
  • Ribonucleic Acids
  • Targets
  • Transfection

Readers

  • Oncology and Biomarker-Based Cancer Detection.
  • Prostate Cancer Biology.