Inhibitors of Fatty Acid Synthase for Prostate Cancer

Abstract

The purpose of this proposal was to develop and optimize chemical scaffolds as potential inhibitors of fatty acid synthase (FASN), specifically the thioesterase (TE) domain. This line of investigation was based on a series of observation by many groups, including ours, that FASN represents a valuable drug target. It isoverexpressed in prostate cancer and appears to be required for tumor cells to survive. Through an iterative scheme of in silico design, activity-based screening and structural analyses we identified a series of novel pharmacophores with the ability to inhibit the thioesterase domain of FASN. This proposal had three specific aims. They were 1) To optimize compounds through structure-based design, chemical syntheses and in vitro testing, 2) To determine the toxicological and pharmacokinetic properties of the most promising analog(s), and 3) To test the efficacy of the analog(s) in mouse xenograft models of human prostate cancer. Here we summarize the findings by our group during the course of the research proposal.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
May 01, 2012
Accession Number
ADA570535

Entities

People

  • Steven J. Kridel

Organizations

  • Wake Forest University

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • 2-Ring Heterocyclic Compounds
  • Biochemistry
  • Biomedical Research
  • Carrier Proteins
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Department Of Defense
  • Fatty Acids
  • Inhibition
  • Inhibitors
  • Intellectual Property
  • Neoplasms
  • Prostate
  • Prostate Cancer
  • Proteins
  • Quinones

Readers

  • Molecular and Cellular Biochemistry
  • Prostate Cancer Biology.