LABORATORY RESEARCH Histone Demethylase JMJD2A Drives Prostate Tumorigenesis through Transcription Factor ETV1 Scientist found that overexpression of lysine-specific demethylase 4A (KDM4A, also known as JMJD2A) was positively correlated with Gleason score and metastasis in human prostate tumors. Overexpression of JMJD2A resulted in the development of prostatic intraepithelial neoplasia in mice, demonstrating that JMJD2A can initiate prostate cancer development. [J Clin Invest] Full Article An Immune-Inflammation Gene Expression Signature in Prostate Tumors of Smokers To identify smoking-induced alterations in human prostate cancer, investigators analyzed gene and protein expression patterns in tumors collected from current, past, and never smokers. [Cancer Res] Abstract Silencing of CD24 Enhances the PRIMA-1-Induced Restoration of Mutant P53 in Prostate Cancer Cells In prostate cancer (PCa) cells, there is CD24-dependent inactivation of mutant p53, but the mechanism and its significance remain largely unknown. Researchers validated this observation and explored the therapeutic potential of targeting CD24 in TP53 mutant PCa cells. [Clin Cancer Res] Abstract Co-Targeting Androgen Receptor Splice Variants and mTOR Signaling Pathway for the Treatment of Castration-Resistant Prostate Cancer Scientists evaluated the efficacy and mechanism of combination therapy to block mTOR activity together with EPI-002, an AR N-terminal domain antagonist that blocks the transcriptional activities of full-length androgen receptor and androgen receptor splice variants in models of castration-resistant prostate cancer. [Clin Cancer Res] Abstract Sildenafil (Viagra) Sensitizes Prostate Cancer Cells to Doxorubicin-Mediated Apoptosis through CD95 Scientists investigated the mechanism by which sildenafil sensitizes doxorubicin (DOX) in killing of prostate cancer (PCa) cells, DU145. The death receptor Fas (APO-1 or CD95) induces apoptosis in many carcinoma cells, which is negatively regulated by anti-apoptotic molecules such as FLIP (Fas-associated death domain (FADD) interleukin-1-converting enzyme (FLICE)-like inhibitory protein). [Oncotarget] Abstract | Full Article Clonal Evaluation of Prostate Cancer Foci in Biopsies With Discontinuous Tumor Involvement by Dual ERG/SPINK1 Immunohistochemistry Scientists hypothesized that spatially distinct prostate cancer foci in biopsies may arise from separate clones, impacting cancer involvement assessment. They used dual ERG/SPINK1 immunohistochemistry to determine the frequency of separate clones—when separate tumor foci showed discordant ERG and/or SPINK1 status—in discontinuously involved prostate biopsy cores from two academic institutions. [Mod Pathol] Abstract Ad5/35E1aPSESE4: a Novel Approach to Marking Circulating Prostate Tumor Cells with a Replication Competent Adenovirus Controlled by PSA/PSMA Transcription Regulatory Elements Investigators established a novel application for detecting PSA/PSMA-positive prostate cancer cells circulating in peripheral blood employing an adenovirus called Ad5/35E1aPSESE4. Ad5/35E1aPSESE4 utilized PSES, a chimeric enhancer derived from PSA/PSMA promoters that is highly active with and without androgen. [Cancer Lett] Abstract | Full Article Mitigation of Arsenic-Induced Acquired Cancer Phenotype in Prostate Cancer Stem Cells by miR-143 Restoration Scientists investigated whether loss of miR-143 expression is important in arsenic-induced transformation of prostate stem/progenitor cells (SCs). Restoration of miR-143 in As-cancer stem cells (CSCs) was achieved by lentivirus-mediated miR-143 overexpression. [Toxicol Appl Pharmacol] Abstract CLINICAL RESEARCH Addition of Docetaxel or Bisphosphonates to Standard of Care in Men with Localised or Metastatic, Hormone-sensitive Prostate Cancer: A Systematic Review and Meta-analyses of Aggregate Data Results from large randomised controlled trials combining docetaxel or bisphosphonates with standard of care in hormone-sensitive prostate cancer have emerged. In order to investigate the effects of these therapies and to respond to emerging evidence, investigators aimed to systematically review all relevant trials using a framework for adaptive meta-analysis. [Lancet Oncol] Abstract | Full Article | Press Release |