Malonyl-CoA Promotes Prostate Cancer Progression and Castration Resistance by Enhancing Lipogenesis and Ran Activation

Abstract

Malonyl-CoA, a key metabolite, is not only the building block for lipogenesis, but also a critical regulator of mitochondrial fatty acid (FA) β-oxidation. Given the altered metabolic state of many cancers, malonyl-CoA may play a role in tumor development and drug resistance, especially in malignancies characterized by abnormal lipid metabolism, such as prostate cancer (PCa). Here, we showed that the levels of malonyl-CoA were increased in PCa, especially in castration-resistant prostate cancer (CRPC). Abnormal accumulation of malonyl-CoA promoted lipogenesis and regulated metabolic processes, maintaining endoplasmic reticulum (ER) homeostasis and mitochondrial function and ultimately contributing to PCa progression. Restoration of malonyl-CoA decarboxylase (MLYCD) expression activated the unfolded protein response via the consumption of malonyl-CoA. Importantly, malonyl-CoA accumulation promoted lysine malonylation in PCa. Ran K141 malonylation increased Ran activity and enhanced androgen receptor nuclear translocation and transcriptional activity, ultimately contributing to PCa development and resistance to antiandrogens. These findings highlight the function of malonyl-CoA in PCa progression by regulating metabolic processes and malonylating Ran K141, revealing that the malonyl-CoA axis might be a reliable biomarker and a potential therapeutic target in PCa.