• 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

单细胞转录组特征分析与胶质母细胞瘤相关的小胶质细胞改变 小胶质细胞对肿瘤形成的贡献。

Single-Cell Transcriptome Profiling Signatures and Alterations of Microglia Associated With Glioblastoma Associate Microglia Contribution to Tumor Formation.

机构信息

Department of Neurosurgery, Chongqing Red Cross Hospital (Jiangbei District People's Hospital), Chongqing, China.

Department of Neurosurgery, Bishan District People's Hospital, Chongqing, China.

出版信息

Pathol Oncol Res. 2022 May 25;28:1610067. doi: 10.3389/pore.2022.1610067. eCollection 2022.

DOI:10.3389/pore.2022.1610067
PMID:35693633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9176381/
Abstract

Glioblastoma (GBM), which occasionally occurs in pediatric patients, is the most common tumor of the central nervous system in adults. Clinically, GBM is classified as low-grade to high-grade (from 1 to 4) and is characterized by late discovery, limited effective treatment methods, and poor efficacy. With the development of immunotherapy technology, effective GBM treatment strategies are of great significance. The main immune cells found in the GBM tumor microenvironment are macrophages and microglia (MG). Both these monocytes play important roles in the occurrence and development of GBM. Macrophages are recruited during tumorigenesis, whereas MG is present in the brain during embryonic development. Interestingly, the accumulation of these monocytes is inversely proportional to the survival of adult GBM patients but not the pediatric GBM patients. This study used single-cell RNA-seq data to reveal the heterogeneity of MG in tumor lesions and to explore the role of different MG subtypes in the occurrence and development of GBM. The results may help find new targets for immunotherapy of GBM.

摘要

胶质母细胞瘤(GBM)偶尔发生于儿科患者,是成人中枢神经系统最常见的肿瘤。临床上,GBM 分为低级别到高级别(1 级到 4 级),其特征为发现较晚、有效治疗方法有限、疗效不佳。随着免疫治疗技术的发展,有效的 GBM 治疗策略具有重要意义。GBM 肿瘤微环境中的主要免疫细胞是巨噬细胞和小胶质细胞(MG)。这两种单核细胞在 GBM 的发生和发展中都发挥着重要作用。巨噬细胞在肿瘤发生时被募集,而 MG 则存在于胚胎发育的大脑中。有趣的是,这些单核细胞的积累与成人 GBM 患者的存活率成反比,但与儿科 GBM 患者无关。本研究使用单细胞 RNA-seq 数据揭示了肿瘤病变中 MG 的异质性,并探讨了不同 MG 亚型在 GBM 发生和发展中的作用。研究结果可能有助于为 GBM 的免疫治疗寻找新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/ca6b400501a8/pore-28-1610067-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/b68f72c0277a/pore-28-1610067-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/ad24b2216105/pore-28-1610067-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/b90e06dbcd80/pore-28-1610067-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/0ebd17890bd8/pore-28-1610067-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/ca6b400501a8/pore-28-1610067-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/b68f72c0277a/pore-28-1610067-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/ad24b2216105/pore-28-1610067-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/b90e06dbcd80/pore-28-1610067-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/0ebd17890bd8/pore-28-1610067-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39c/9176381/ca6b400501a8/pore-28-1610067-g005.jpg

