LABORATORY RESEARCH Notch Pathway Inhibition Using PF-03084014, a γ-Secretase Inhibitor (GSI), Enhances the Anti-Tumor Effect of Docetaxel in Prostate Cancer The effect of PF-03084014 on response to docetaxel was evaluated in docetaxel-sensitive and -resistant castration-resistant prostate cancer cell lines in vitro and in murine models. Impacts on cell proliferation, apoptosis, cancer stem cells and angiogenesis were evaluated. [Clin Cancer Res] Abstract The Use of Collagen-Based Scaffolds to Simulate Prostate Cancer Bone Metastases with Potential for Evaluating Delivery of Nanoparticulate Gene Therapeutics Scientists established a 3D cell culture model of prostate cancer bone metastasis using collagen-based scaffolds, characterized this model, and assessed the potential of the model to evaluate delivery of gene therapeutics designed to target bone metastases. [Biomaterials] Abstract Hypoxia-Inducible miR-182 Enhances HIF1α Signaling via Targeting PHD2 and FIH1 in Prostate Cancer Overexpression of miR-182 in prostate cancer cells led to a reduction of prolyl hydroxylase domain enzyme 2 (PHD2) and factor inhibiting hypoxia-inducible factor 1 (HIF-1) (FIH1) expression and an increase in HIF1α level either under normoxic or hypoxic condition. [Sci Rep] Full Article TRAIL-Troglitazone-Induced Apoptosis in Prostate Cancer Cells Involve AMP-Activated Protein Kinase Since troglitazone is known to activate AMP-activated protein kinase (AMPK), the authors determined whether AMPK is a molecular target mediating this apoptotic cascade by utilizing prostate cancer cell lines stably overexpressing AMPKα1-dominant negative or empty vector. [J Biol Chem] Abstract | Full Article Delivery of Retinoic Acid to LNCap Human Prostate Cancer Cells Using Solid Lipid Nanoparticles Anticancer efficiency was evaluated by incubating retinoic acid-solid lipid nanoparticles (SLNs) with human prostate cancer (LNCap) cells, which demonstrated reduced cell viability with increased drug concentrations while blank SLNs displayed negligible cytotoxicity. [Int J Pharm] Abstract Pituitary Tumor-Transforming Gene 1 Regulates Invasion of Prostate Cancer Cells through MMP13 In vitro, pituitary tumor-transforming gene 1 (Pttg1) activated matrix metalloproteinase 13 (MMP13), which determined prostate cancer (PC) cell invasiveness. However, Pttg1 levels were not significantly affected by MMP13. Furthermore, the Pttg1-activated MMP13 in PC cells was significantly suppressed by inhibition of PI3k/Akt, but not ERK/MAPK or JNK pathways. [Tumour Biol] Abstract Targeted Nanomedicine for Prostate Cancer Therapy: Docetaxel and Curcumin Co-Encapsulated Lipid–Polymer Hybrid Nanoparticles for the Enhanced Anti-Tumor Activity In Vitro and In Vivo Docetaxel and curcumin co-encapsulated lipid–polymer hybrid nanoparticles (LPNs) were constructed. The cytotoxicity of the LPNs was evaluated on PC-3 human prostate carcinoma cells by MTT assays. [Drug Deliv] Abstract The GnRH Antagonist Degarelix Directly Inhibits Benign Prostate Hyperplasia Cell Growth Benign prostate hyperplasia (BPH)-isolated epithelial and stromal cells were either cultured alone or co-cultured and subsequently treated with increasing concentrations of degarelix. Degarelix treatment induced a decrease in cell viability and cell proliferation rates, which occurred in parallel to an increase in apoptosis. [Horm Metab Res] Abstract CLINICAL RESEARCH Novel Biomarker Signature that May Predict Aggressive Disease in African American Men with Prostate Cancer Scientists studied the ethnicity-specific expression of prostate cancer (PC)–associated biomarkers to evaluate whether genetic/biologic factors affect ethnic disparities in PC pathogenesis and disease progression. [J Clin Oncol] Abstract | Press Release Efficacy of Cabazitaxel in Castration-Resistant Prostate Cancer Is Independent of the Presence of AR-V7 in Circulating Tumor Cells The authors investigated the association between androgen receptor splice variant 7 (AR-V7) expression in circulating tumor cells and resistance to cabazitaxel. They selected patients with metastatic castration-resistant prostate cancer (mCRPC) from the multicenter, randomized, Phase II, open-label study in mCRPC on the pharmacodynamic effects of budesonide on cabazitaxel. [Eur Urol] Abstract |