Castration-Resistant Prostate Cancer Castration-resistant prostate cancer (CRPC) directly contributes to patient mortality. It is imperative to develop new and effective adjunct therapy to enhance the response of CRPC to hormonal therapy. Recently we developed ProFineTM, a proprietary formula consisting of bioactive flavonoids enriched in pomegranate fruit, and demonstrated its potent anti-cancer activity in CRPC cells. In this Phase I STTR application, we hypothesize that ProFineTM potently co-targets AR and Akt signaling, thereby activating apoptosis in CRPC cells and sensitizing them to androgen deprivation therapy (ADT).
Two Aims are proposed:
Aim 1 will determine the mechanism of action of ProFineTM in CRPC cells, specifically how ProFineTM inhibits androgen receptor signaling;
Aim 2 will evaluate the efficacy of ProFineTM in enhancing enzalutamide hormonal therapy in an orthotopic model of CRPC. Accomplishment of the proposed studies will provide solid evidence for future patent application and a Phase II STTR application.

Public Health Relevance

American Cancer Society estimated that 233,000 new cases will be diagnosed with prostate cancer (PCa) in 2014 and 29,480 patients will die, mostly from castration-resistant disease (CRPC). It is imperative to develop safe, efficacious and cost-effective adjunct therapy to enhance the response of CPRC to standard therapies. In this Phase I STTR application, we will develop ProFineTM, a pomegranate-derived flavonoid formula, as an effective adjunct treatment to enzalutamide therapy in CRPC. It is expected that as a dietary supplement, ProFineTM can be rapidly commercialized and approved for clinical trials. This proposal has profound impact due to its immediate potentia l in treating a lethal disease, reducing cancer morbidity and improving healthcare in the United States and globally.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Small Business Technology Transfer (STTR) Grants - Phase I (R41)
Project #
1R41CA186498-01A1
Application #
8834755
Study Section
Special Emphasis Panel (ZRG1-OTC-T (10))
Program Officer
Weber, Patricia A
Project Start
2015-03-01
Project End
2016-02-29
Budget Start
2015-03-01
Budget End
2016-02-29
Support Year
1
Fiscal Year
2015
Total Cost
$160,996
Indirect Cost
Name
Metcure Therapeutics, LLC
Department
Type
DUNS #
078866511
City
Atlanta
State
GA
Country
United States
Zip Code
30341
Hooshfar, Shirin; Linzey, Michael R; Wu, Daqing et al. (2018) Sensitive liquid chromatography/tandem mass spectrometry method for the determination of two novel highly lipophilic anticancer drug candidates in rat plasma and tissues. Biomed Chromatogr 32:
Mamouni, Kenza; Zhang, Shumin; Li, Xin et al. (2018) A Novel Flavonoid Composition Targets Androgen Receptor Signaling and Inhibits Prostate Cancer Growth in Preclinical Models. Neoplasia 20:789-799
Yang, Yang; Mamouni, Kenza; Li, Xin et al. (2018) Repositioning Dopamine D2 Receptor Agonist Bromocriptine to Enhance Docetaxel Chemotherapy and Treat Bone Metastatic Prostate Cancer. Mol Cancer Ther 17:1859-1870
Wu, Daqing (2017) Epithelial protein lost in neoplasm (EPLIN): Beyond a tumor suppressor. Genes Dis 4:100-107
Yang, Yang; Li, Xin; Mamouni, Kenza et al. (2017) Mifepristone Has Limited Activity to Enhance the In Vivo Efficacy of Docetaxel and Enzalutamide Against Bone Metastatic and Castration-Resistant Prostate Cancer. Anticancer Res 37:6235-6243
Liu, Hong Yan; Yu, Xiaolin; Liu, Haitao et al. (2016) Co-targeting EGFR and survivin with a bivalent aptamer-dual siRNA chimera effectively suppresses prostate cancer. Sci Rep 6:30346
Zhang, Shumin; Gera, Lajos; Mamouni, Kenza et al. (2016) Inhibition of skeletal growth of human prostate cancer by the combination of docetaxel and BKM1644: an aminobisphosphonate derivative. Oncotarget 7:27489-98
Pu, Fan; Salarian, Mani; Xue, Shenghui et al. (2016) Prostate-specific membrane antigen targeted protein contrast agents for molecular imaging of prostate cancer by MRI. Nanoscale 8:12668-82