Pardella Elisa, Comito Giuseppina, Ippolito Luigi, Pranzini Erica, Iozzo Marta, Gangarossa Giulia, Virgilio Francesca, Bua Silvia, Nocentini Alessio, Sandrini Giada, Lorito Nicla, Bacci Marina, Nesi Gabriella, Spatafora Pietro, Serni Sergio, Supuran Claudiu T, Morandi Andrea, Chiarugi Paola, Giannoni Elisa
Department of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, Italy.
Department of NEUROFARBA, Pharmaceutical and Nutraceutical Section, University of Florence, Italy.
Mol Oncol. 2025 Sep;19(9):2515-2536. doi: 10.1002/1878-0261.70083. Epub 2025 Jun 26.
Ferroptosis is a form of regulated cell death dependent on iron-driven phospholipid peroxidation and is controlled by both cell autonomous and non-cell autonomous mechanisms. In prostate cancer (PCa), tumor cells engage in a metabolic crosstalk with cancer-associated fibroblasts (CAFs), resulting in increased utilization of CAF-secreted lactic acid, that ultimately supports cancer aggressiveness. In this context, the effect of the prostate tumor microenvironment in modulating ferroptosis sensitivity has not yet been extensively investigated. Here, we demonstrate that CAF-secreted lactic acid protects PCa cells from ferroptosis induction and supports the upregulation of the antioxidant enzyme glutathione peroxidase 4 (GPX4). Interestingly, targeting carbonic anhydrase IX/XII (CA IX/XII), the main regulators of microenvironmental acidosis, in tumor and stromal compartments hinders lactic acid shuttle within the tumor-stroma interplay and thus, prevents ferroptosis resistance induced by lactic acid. Analyses of tissue samples from PCa patients also revealed that GPX4, CA IX, and CA XII expression levels increase during PCa progression. Overall, these findings support a role for stromal lactic acid in mediating ferroptosis resistance in PCa, identifying CA IX/XII as potential therapeutic targets regulating ferroptosis sensitivity.
铁死亡是一种依赖铁驱动的磷脂过氧化作用的程序性细胞死亡形式,受细胞自主和非细胞自主机制的控制。在前列腺癌(PCa)中,肿瘤细胞与癌症相关成纤维细胞(CAF)发生代谢串扰,导致对CAF分泌的乳酸利用增加,这最终促进了癌症的侵袭性。在这种情况下,前列腺肿瘤微环境对铁死亡敏感性的调节作用尚未得到广泛研究。在此,我们证明CAF分泌的乳酸可保护PCa细胞免受铁死亡诱导,并支持抗氧化酶谷胱甘肽过氧化物酶4(GPX4)的上调。有趣的是,靶向肿瘤和基质区室中微环境酸中毒的主要调节因子碳酸酐酶IX/XII(CA IX/XII),会阻碍肿瘤-基质相互作用中的乳酸穿梭,从而防止乳酸诱导的铁死亡抗性。对PCa患者组织样本的分析还显示,在PCa进展过程中,GPX4、CA IX和CA XII的表达水平会升高。总体而言,这些发现支持基质乳酸在介导PCa铁死亡抗性中的作用,将CA IX/XII确定为调节铁死亡敏感性的潜在治疗靶点。