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结直肠癌中的线粒体代谢重编程:耐药机制与未来临床干预措施

Mitochondrial metabolic reprogramming in colorectal cancer: mechanisms of resistance and future clinical interventions.

作者信息

Qiu Xiuxiu, Wang Ao, Wang Jiahui, Zhang Zhanxia, Tao Li

机构信息

Department of Oncology, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Department of Nephrology, Yueyang Integrated Traditional Chinese and Western Medicine Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

Cell Death Discov. 2025 Aug 9;11(1):375. doi: 10.1038/s41420-025-02670-y.

Abstract

Colorectal cancer (CRC) is a leading cause of global cancer mortality, with therapeutic resistance constituting a major barrier to sustained clinical benefit. Mitochondrial metabolic reprogramming has emerged as a central adaptive mechanism that enables CRC cells to withstand hypoxia and therapeutic pressure, while concurrently driving resistance to chemotherapy, targeted agents, and immunotherapy. In this Review, we explore how mitochondrial metabolism contributes to therapeutic resistance, with particular emphasis on metabolic plasticity, redox balance, and organelle quality control. We also assess enabling technologies such as spatial transcriptomics, proteomics, and patient-derived organoids, and discuss their translational relevance in stratifying metabolic vulnerabilities and informing individualized therapies. Targeting mitochondrial rewiring represents a compelling strategy to overcome resistance and drive progress toward personalized CRC therapy.

摘要

结直肠癌(CRC)是全球癌症死亡的主要原因,治疗耐药性是持续获得临床益处的主要障碍。线粒体代谢重编程已成为一种核心适应性机制,使CRC细胞能够耐受缺氧和治疗压力,同时导致对化疗、靶向药物和免疫疗法产生耐药性。在本综述中,我们探讨线粒体代谢如何导致治疗耐药性,特别强调代谢可塑性、氧化还原平衡和细胞器质量控制。我们还评估了空间转录组学、蛋白质组学和患者来源的类器官等支持技术,并讨论它们在分层代谢脆弱性和指导个体化治疗方面的转化相关性。靶向线粒体重塑是克服耐药性并推动个性化CRC治疗取得进展的一种有吸引力的策略。

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