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靶向肠道微生物群:胶质瘤肿瘤微环境的一种潜在治疗方法。

Targeting gut microbiota: a potential therapeutic approach for tumor microenvironment in glioma.

作者信息

Qi Fan, Meng Kaiqiang, Zhao Xiaoping, Lv Jing, Huang Lan, Fan Xiaoxuan, Feng Zhaoqun

机构信息

College of Integrated Traditional and Western Medicine, Shaanxi University of Chinese Medicine, Shaanxi, China.

College of Traditional Chinese Medicine, Shaanxi University of Chinese Medicine, Shaanxi, China.

出版信息

Front Neurol. 2025 Mar 21;16:1549465. doi: 10.3389/fneur.2025.1549465. eCollection 2025.

DOI:10.3389/fneur.2025.1549465
PMID:40183013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11965986/
Abstract

Glioma, being one of the malignant tumors with the highest mortality rate globally, has an unclear pathogenesis, and the existing treatment effects still have certain limitations. The tumor microenvironment (TME) plays an important role in the occurrence, development, and recurrence of glioma. As one of the important regulatory factors of TME, the gut microbiota can regulate the progression of glioma not only by interacting with the brain through the brain-gut axis but also by influencing the tumor immune microenvironment (TIME) and inflammatory microenvironment. Recent studies have identified the gut microbiota and TME as potential therapeutic targets for glioma. This paper aims to summarize the role of the gut microbiota in TME, the association between them and glioma, and the potential of developing new intervention measures by targeting the gut microbiota. Understanding the involvement process of the gut microbiota in glioma may pave the way for the development of effective treatment methods that can regulate TME and prevent disease progression.

摘要

胶质瘤是全球死亡率最高的恶性肿瘤之一,其发病机制尚不清楚,现有治疗效果仍存在一定局限性。肿瘤微环境(TME)在胶质瘤的发生、发展和复发中起重要作用。作为TME的重要调节因子之一,肠道微生物群不仅可以通过脑-肠轴与大脑相互作用,还可以通过影响肿瘤免疫微环境(TIME)和炎症微环境来调节胶质瘤的进展。最近的研究已将肠道微生物群和TME确定为胶质瘤的潜在治疗靶点。本文旨在总结肠道微生物群在TME中的作用、它们与胶质瘤之间的关联以及通过靶向肠道微生物群开发新干预措施的潜力。了解肠道微生物群在胶质瘤中的参与过程可能为开发能够调节TME并预防疾病进展的有效治疗方法铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b12/11965986/ffeb150879c1/fneur-16-1549465-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b12/11965986/a5f46d40c4ff/fneur-16-1549465-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b12/11965986/ffeb150879c1/fneur-16-1549465-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b12/11965986/a5f46d40c4ff/fneur-16-1549465-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b12/11965986/ffeb150879c1/fneur-16-1549465-g002.jpg

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本文引用的文献

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Intestinal Bacteroides drives glioma progression by regulating CD8+ T cell tumor infiltration.肠道拟杆菌通过调节CD8+T细胞肿瘤浸润驱动胶质瘤进展。
Neuro Oncol. 2025 Jan 27. doi: 10.1093/neuonc/noaf024.
2
Multi-omics analysis reveals the interplay between intratumoral bacteria and glioma.多组学分析揭示了肿瘤内细菌与神经胶质瘤之间的相互作用。
mSystems. 2025 Jan 21;10(1):e0045724. doi: 10.1128/msystems.00457-24. Epub 2024 Dec 11.
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Short-chain fatty acids reverses gut microbiota dysbiosis-promoted progression of glioblastoma by up-regulating M1 polarization in the tumor microenvironment.
短链脂肪酸通过上调肿瘤微环境中 M1 极化逆转肠道菌群失调促进胶质母细胞瘤的进展。
Int Immunopharmacol. 2024 Nov 15;141:112881. doi: 10.1016/j.intimp.2024.112881. Epub 2024 Aug 18.
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Relevance of harmful intratumoral microbiota in cancer progression and its clinical application.肿瘤内有害微生物组在癌症进展中的相关性及其临床应用。
Biomed Pharmacother. 2024 Sep;178:117238. doi: 10.1016/j.biopha.2024.117238. Epub 2024 Aug 5.
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Exosomal TNF-α mediates voltage-gated Na+ channel 1.6 overexpression and contributes to brain tumor-induced neuronal hyperexcitability.外泌体 TNF-α 介导线电压门控 Na+ 通道 1.6 的过表达,并有助于脑肿瘤引起的神经元过度兴奋。
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Histone serotonylation regulates ependymoma tumorigenesis.组蛋白 5-羟色胺酰化调控室管膜瘤发生。
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7
IL-13Rα2/TGF-β bispecific CAR-T cells counter TGF-β-mediated immune suppression and potentiate anti-tumor responses in glioblastoma.IL-13Rα2/TGF-β 双特异性 CAR-T 细胞可克服 TGF-β 介导的免疫抑制,增强胶质母细胞瘤的抗肿瘤反应。
Neuro Oncol. 2024 Oct 3;26(10):1850-1866. doi: 10.1093/neuonc/noae126.
8
Role of gut microbiota in regulating immune checkpoint inhibitor therapy for glioblastoma.肠道微生物群在调控胶质母细胞瘤免疫检查点抑制剂治疗中的作用。
Front Immunol. 2024 Jun 10;15:1401967. doi: 10.3389/fimmu.2024.1401967. eCollection 2024.
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Understanding the immunosuppressive microenvironment of glioma: mechanistic insights and clinical perspectives.了解胶质瘤的免疫抑制微环境:机制见解和临床观点。
J Hematol Oncol. 2024 May 8;17(1):31. doi: 10.1186/s13045-024-01544-7.
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J Immunother Cancer. 2024 Apr 9;12(4):e008880. doi: 10.1136/jitc-2024-008880.