Latarani, Maryam and Pucci, Perla and Eccleston, Mark and Manzo, Massimiliano and Gangadharannambiar, Priyadarsini and Fischetti, Irene and Alborelli, Ilaria and Mongiardini, Vera and Mahmood, Namra and Colombo, Mario Paolo and Grimaldi, Benedetto and Rigas, Sushila and Akamatsu, Shusuke and Hawkes, Cheryl and Wang, Yuzhuo and Jachetti, Elena and Crea, Francesco (2025) EZH2 inhibition enhances the activity of Carboplatin in aggressive-variant prostate cancer cell lines. Epigenomics, 17 (3). pp. 145-154. ISSN 1750-1911
Full text not available from this repository.Abstract
Background Aggressive Variant Prostate Cancers (AVPCs) are incurable malignancies. Platinum-based chemotherapies are used for the palliative treatment of AVPC. The Polycomb Repressive Complex 2 (PRC2) promotes prostate cancer progression via histone H3 Lysine 27 tri-methylation (H3K27me3). EZH2 encodes the catalytic subunit of PRC2. A recently developed nucleosome capture technology (Nu.QⓇ).measures H3K27me3 levels in biological fluids. EZH2 inhibitors (EZH2i) are being tested in clinical trials. We hypothesize that epigenetic reprogramming via EZH2i improves the efficacy of Carboplatin in AVPC and that EZH2i activity can be measured via both cellular- and cell-free nucleosomal H3K27me3 (cf-H3K27me3) levels. Methods We studied the expression of PRC2 genes in clinical prostate cancer cohorts (bioinformatics). We determined the effect of EZH2i on cellular- and cf-H3K27me3 levels. We measured dose-dependent effects of Carboplatin with/without EZH2i on AVPC cell viability (IC50). We used RNA-Seq to study how EZH2i modulates gene expression in AVPC cells. Results PRC2 genes were significantly up-regulated in AVPC vs other prostate cancer types. EZH2i reduced both cellular and cf-H3K27me3 levels. EZH2i significantly reduced Carboplatin IC50. EZH2i reduced the expression of DNA repair genes and increased the expression of p53-dependent pro-apoptotic factors. Conclusions EZH2i plus Carboplatin is a promising combination treatment for AVPC.