相似文献

1
Single-Cell Transcriptome Profiling Signatures and Alterations of Microglia Associated With Glioblastoma Associate Microglia Contribution to Tumor Formation.单细胞转录组特征分析与胶质母细胞瘤相关的小胶质细胞改变 小胶质细胞对肿瘤形成的贡献。
Pathol Oncol Res. 2022 May 25;28:1610067. doi: 10.3389/pore.2022.1610067. eCollection 2022.
2
Loss of CX3CR1 increases accumulation of inflammatory monocytes and promotes gliomagenesis.CX3CR1的缺失会增加炎性单核细胞的积累并促进胶质瘤的发生。
Oncotarget. 2015 Jun 20;6(17):15077-94. doi: 10.18632/oncotarget.3730.
3
Exploring the prognostic value of BRMS1 + microglia based on single-cell anoikis regulator patterns in the immunologic microenvironment of GBM.基于单细胞失巢凋亡调节因子模式探索BRMS1 +小胶质细胞在胶质母细胞瘤免疫微环境中的预后价值。
J Neurooncol. 2024 Oct;170(1):101-117. doi: 10.1007/s11060-024-04781-5. Epub 2024 Aug 15.
4
Microglia/macrophages express alternative proangiogenic factors depending on granulocyte content in human glioblastoma.小胶质细胞/巨噬细胞根据人胶质母细胞瘤中的粒细胞含量表达替代的促血管生成因子。
J Pathol. 2021 Feb;253(2):160-173. doi: 10.1002/path.5569. Epub 2020 Nov 24.
5
Integrative analysis of single-cell transcriptomics reveals age-associated immune landscape of glioblastoma.单细胞转录组学的综合分析揭示胶质母细胞瘤与年龄相关的免疫景观。
Front Immunol. 2023 Jan 24;14:1028775. doi: 10.3389/fimmu.2023.1028775. eCollection 2023.
6
Molecular profiling of the tumor microenvironment in glioblastoma patients: correlation of microglia/macrophage polarization state with metalloprotease expression profiles and survival.胶质母细胞瘤患者肿瘤微环境的分子剖析:小胶质细胞/巨噬细胞极化状态与金属蛋白酶表达谱及生存的相关性
Biosci Rep. 2019 Jun 20;39(6). doi: 10.1042/BSR20182361. Print 2019 Jun 28.
7
Glioblastoma genetic drivers dictate the function of tumor-associated macrophages/microglia and responses to CSF1R inhibition.胶质母细胞瘤的遗传驱动因素决定了肿瘤相关巨噬细胞/小胶质细胞的功能以及对 CSF1R 抑制的反应。
Neuro Oncol. 2022 Apr 1;24(4):584-597. doi: 10.1093/neuonc/noab228.
8
Interactions between tumor-associated macrophages and tumor cells in glioblastoma: unraveling promising targeted therapies.脑胶质瘤中肿瘤相关巨噬细胞与肿瘤细胞的相互作用:探索有前景的靶向治疗方法。
Expert Rev Neurother. 2018 Sep;18(9):729-737. doi: 10.1080/14737175.2018.1510321. Epub 2018 Aug 22.
9
Glioblastoma-instructed microglia transition to heterogeneous phenotypic states with phagocytic and dendritic cell-like features in patient tumors and patient-derived orthotopic xenografts.胶质母细胞瘤诱导的小胶质细胞在患者肿瘤和患者来源的原位异种移植物中向具有吞噬细胞和树突状细胞样特征的异质表型状态转变。
Genome Med. 2024 Apr 2;16(1):51. doi: 10.1186/s13073-024-01321-8.
10
Microglia promote glioblastoma via mTOR-mediated immunosuppression of the tumour microenvironment.小胶质细胞通过 mTOR 介导的肿瘤微环境免疫抑制促进胶质母细胞瘤。
EMBO J. 2020 Aug 3;39(15):e103790. doi: 10.15252/embj.2019103790. Epub 2020 Jun 22.

引用本文的文献

1
Immune factors and their role in tumor aggressiveness in glioblastoma: Atypical cadherin FAT1 as a promising target for combating immune evasion.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.
2
The subventricular zone structure, function and implications for neurological disease.脑室下区的结构、功能及其对神经系统疾病的影响。
Genes Dis. 2024 Aug 26;12(3):101398. doi: 10.1016/j.gendis.2024.101398. eCollection 2025 May.
3
Microglia in pediatric brain tumors: The missing link to successful immunotherapy.

