Accession Number:

ADA446982

Title:

Anticar Inhibitors of AR-Mediated Gene Expression

Descriptive Note:

Annual rept. 1 Nov 2004-31 Oct 2005

Corporate Author:

PENNSYLVANIA STATE UNIV UNIVERSITY PARK

Personal Author(s):

Report Date:

2005-11-01

Pagination or Media Count:

19.0

Abstract:

New drugs that halt the progression of prostate cancers are urgently needed. Because many prostate cancers require the androgen dihydrotestosterone to proliferate, antiandrogens such as casodex bicalutamide are often the first line therapy for treatment of this disease. However, this drug and other clinically employed antiandrogens generally suffer from low affinity for the androgen receptor AR, low selectivity across the nuclear hormone receptor superfamily, and do not achieve complete androgen blockade. As an alternative, mifepristone RU486 is under investigation as a potential anticancer agent effective against prostate cancers. This drug is a highly potent antiprogestin 1050 25 pM but also exhibits potent antiglucocorticoid 1050 2.2 nM and antiandrogen 1050 10 nM activities. Although mifepristone is effective against prostate cancer cells in vivo, the use of this drug as a chronically administered anticancer agent is severely limited by its potent antiglucocorticoid activity. We are investigating novel anticancer agents structurally related to mifepristone but that are designed to lack the antiglucocorticoid activity associated with this drug.

Subject Categories:

  • Biochemistry
  • Anatomy and Physiology
  • Medicine and Medical Research

Distribution Statement:

APPROVED FOR PUBLIC RELEASE