Jiang Haoran, Zeng Yuan, Ning Weiqiang, Hong Junkai, Zhu Moyang, Li Ping, Ye Fangdie, Chen Zhifa, Chen Haoran, Chen Wei, Li Gang, Huang Hang
Department of Urology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China; Institute of Urology, Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China; Zhejiang Key Laboratory of Critical Care Medicine,Wenzhou, 325000,Zhejiang China; Translational Medicine Laboratory, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China; Key Laboratory of Novel Nuclide Technologies on Precision Diagnosis and Treatment & Clinical Transformation of Wenzhou City, Wenzhou, 325035, Zhejiang, China; Department of Radiation Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China.
Department of Gastroenterology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325035, Zhejiang, China.
Cancer Lett. 2025 Aug 10;625:217808. doi: 10.1016/j.canlet.2025.217808. Epub 2025 May 18.
Next-generation androgen receptor inhibitors are the primary treatment for metastatic prostate cancer. Unfortunately, the majority of patients rapidly develop resistance. Resistance to enzalutamide has been linked to the emergence of an immunosuppressive tumor, although the underlying mechanisms remain poorly understood. In this study, we observed a marked overexpression of enzymes involved in the ketogenic pathway in enzalutamide-induced castration-resistant prostate cancer, which contributed to immune desertification and resistance to immunotherapy. Mechanistically, upregulation of the ketogenic pathway led to the accumulation of β-hydroxybutyrate, which promoted β-hydroxybutyrylation of the cell cycle-regulated deubiquitinase OTUD7B at lysine 511. This modification impaired the degradation of APC/C substrates, resulting in a subsequent reduction in cytoplasmic double-stranded DNA accumulation, thereby attenuating cGAS-STING activation and interferon expression. These findings shed light on the metabolic adaptations and immune escape driven by androgen receptor signaling inhibitors, potentially informing the development of more effective and durable therapeutic approaches in the near future.
新一代雄激素受体抑制剂是转移性前列腺癌的主要治疗方法。不幸的是,大多数患者会迅速产生耐药性。恩杂鲁胺耐药与免疫抑制性肿瘤的出现有关,但其潜在机制仍知之甚少。在本研究中,我们观察到在恩杂鲁胺诱导的去势抵抗性前列腺癌中,参与生酮途径的酶显著过表达,这导致了免疫沙漠化和对免疫治疗的抵抗。从机制上讲,生酮途径的上调导致β-羟基丁酸的积累,后者促进细胞周期调节的去泛素化酶OTUD7B在赖氨酸511处的β-羟基丁酰化。这种修饰损害了后期促进复合物/细胞周期体(APC/C)底物的降解,导致随后细胞质双链DNA积累减少,从而减弱cGAS-STING激活和干扰素表达。这些发现揭示了雄激素受体信号抑制剂驱动的代谢适应和免疫逃逸,可能为在不久的将来开发更有效和持久的治疗方法提供信息。