本文引用的文献

1
CCL3 Signaling in the Tumor Microenvironment.CCL3 在肿瘤微环境中的信号传导。
Adv Exp Med Biol. 2020;1231:13-21. doi: 10.1007/978-3-030-36667-4_2.
2
Microglia/Brain Macrophages as Central Drivers of Brain Tumor Pathobiology.小胶质细胞/脑巨噬细胞作为脑肿瘤病理生物学的核心驱动因素。
Neuron. 2019 Nov 6;104(3):442-449. doi: 10.1016/j.neuron.2019.08.028.
3
Transcriptomic Profiling of Adipose Derived Stem Cells Undergoing Osteogenesis by RNA-Seq.基于 RNA-Seq 的脂肪干细胞成骨过程中的转录组分析。
小儿脑肿瘤中的小胶质细胞:免疫治疗成功的缺失环节。
Cell Rep Med. 2023 Nov 21;4(11):101246. doi: 10.1016/j.xcrm.2023.101246. Epub 2023 Nov 3.
4
Integrative analysis of single-cell transcriptomics reveals age-associated immune landscape of glioblastoma.单细胞转录组学的综合分析揭示胶质母细胞瘤与年龄相关的免疫景观。
Front Immunol. 2023 Jan 24;14:1028775. doi: 10.3389/fimmu.2023.1028775. eCollection 2023.
5
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.
Sci Rep. 2019 Aug 13;9(1):11800. doi: 10.1038/s41598-019-48089-1.
4
Comprehensive Integration of Single-Cell Data.单细胞数据的综合整合。
Cell. 2019 Jun 13;177(7):1888-1902.e21. doi: 10.1016/j.cell.2019.05.031. Epub 2019 Jun 6.
5
Genetic and genomic alterations differentially dictate low-grade glioma growth through cancer stem cell-specific chemokine recruitment of T cells and microglia.遗传和基因组改变通过肿瘤干细胞特异性趋化因子募集 T 细胞和小胶质细胞,从而差异化地影响低级别神经胶质瘤的生长。
Neuro Oncol. 2019 Oct 9;21(10):1250-1262. doi: 10.1093/neuonc/noz080.
6
Cellular Senescence: Aging, Cancer, and Injury.细胞衰老:衰老、癌症和损伤。
Physiol Rev. 2019 Apr 1;99(2):1047-1078. doi: 10.1152/physrev.00020.2018.
7
Reference-based analysis of lung single-cell sequencing reveals a transitional profibrotic macrophage.基于参考的肺单细胞测序分析揭示了一种过渡性成纤维细胞样巨噬细胞。
Nat Immunol. 2019 Feb;20(2):163-172. doi: 10.1038/s41590-018-0276-y. Epub 2019 Jan 14.
8
The 2016 World Health Organization classification of tumours of the central nervous system.2016年世界卫生组织中枢神经系统肿瘤分类
Presse Med. 2018 Nov-Dec;47(11-12 Pt 2):e187-e200. doi: 10.1016/j.lpm.2018.04.015. Epub 2018 Nov 16.
9
TLR2 Promotes Glioma Immune Evasion by Downregulating MHC Class II Molecules in Microglia.TLR2 通过下调小胶质细胞 MHC Ⅱ类分子促进胶质瘤免疫逃逸。
Cancer Immunol Res. 2018 Oct;6(10):1220-1233. doi: 10.1158/2326-6066.CIR-18-0020. Epub 2018 Aug 21.
10
Phytosomal curcumin causes natural killer cell-dependent repolarization of glioblastoma (GBM) tumor-associated microglia/macrophages and elimination of GBM and GBM stem cells.姜黄素质体使神经细胞自然杀手依赖引起胶质母细胞瘤(GBM)肿瘤相关小胶质细胞/巨噬细胞的再极化并消除胶质母细胞瘤和胶质母细胞瘤干细胞。
J Exp Clin Cancer Res. 2018 Jul 25;37(1):168. doi: 10.1186/s13046-018-0792-5.