• 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

胶质母细胞瘤肿瘤微环境的见解:当前及新兴的治疗方法

Insights into the glioblastoma tumor microenvironment: current and emerging therapeutic approaches.

作者信息

Tripathy Dev Kumar, Panda Lakshmi Priya, Biswal Suryanarayan, Barhwal Kalpana

机构信息

Department of Physiology, All India Institute of Medical Sciences (AIIMS), Bhubaneswar, India.

Department of Human Genetics and Molecular Medicine, Central University of Punjab, Bathinda, India.

出版信息

Front Pharmacol. 2024 Mar 8;15:1355242. doi: 10.3389/fphar.2024.1355242. eCollection 2024.

DOI:10.3389/fphar.2024.1355242
PMID:38523646
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10957596/
Abstract

Glioblastoma (GB) is an intrusive and recurrent primary brain tumor with low survivability. The heterogeneity of the tumor microenvironment plays a crucial role in the stemness and proliferation of GB. The tumor microenvironment induces tumor heterogeneity of cancer cells by facilitating clonal evolution and promoting multidrug resistance, leading to cancer cell progression and metastasis. It also plays an important role in angiogenesis to nourish the hypoxic tumor environment. There is a strong interaction of neoplastic cells with their surrounding microenvironment that comprise several immune and non-immune cellular components. The tumor microenvironment is a complex network of immune components like microglia, macrophages, T cells, B cells, natural killer (NK) cells, dendritic cells and myeloid-derived suppressor cells, and non-immune components such as extracellular matrix, endothelial cells, astrocytes and neurons. The prognosis of GB is thus challenging, making it a difficult target for therapeutic interventions. The current therapeutic approaches target these regulators of tumor micro-environment through both generalized and personalized approaches. The review provides a summary of important milestones in GB research, factors regulating tumor microenvironment and promoting angiogenesis and potential therapeutic agents widely used for the treatment of GB patients.

摘要

胶质母细胞瘤(GB)是一种侵袭性和复发性原发性脑肿瘤,生存率较低。肿瘤微环境的异质性在GB的干性和增殖中起着关键作用。肿瘤微环境通过促进克隆进化和多药耐药性来诱导癌细胞的肿瘤异质性,导致癌细胞进展和转移。它在血管生成中也起着重要作用,以滋养缺氧的肿瘤环境。肿瘤细胞与其周围的微环境之间存在强烈的相互作用,周围微环境由几种免疫和非免疫细胞成分组成。肿瘤微环境是一个由小胶质细胞、巨噬细胞、T细胞、B细胞、自然杀伤(NK)细胞、树突状细胞和髓源性抑制细胞等免疫成分以及细胞外基质、内皮细胞、星形胶质细胞和神经元等非免疫成分组成的复杂网络。因此,GB的预后具有挑战性,使其成为治疗干预的难题。目前的治疗方法通过通用和个性化方法针对这些肿瘤微环境调节因子。本综述总结了GB研究中的重要里程碑、调节肿瘤微环境和促进血管生成的因素以及广泛用于治疗GB患者的潜在治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ec/10957596/c2f1bd3c1c6b/fphar-15-1355242-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ec/10957596/593e51f4c4c6/fphar-15-1355242-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ec/10957596/e6f89b0e3624/fphar-15-1355242-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ec/10957596/c2f1bd3c1c6b/fphar-15-1355242-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ec/10957596/593e51f4c4c6/fphar-15-1355242-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ec/10957596/e6f89b0e3624/fphar-15-1355242-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5ec/10957596/c2f1bd3c1c6b/fphar-15-1355242-g003.jpg

