• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

脑肿瘤微环境中的老明星与新角色

Old Stars and New Players in the Brain Tumor Microenvironment.

作者信息

Parmigiani Elena, Scalera Marta, Mori Elisabetta, Tantillo Elena, Vannini Eleonora

机构信息

Embryology and Stem Cell Biology, Department of Biomedicine, University of Basel, Basel, Switzerland.

Neuroscience Institute, Consiglio Nazionale delle Ricerche (CNR), Pisa, Italy.

出版信息

Front Cell Neurosci. 2021 Oct 6;15:709917. doi: 10.3389/fncel.2021.709917. eCollection 2021.

DOI:10.3389/fncel.2021.709917
PMID:34690699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8527006/
Abstract

In recent years, the direct interaction between cancer cells and tumor microenvironment (TME) has emerged as a crucial regulator of tumor growth and a promising therapeutic target. The TME, including the surrounding peritumoral regions, is dynamically modified during tumor progression and in response to therapies. However, the mechanisms regulating the crosstalk between malignant and non-malignant cells are still poorly understood, especially in the case of glioma, an aggressive form of brain tumor. The presence of unique brain-resident cell types, namely neurons and glial cells, and an exceptionally immunosuppressive microenvironment pose additional important challenges to the development of effective treatments targeting the TME. In this review, we provide an overview on the direct and indirect interplay between glioma and neuronal and glial cells, introducing new players and mechanisms that still deserve further investigation. We will focus on the effects of neural activity and glial response in controlling glioma cell behavior and discuss the potential of exploiting these cellular interactions to develop new therapeutic approaches with the aim to preserve proper brain functionality.

摘要

近年来,癌细胞与肿瘤微环境(TME)之间的直接相互作用已成为肿瘤生长的关键调节因子和一个有前景的治疗靶点。肿瘤微环境包括周围的肿瘤周围区域,在肿瘤进展过程中以及对治疗的反应中会动态改变。然而,调节恶性细胞与非恶性细胞之间串扰的机制仍知之甚少,尤其是在胶质瘤这种侵袭性脑肿瘤的情况下。独特的脑驻留细胞类型,即神经元和神经胶质细胞的存在,以及异常免疫抑制的微环境,给开发针对肿瘤微环境的有效治疗方法带来了额外的重大挑战。在这篇综述中,我们概述了胶质瘤与神经元和神经胶质细胞之间的直接和间接相互作用,介绍了仍值得进一步研究的新参与者和机制。我们将重点关注神经活动和神经胶质反应在控制胶质瘤细胞行为方面的作用,并讨论利用这些细胞相互作用开发新治疗方法以保留适当脑功能的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86eb/8527006/6a6740dcb582/fncel-15-709917-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86eb/8527006/6a6740dcb582/fncel-15-709917-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86eb/8527006/6a6740dcb582/fncel-15-709917-g001.jpg

