SBIR/STTR Research Award
CELL-BASED HIGH THROUGHPUT SCREENING FOR ANTI-ANDROGENS
Award amount
$100,000Program and phase
SBIR · Phase IAward year
2002Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- ANDROSCIENCE CORPORATION
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
DESCRIPTION (provided by the applicant): Prostate cancer is the most frequently
diagnosed cancer in American men and the second leading cause of male cancer
death. Antiandrogens have been used with castration to prevent the progression
of prostate cancer. However, cancer relapse often occurs within 2-3 years in
patients who received this therapy. This has prompted interest in developing
better antiandrogens for prostate cancer treatment. Traditional Chinese Herbal
Medicines (TCHM) have been shown to block recurrent prostate cancer growth. In
our preliminary study, using a newly-developed androgen receptor (AR) and
androgen receptor co-activator (ARA)-mediated transactivation assay, it was
found that some extracts from TCHM inhibited AR-induced gene activation,
suggesting TCHM is an excellent source to search for new antiandrogen drugs. A
cell-based androgen/AR activation assay developed from this study is
advantageous in discovering antiandrogens that exert their inhibitory function
at different stages of an androgen-induced gene activation. Performing this
assay could lead to the discovery of potentially new and different antiandrogen
drugs. Conventional antiandrogens only interfere with androgen and AR binding,
such as HF (hydroxyflutamide) or casodex (bicalutamide). In this application we
propose to develop a high throughput 96-well format AR/ARA transactivation
assay using three prostate cancer cell lines: DU145, PC3 and LNCaP. In
collaboration with our corporate partner, Plantaceutica Inc. (Chapel Hill, NC),
a large number of extracts and compounds from TCHM that are known to possess
ingredients with potential antiandrogen and androgenic activities will be
screened. Compounds from TCHM extracts with effects to block wild type AR and
mutant AR transactivation in all three human prostate cancer cell models will
be further tested in a proliferation assay using androgen-sensitive prostate
cancer, LNCaP cells to assess their biological efficacy in suppressing prostate
cancer cell growth. Compounds discovered by our study with antiandrogenic or
androgenic activities will have great potential to be developed into new drugs
that will improve the treatment of prostate cancer patients and other androgen
related disorders.
PROPOSED COMMERCIAL APPLICATION:
NOT AVAILABLE
Technology keywords
Not reported