相似文献

1
Insights into the glioblastoma tumor microenvironment: current and emerging therapeutic approaches.胶质母细胞瘤肿瘤微环境的见解:当前及新兴的治疗方法
Front Pharmacol. 2024 Mar 8;15:1355242. doi: 10.3389/fphar.2024.1355242. eCollection 2024.
2
Insights in the immunobiology of glioblastoma.胶质母细胞瘤的免疫生物学研究进展。
J Mol Med (Berl). 2020 Jan;98(1):1-10. doi: 10.1007/s00109-019-01835-4. Epub 2019 Oct 24.
3
CAR-Engineered NK Cells for the Treatment of Glioblastoma: Turning Innate Effectors Into Precision Tools for Cancer Immunotherapy.嵌合抗原受体修饰的自然杀伤细胞治疗胶质母细胞瘤:将固有效应细胞转化为癌症免疫治疗的精准工具。
Front Immunol. 2019 Nov 14;10:2683. doi: 10.3389/fimmu.2019.02683. eCollection 2019.
4
Single-Cell Molecular Characterization to Partition the Human Glioblastoma Tumor Microenvironment Genetic Background.单细胞分子特征分析揭示人类胶质母细胞瘤肿瘤微环境的遗传背景。
Cells. 2022 Mar 26;11(7):1127. doi: 10.3390/cells11071127.
5
NK Cell-Based Glioblastoma Immunotherapy.基于自然杀伤细胞的胶质母细胞瘤免疫疗法。
Cancers (Basel). 2018 Dec 18;10(12):522. doi: 10.3390/cancers10120522.
6
The role of vascular endothelial growth factor in the hypoxic and immunosuppressive tumor microenvironment: perspectives for therapeutic implications.血管内皮生长因子在低氧和免疫抑制性肿瘤微环境中的作用:治疗意义的展望。
Med Oncol. 2019 Nov 11;37(1):2. doi: 10.1007/s12032-019-1329-2.
7
Friends with Benefits: Chemokines, Glioblastoma-Associated Microglia/Macrophages, and Tumor Microenvironment.有共同利益的朋友:趋化因子、胶质母细胞瘤相关的小胶质细胞/巨噬细胞和肿瘤微环境。
Int J Mol Sci. 2022 Feb 24;23(5):2509. doi: 10.3390/ijms23052509.
8
Pericytes in Glioblastomas: Multifaceted Role Within Tumor Microenvironments and Potential for Therapeutic Interventions.《脑胶质瘤中的周细胞:肿瘤微环境中的多面角色和治疗干预的潜力》
Adv Exp Med Biol. 2019;1147:65-91. doi: 10.1007/978-3-030-16908-4_2.
9
Metabolic and functional reprogramming of myeloid-derived suppressor cells and their therapeutic control in glioblastoma.髓源性抑制细胞的代谢和功能重编程及其在胶质母细胞瘤中的治疗控制
Cell Stress. 2019 Jan 23;3(2):47-65. doi: 10.15698/cst2019.02.176.
10
The Complexity of the Tumor Microenvironment in Hepatocellular Carcinoma and Emerging Therapeutic Developments.肝细胞癌中肿瘤微环境的复杂性及新兴治疗进展
J Clin Med. 2023 Dec 2;12(23):7469. doi: 10.3390/jcm12237469.

引用本文的文献

1
Progenitor cells, microglia, and non-coding RNAs: Orchestrators of glioblastoma pathogenesis and therapeutic resistance.祖细胞、小胶质细胞与非编码RNA:胶质母细胞瘤发病机制及治疗耐药性的调控者
Noncoding RNA Res. 2025 Aug 5;15:85-99. doi: 10.1016/j.ncrna.2025.07.007. eCollection 2025 Dec.
2
Glioblastoma: A Multidisciplinary Approach to Its Pathophysiology, Treatment, and Innovative Therapeutic Strategies.胶质母细胞瘤:关于其病理生理学、治疗及创新治疗策略的多学科方法
Biomedicines. 2025 Aug 2;13(8):1882. doi: 10.3390/biomedicines13081882.
3
Immune factors and their role in tumor aggressiveness in glioblastoma: Atypical cadherin FAT1 as a promising target for combating immune evasion.