相似文献

1
Old Stars and New Players in the Brain Tumor Microenvironment.脑肿瘤微环境中的老明星与新角色
Front Cell Neurosci. 2021 Oct 6;15:709917. doi: 10.3389/fncel.2021.709917. eCollection 2021.
2
Glioma-associated microglia/macrophages (GAMs) in glioblastoma: Immune function in the tumor microenvironment and implications for immunotherapy.胶质母细胞瘤相关的小胶质细胞/巨噬细胞(GAMs):肿瘤微环境中的免疫功能及其对免疫治疗的影响。
Front Immunol. 2023 Mar 9;14:1123853. doi: 10.3389/fimmu.2023.1123853. eCollection 2023.
3
Glioma-Associated Microglia Characterization in the Glioblastoma Microenvironment through a 'Seed-and Soil' Approach: A Systematic Review.通过“种子与土壤”方法对胶质母细胞瘤微环境中胶质瘤相关小胶质细胞的特征进行系统评价
Brain Sci. 2022 May 31;12(6):718. doi: 10.3390/brainsci12060718.
4
Microglia and Brain Macrophages as Drivers of Glioma Progression.小胶质细胞和脑巨噬细胞作为胶质瘤进展的驱动因素。
Int J Mol Sci. 2022 Dec 9;23(24):15612. doi: 10.3390/ijms232415612.
5
Role of myeloid cells in the immunosuppressive microenvironment in gliomas.髓系细胞在胶质瘤免疫抑制微环境中的作用。
Immunobiology. 2020 Jan;225(1):151853. doi: 10.1016/j.imbio.2019.10.002. Epub 2019 Oct 19.
6
Current perspectives on diffuse midline glioma and a different role for the immune microenvironment compared to glioblastoma.目前对弥漫性中线胶质瘤的看法,以及与胶质母细胞瘤相比,其免疫微环境的不同作用。
J Neuroinflammation. 2022 Nov 19;19(1):276. doi: 10.1186/s12974-022-02630-8.
7
When Immune Cells Turn Bad-Tumor-Associated Microglia/Macrophages in Glioma.当免疫细胞“叛变”——胶质瘤中的肿瘤相关小胶质细胞/巨噬细胞。
Int J Mol Sci. 2018 Feb 1;19(2):436. doi: 10.3390/ijms19020436.
8
Co-culture models for investigating cellular crosstalk in the glioma microenvironment.用于研究胶质瘤微环境中细胞间相互作用的共培养模型。
Cancer Pathog Ther. 2023 Nov 7;2(4):219-230. doi: 10.1016/j.cpt.2023.11.002. eCollection 2024 Oct.
9
Exploring Monocytes-Macrophages in Immune Microenvironment of Glioblastoma for the Design of Novel Therapeutic Strategies.探索胶质母细胞瘤免疫微环境中的单核细胞-巨噬细胞以设计新型治疗策略。
Brain Sci. 2023 Mar 24;13(4):542. doi: 10.3390/brainsci13040542.
10
[Latest Research Findings on the Role of Non-Tumor Cells in Glioma Microenvironment].[胶质瘤微环境中非肿瘤细胞作用的最新研究发现]
Sichuan Da Xue Xue Bao Yi Xue Ban. 2022 Jul;53(4):573-578. doi: 10.12182/20220760204.

引用本文的文献

1
Connexin hemichannel blockade by abEC1.1 disrupts glioblastoma progression, suppresses invasiveness, and reduces hyperexcitability in preclinical models.abEC1.1对连接蛋白半通道的阻断可破坏胶质母细胞瘤的进展,抑制侵袭性,并降低临床前模型中的过度兴奋性。
Cell Commun Signal. 2025 Sep 2;23(1):391. doi: 10.1186/s12964-025-02370-1.
2
Interrogation of macrophage-related prognostic signatures reveals a potential immune-mediated therapy strategy by histone deacetylase inhibition in glioma.对巨噬细胞相关预后特征的研究揭示了一种通过抑制组蛋白去乙酰化酶在胶质瘤中进行潜在免疫介导治疗的策略。
Front Oncol. 2025 Jun 6;15:1554845. doi: 10.3389/fonc.2025.1554845. eCollection 2025.
3

