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膀胱癌免疫治疗中靶向代谢重编程:一种精准医学方法。

Targeting Metabolic Reprogramming in Bladder Cancer Immunotherapy: A Precision Medicine Approach.

作者信息

Liu Fuyang, Li Kai, Zhu Qingyi

机构信息

Department of Urology, The Second Affiliated Hospital of Nanjing Medical University, Nanjing 210011, China.

出版信息

Biomedicines. 2025 May 9;13(5):1145. doi: 10.3390/biomedicines13051145.

DOI:10.3390/biomedicines13051145
PMID:40426972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12108893/
Abstract

Bladder cancer, as a highly heterogeneous malignant tumor of the urinary system, is significantly affected by tumor metabolic reprogramming in its response to immunotherapy. This review systematically elaborates on the molecular mechanisms of abnormal glucose and lipid metabolism in the bladder cancer microenvironment and immune escape, and discusses precision treatment strategies based on metabolic regulation. In the future, it will be necessary to combine spatiotemporal omics and artificial intelligence technologies to construct a multi-target intervention system for the metabolic-immune interaction network, promoting a paradigm shift in precision treatment for bladder cancer.

摘要

膀胱癌作为泌尿系统一种高度异质性的恶性肿瘤,在其对免疫治疗的反应中受到肿瘤代谢重编程的显著影响。本文综述系统阐述了膀胱癌微环境中糖脂代谢异常及免疫逃逸的分子机制,并探讨了基于代谢调控的精准治疗策略。未来,有必要结合时空组学和人工智能技术,构建代谢-免疫相互作用网络的多靶点干预体系,推动膀胱癌精准治疗的模式转变。

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本文引用的文献

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Advancements in the Diagnosis, Treatment, and Risk Stratification of Non-Muscle Invasive Bladder Cancer.非肌层浸润性膀胱癌的诊断、治疗及风险分层进展
Curr Oncol Rep. 2025 Mar;27(3):236-246. doi: 10.1007/s11912-025-01645-7. Epub 2025 Feb 20.
2
Targeting the PD-1/PD-L1 Signaling Pathway for Cancer Therapy: Focus on Biomarkers.靶向PD-1/PD-L1信号通路用于癌症治疗:聚焦生物标志物。
Int J Mol Sci. 2025 Jan 31;26(3):1235. doi: 10.3390/ijms26031235.
3
State of the art of adjuvant immunotherapy in urothelial cancer: New developments and upcoming changes.
尿路上皮癌辅助免疫治疗的现状:新进展与即将到来的变化
Hum Vaccin Immunother. 2025 Dec;21(1):2440165. doi: 10.1080/21645515.2024.2440165. Epub 2024 Dec 19.
4
CircZNF609 inhibited bladder cancer immunotherapy sensitivity via enhancing fatty acid uptake through IGF2BP2/CD36 pathway.环状锌指蛋白 609 通过 IGF2BP2/CD36 通路增强脂肪酸摄取来抑制膀胱癌免疫治疗敏感性。
Int Immunopharmacol. 2024 Aug 20;137:112485. doi: 10.1016/j.intimp.2024.112485. Epub 2024 Jun 14.
5
Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.2022 年全球癌症统计数据:全球 185 个国家和地区 36 种癌症的发病率和死亡率全球估计数。
CA Cancer J Clin. 2024 May-Jun;74(3):229-263. doi: 10.3322/caac.21834. Epub 2024 Apr 4.
6
Metabolic reprogramming based on RNA sequencing of gemcitabine-resistant cells reveals the FASN gene as a therapeutic for bladder cancer.基于吉西他滨耐药细胞的 RNA 测序的代谢重编程揭示 FASN 基因是膀胱癌的一种治疗方法。
J Transl Med. 2024 Jan 13;22(1):55. doi: 10.1186/s12967-024-04867-8.
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Acyl-coenzyme A: cholesterol acyltransferase inhibitor avasimibe suppresses tumorigenesis and induces G1-phase cell-cycle arrest by activating PPARγ signaling pathway in bladder cancer.酰基辅酶A:胆固醇酰基转移酶抑制剂阿伐西丁通过激活膀胱癌中的PPARγ信号通路抑制肿瘤发生并诱导G1期细胞周期停滞。
J Cancer. 2024 Jan 1;15(2):370-382. doi: 10.7150/jca.83856. eCollection 2024.
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Cell cycle arrest induces lipid droplet formation and confers ferroptosis resistance.细胞周期停滞诱导脂滴形成并赋予铁死亡抗性。
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Lipidomics Profiling Reveals Differential Alterations after FAS Inhibition in 3D Colon Cancer Cell Culture Models.脂质组学分析揭示了 FAS 抑制在 3D 结肠癌细胞培养模型中的差异变化。
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