本文引用的文献

1
Distinct Cholesterol Localization in Glioblastoma Multiforme Revealed by Mass Spectrometry Imaging.质谱成像揭示胶质母细胞瘤中胆固醇的独特定位。
ACS Chem Neurosci. 2023 May 3;14(9):1602-1609. doi: 10.1021/acschemneuro.2c00776. Epub 2023 Apr 11.
2
Challenges in glioblastoma research: focus on the tumor microenvironment: (Trends in Cancer, 9:1 p:9-27, 2023).胶质母细胞瘤研究中的挑战:聚焦肿瘤微环境(《癌症趋势》,第9卷,第1期,第9 - 27页,2023年)
Trends Cancer. 2023 Aug;9(8):692. doi: 10.1016/j.trecan.2023.02.006. Epub 2023 Mar 28.
3
Single-cell RNA sequencing and spatial transcriptomics reveal cancer-associated fibroblasts in glioblastoma with protumoral effects.
免疫因子及其在胶质母细胞瘤肿瘤侵袭性中的作用:非典型钙黏蛋白FAT1作为对抗免疫逃逸的一个有前景的靶点。
Cell Mol Biol Lett. 2025 Jul 25;30(1):89. doi: 10.1186/s11658-025-00769-9.
4
Investigating the role of tumor cell heterogeneity and angiogenesis genes in the prognosis of multiple myeloma.探究肿瘤细胞异质性和血管生成基因在多发性骨髓瘤预后中的作用。
Front Immunol. 2025 Jun 25;16:1610833. doi: 10.3389/fimmu.2025.1610833. eCollection 2025.
5
3D Brain Vascular Niche Model Captures Glioblastoma Infiltration, Dormancy, and Gene Signatures.3D脑微血管生态位模型可捕捉胶质母细胞瘤的浸润、休眠及基因特征。
Adv Sci (Weinh). 2025 Sep;12(33):e00689. doi: 10.1002/advs.202500689. Epub 2025 Jun 19.
6
Neuro-immune crosstalk in cancer: mechanisms and therapeutic implications.癌症中的神经-免疫相互作用:机制与治疗意义
Signal Transduct Target Ther. 2025 Jun 2;10(1):176. doi: 10.1038/s41392-025-02241-8.
7
Glycosylation Gene Signatures as Prognostic Biomarkers in Glioblastoma.糖基化基因特征作为胶质母细胞瘤的预后生物标志物
Ann Clin Transl Neurol. 2025 Jul;12(7):1378-1394. doi: 10.1002/acn3.70068. Epub 2025 May 19.
8
TAMing Gliomas: Unraveling the Roles of Iba1 and CD163 in Glioblastoma.靶向胶质瘤:揭示Iba1和CD163在胶质母细胞瘤中的作用
Cancers (Basel). 2025 Apr 26;17(9):1457. doi: 10.3390/cancers17091457.
9
The function of chaperones in the radioresistance of glioblastoma: a new insight into the current knowledge.伴侣蛋白在胶质母细胞瘤放射抗性中的作用:对当前知识的新见解。
Brain Tumor Pathol. 2025 Apr 21. doi: 10.1007/s10014-025-00501-7.
10
The Effect of Ethanolic Extract of Brazilian Green Propolis and Artepillin C on Cytokine Secretion by Stage IV Glioma Cells Under Hypoxic and Normoxic Conditions.巴西绿蜂胶乙醇提取物和阿替匹林C对IV期胶质瘤细胞在缺氧和常氧条件下细胞因子分泌的影响。
Pharmaceuticals (Basel). 2025 Mar 9;18(3):389. doi: 10.3390/ph18030389.
单细胞 RNA 测序和空间转录组学揭示胶质母细胞瘤中具有促肿瘤作用的癌相关成纤维细胞。
J Clin Invest. 2023 Mar 1;133(5):e147087. doi: 10.1172/JCI147087.
4
The emerging field of oncolytic virus-based cancer immunotherapy.溶瘤病毒为基础的癌症免疫疗法的新兴领域。
Trends Cancer. 2023 Feb;9(2):122-139. doi: 10.1016/j.trecan.2022.10.003. Epub 2022 Nov 17.
5
The effect of dexamethasone on the microenvironment and efficacy of checkpoint inhibitors in glioblastoma: a systematic review.地塞米松对胶质母细胞瘤中检查点抑制剂的微环境和疗效的影响:一项系统评价
Neurooncol Adv. 2022 Jun 7;4(1):vdac087. doi: 10.1093/noajnl/vdac087. eCollection 2022 Jan-Dec.
6
Epidermal Growth Factor Receptor Variant III Mutation, an Emerging Molecular Marker in Glioblastoma Multiforme Patients: A Single Institution Study on the Indian Population.表皮生长因子受体III型突变,多形性胶质母细胞瘤患者中一种新兴的分子标志物:一项针对印度人群的单机构研究
Cureus. 2022 Jun 29;14(6):e26412. doi: 10.7759/cureus.26412. eCollection 2022 Jun.
7
NR1H3 (LXRα) is associated with pro-inflammatory macrophages, predicts survival and suggests potential therapeutic rationales in diffuse large b-cell lymphoma.NR1H3(LXRα)与促炎巨噬细胞相关,可预测弥漫性大 B 细胞淋巴瘤的生存情况,并为其提供潜在的治疗依据。
Hematol Oncol. 2022 Dec;40(5):864-875. doi: 10.1002/hon.3050. Epub 2022 Aug 9.
8
Blood-brain barrier-penetrating single CRISPR-Cas9 nanocapsules for effective and safe glioblastoma gene therapy.血脑屏障穿透型单 CRISPR-Cas9 纳米胶囊用于胶质母细胞瘤的有效和安全基因治疗。
Sci Adv. 2022 Apr 22;8(16):eabm8011. doi: 10.1126/sciadv.abm8011. Epub 2022 Apr 20.
9
Engineered Wnt ligands enable blood-brain barrier repair in neurological disorders.工程化 Wnt 配体可实现神经疾病中的血脑屏障修复。
Science. 2022 Feb 18;375(6582):eabm4459. doi: 10.1126/science.abm4459.
10
Glioma targeted therapy: insight into future of molecular approaches.脑胶质瘤靶向治疗:分子靶向治疗的未来展望。
Mol Cancer. 2022 Feb 8;21(1):39. doi: 10.1186/s12943-022-01513-z.