本文引用的文献

1
The white matter is a pro-differentiative niche for glioblastoma.白质是胶质母细胞瘤的促分化龛位。
Nat Commun. 2021 Apr 12;12(1):2184. doi: 10.1038/s41467-021-22225-w.
2
Single-cell profiling of myeloid cells in glioblastoma across species and disease stage reveals macrophage competition and specialization.跨物种和疾病阶段对胶质母细胞瘤中髓样细胞进行单细胞分析揭示了巨噬细胞的竞争和特化。
Nat Neurosci. 2021 Apr;24(4):595-610. doi: 10.1038/s41593-020-00789-y. Epub 2021 Mar 29.
3
Multiple sclerosis risk gene Mertk is required for microglial activation and subsequent remyelination.
Chimeric antigen receptor-macrophages: Emerging next-generation cell therapy for brain cancer.
嵌合抗原受体巨噬细胞:新兴的脑癌下一代细胞疗法。
Neurooncol Adv. 2025 Mar 19;7(1):vdaf059. doi: 10.1093/noajnl/vdaf059. eCollection 2025 Jan-Dec.
4
Polycystins Expression in Astrocytic Gliomas.多囊蛋白在星形胶质细胞瘤中的表达
Biomedicines. 2025 Apr 5;13(4):884. doi: 10.3390/biomedicines13040884.
5
Advances in bioengineered CAR T/NK cell therapy for glioblastoma: Overcoming immunosuppression and nanotechnology-based strategies for enhanced CAR T/NK cell therapy.用于胶质母细胞瘤的生物工程化嵌合抗原受体T细胞/自然杀伤细胞疗法的进展:克服免疫抑制及基于纳米技术增强嵌合抗原受体T细胞/自然杀伤细胞疗法的策略
Bioeng Transl Med. 2024 Aug 31;10(2):e10716. doi: 10.1002/btm2.10716. eCollection 2025 Mar.
6
Peritumoral Brain Zone in Astrocytoma: Morphology, Molecular Aspects, and Clinical Manifestations (Review).脑胶质瘤瘤周区:形态学、分子学方面和临床表现(综述)。
Sovrem Tekhnologii Med. 2024;16(2):79-88. doi: 10.17691/stm2024.16.2.08. Epub 2024 Apr 27.
7
A Photopolymerizable Hyaluronic Acid-Collagen Model of the Invasive Glioma Microenvironment with Interstitial Flow.具有间质流的光聚合透明质酸-胶原侵袭性神经胶质瘤微环境模型。
J Vis Exp. 2024 Oct 18(212). doi: 10.3791/66604.
8
Glioma-Stem-Cell-Derived Exosomes Remodeled Glioma-Associated Macrophage via NEAT1/miR-125a/STAT3 Pathway.胶质瘤干细胞衍生的外泌体通过NEAT1/miR-125a/STAT3途径重塑胶质瘤相关巨噬细胞
Cancers (Basel). 2024 Jul 9;16(14):2500. doi: 10.3390/cancers16142500.
9
Non-Tumor Cells within the Tumor Microenvironment-The "Eminence Grise" of the Glioblastoma Pathogenesis and Potential Targets for Therapy.肿瘤微环境中的非肿瘤细胞——胶质母细胞瘤发病机制中的“幕后黑手”和潜在治疗靶点。
Cells. 2024 May 9;13(10):808. doi: 10.3390/cells13100808.
10
Exosomal non-coding RNAs in glioma progression: insights into tumor microenvironment dynamics and therapeutic implications.胶质瘤进展中的外泌体非编码RNA:对肿瘤微环境动态变化及治疗意义的见解
Front Cell Dev Biol. 2023 Nov 1;11:1275755. doi: 10.3389/fcell.2023.1275755. eCollection 2023.
多发性硬化症风险基因 Mertk 对于小胶质细胞的激活和随后的髓鞘再生是必需的。
Cell Rep. 2021 Mar 9;34(10):108835. doi: 10.1016/j.celrep.2021.108835.
4
Microglia in Cancer Therapy-Related Cognitive Impairment.小胶质细胞在癌症治疗相关认知障碍中的作用。
Trends Neurosci. 2021 Jun;44(6):441-451. doi: 10.1016/j.tins.2021.02.003. Epub 2021 Mar 2.
5
Single-cell RNA sequencing reveals functional heterogeneity of glioma-associated brain macrophages.单细胞 RNA 测序揭示了胶质瘤相关脑巨噬细胞的功能异质性。
Nat Commun. 2021 Feb 19;12(1):1151. doi: 10.1038/s41467-021-21407-w.
6
The immune-inflammatory response of oligodendrocytes in a murine model of preterm white matter injury: the role of TLR3 activation.早产儿脑白质损伤模型中少突胶质细胞的免疫炎症反应:TLR3 激活的作用。
Cell Death Dis. 2021 Feb 8;12(2):166. doi: 10.1038/s41419-021-03446-9.
7
High-throughput phenotypic screen and transcriptional analysis identify new compounds and targets for macrophage reprogramming.高通量表型筛选和转录分析鉴定用于巨噬细胞重编程的新化合物和靶标。
Nat Commun. 2021 Feb 3;12(1):773. doi: 10.1038/s41467-021-21066-x.
8
Insulin signaling mediates neurodegeneration in glioma.胰岛素信号转导介导神经胶质瘤中的神经退行性变。
Life Sci Alliance. 2021 Feb 1;4(3). doi: 10.26508/lsa.202000693. Print 2021 Mar.
9
The Irradiated Brain Microenvironment Supports Glioma Stemness and Survival via Astrocyte-Derived Transglutaminase 2.辐照后的脑微环境通过星形胶质细胞衍生的转谷氨酰胺酶 2 支持神经胶质瘤干细胞特性和存活。
Cancer Res. 2021 Apr 15;81(8):2101-2115. doi: 10.1158/0008-5472.CAN-20-1785. Epub 2021 Jan 22.
10
Interactions between Tumor Cells, Neurons, and Microglia in the Glioma Microenvironment.肿瘤细胞、神经元和小胶质细胞在神经胶质瘤微环境中的相互作用。
Int J Mol Sci. 2020 Nov 11;21(22):8476. doi: 10.3390/ijms21228476.