Targeting LSD1 Epigenetic Signature in Castration-Recurrent Prostate Cancer

Abstract

Prostate cancer (PCa) is the second most common cause of cancer death in men in the US. PCa is initially driven by circulating androgens that activate AR and its downstream targets. AR inhibition is a primary therapeutic intervention but patients often relapse and develop castration recurrent PCa (CRPCa). This is often clinically lethal. Here we describe a potential therapeutic approach for patients that develop CRPCa. We demonstrated that targeting AR and its coregulator LSD1 lead to additive antiproliferative effect in-vitro and potentially reduces CRPCa progression in-vivo. Ongoing studies aim to describe the genome-wide signature of AR and LSD1 in androgen responsive and CRPCa cell lines, in addition to cell lines with DHT-activated AR. Validation of this approach in our pre-clinical studies can have a beneficial impact on PCa patients since it defines a novel therapeutic regiment that relies on already clinically available drugs.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2014
Accession Number
ADA612062

Entities

People

  • Sebastiano Battaglia

Organizations

  • Health Research, Incorporated

Tags

DTIC Thesaurus Topics

  • Additives (Chemicals)
  • Androgen Receptors
  • Androgens
  • Biomedical Research
  • Cancer
  • Castration
  • Cell Line
  • Cells
  • Diseases And Disorders
  • Inhibition
  • Medical Personnel
  • Neoplasms
  • Prostate
  • Prostate Cancer
  • Targeting
  • Targets
  • Therapy

Fields of Study

  • Biology
  • Medicine

Readers

  • Prostate Cancer Biology.