Wang Yufeng, Dang Huifeng, Wang Qianqian, Wu Shuxiao, Han Lei, Luo X U, Tian Yingxia, Tang Hailin
Department of Breast Medical Oncology, Affiliated Cancer Hospital of Sun Yat-sen University, Gansu Hospital, Lanzhou, 730050, China.
State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China.
Oncol Res. 2025 Jul 18;33(8):1861-1874. doi: 10.32604/or.2025.063716. eCollection 2025.
This review focuses on the metabolic issues related to mitochondrial pyruvate dehydrogenase phosphatase (PDP) in malignant tumors and its potential mechanisms. Recent research on tumor metabolic mechanisms has shown that PDP dysregulation is closely linked to metabolic reprogramming in tumor cells, and potentially promotes tumor. Research has comprehensively explored the structural-functional characteristics of PDP, its metabolic regulatory mechanisms, and its role in various types of malignant tumors. Nevertheless, several questions still exist regarding its potential mechanisms within acetylation, phosphorylation, hypoxia, immune infiltration, mitochondrial metabolism, drug resistance, oxidative phosphorylation, and tumor prognosis. This article intends to summarize the latest research, examine PDP's potential as a therapeutic target, and propose future research directions to enhance cancer treatment strategies.
本综述聚焦于恶性肿瘤中线粒体丙酮酸脱氢酶磷酸酶(PDP)相关的代谢问题及其潜在机制。近期关于肿瘤代谢机制的研究表明,PDP失调与肿瘤细胞的代谢重编程密切相关,并可能促进肿瘤发生。研究全面探讨了PDP的结构功能特征、其代谢调控机制及其在各类恶性肿瘤中的作用。然而,在乙酰化、磷酸化、缺氧、免疫浸润、线粒体代谢、耐药性、氧化磷酸化及肿瘤预后等方面,其潜在机制仍存在若干问题。本文旨在总结最新研究,审视PDP作为治疗靶点的潜力,并提出未来研究方向以加强癌症治疗策略。