• 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

作为免疫治疗靶点的胶质瘤干细胞:进展与挑战

Glioma Stem Cells as Immunotherapeutic Targets: Advancements and Challenges.

作者信息

Piper Keenan, DePledge Lisa, Karsy Michael, Cobbs Charles

机构信息

Ben & Catherine Ivy Center for Advanced Brain Tumor Treatment, Swedish Neuroscience Institute, Seattle, WA, United States.

Sidney Kimmel Medical College, Philadelphia, PA, United States.

出版信息

Front Oncol. 2021 Feb 24;11:615704. doi: 10.3389/fonc.2021.615704. eCollection 2021.

DOI:10.3389/fonc.2021.615704
PMID:33718170
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7945033/
Abstract

Glioblastoma is the most common and lethal primary brain malignancy. Despite major investments in research into glioblastoma biology and drug development, treatment remains limited and survival has not substantially improved beyond 1-2 years. Cancer stem cells (CSC) or glioma stem cells (GSC) refer to a population of tumor originating cells capable of self-renewal and differentiation. While controversial and challenging to study, evidence suggests that GCSs may result in glioblastoma tumor recurrence and resistance to treatment. Multiple treatment strategies have been suggested at targeting GCSs, including immunotherapy, posttranscriptional regulation, modulation of the tumor microenvironment, and epigenetic modulation. In this review, we discuss recent advances in glioblastoma treatment specifically focused on targeting of GCSs as well as their potential integration into current clinical pathways and trials.

摘要

胶质母细胞瘤是最常见且致命的原发性脑恶性肿瘤。尽管在胶质母细胞瘤生物学研究和药物开发方面投入巨大,但治疗手段仍然有限,患者生存期在1至2年之后并无显著改善。癌症干细胞(CSC)或胶质瘤干细胞(GSC)是指一群具有自我更新和分化能力的肿瘤起源细胞。虽然对其研究存在争议且颇具挑战,但有证据表明,胶质瘤干细胞可能导致胶质母细胞瘤肿瘤复发和治疗耐药。针对胶质瘤干细胞已提出多种治疗策略,包括免疫疗法、转录后调控、肿瘤微环境调节以及表观遗传调节。在本综述中,我们将讨论胶质母细胞瘤治疗的最新进展,特别关注针对胶质瘤干细胞的治疗方法,以及它们融入当前临床路径和试验的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7076/7945033/2aa6c261823c/fonc-11-615704-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7076/7945033/33c176e433a4/fonc-11-615704-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7076/7945033/7774a97d0a4a/fonc-11-615704-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7076/7945033/2aa6c261823c/fonc-11-615704-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7076/7945033/33c176e433a4/fonc-11-615704-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7076/7945033/7774a97d0a4a/fonc-11-615704-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7076/7945033/2aa6c261823c/fonc-11-615704-g003.jpg

相似文献

1
Glioma Stem Cells as Immunotherapeutic Targets: Advancements and Challenges.作为免疫治疗靶点的胶质瘤干细胞:进展与挑战
Front Oncol. 2021 Feb 24;11:615704. doi: 10.3389/fonc.2021.615704. eCollection 2021.
2
Glioma Stem Cells: Signaling, Microenvironment, and Therapy.胶质瘤干细胞:信号传导、微环境与治疗
Stem Cells Int. 2016;2016:7849890. doi: 10.1155/2016/7849890. Epub 2016 Jan 6.
3
Immunotherapy targeting glioma stem cells--insights and perspectives.针对神经胶质瘤干细胞的免疫疗法——见解与展望。
Expert Opin Biol Ther. 2012 Feb;12(2):165-78. doi: 10.1517/14712598.2012.648180. Epub 2011 Dec 26.
4
Impairing temozolomide resistance driven by glioma stem-like cells with adjuvant immunotherapy targeting O-acetyl GD2 ganglioside.用针对 O-乙酰基 GD2 神经节苷脂的辅助免疫疗法来削弱由神经胶质瘤干细胞驱动的替莫唑胺耐药性。
Int J Cancer. 2020 Jan 15;146(2):424-438. doi: 10.1002/ijc.32533. Epub 2019 Jul 13.
5
Chromatin remodeler HELLS maintains glioma stem cells through E2F3 and MYC.染色质重塑酶 HELLS 通过 E2F3 和 MYC 维持神经胶质瘤干细胞。
JCI Insight. 2019 Apr 4;4(7). doi: 10.1172/jci.insight.126140.
6
Potential Therapeutic Effects of the Neural Stem Cell-Targeting Antibody Nilo1 in Patient-Derived Glioblastoma Stem Cells.靶向神经干细胞的抗体Nilo1对患者来源的胶质母细胞瘤干细胞的潜在治疗作用
Front Oncol. 2020 Aug 14;10:1665. doi: 10.3389/fonc.2020.01665. eCollection 2020.
7
Mechanisms regulating radiosensitivity of glioma stem cells.调控脑胶质瘤干细胞放射敏感性的机制。
Neoplasma. 2017;64(5):655-665. doi: 10.4149/neo_2017_502.
8
Glioblastoma Therapy: Past, Present and Future.胶质母细胞瘤治疗:过去、现在和未来。
Int J Mol Sci. 2024 Feb 21;25(5):2529. doi: 10.3390/ijms25052529.
9
The interference of Notch1 target Hes1 affects cell growth, differentiation and invasiveness of glioblastoma stem cells through modulation of multiple oncogenic targets.Notch1靶点Hes1的干扰通过调节多个致癌靶点影响胶质母细胞瘤干细胞的细胞生长、分化和侵袭性。
Oncotarget. 2017 Mar 14;8(11):17873-17886. doi: 10.18632/oncotarget.15013.
10
shRNA-mediated PPARα knockdown in human glioma stem cells reduces in vitro proliferation and inhibits orthotopic xenograft tumour growth.shRNA 介导的人胶质瘤干细胞中 PPARα 的敲低可降低体外增殖并抑制原位异种移植肿瘤生长。
J Pathol. 2019 Apr;247(4):422-434. doi: 10.1002/path.5201. Epub 2018 Dec 27.

引用本文的文献

1
Stem cell therapies and glioma stem cells in glioblastoma: a systematic review of current challenges and research directions.胶质母细胞瘤中的干细胞疗法与胶质瘤干细胞:当前挑战及研究方向的系统综述
Int J Emerg Med. 2025 Aug 6;18(1):144. doi: 10.1186/s12245-025-00921-4.
2
In Vitro Functional Validation of an Anti-FREM2 Nanobody for Glioblastoma Cell Targeting.用于靶向胶质母细胞瘤细胞的抗FREM2纳米抗体的体外功能验证
Antibodies (Basel). 2025 Jan 24;14(1):8. doi: 10.3390/antib14010008.
3
Cell-Based Glioma Models for Anticancer Drug Screening: From Conventional Adherent Cell Cultures to Tumor-Specific Three-Dimensional Constructs.

本文引用的文献

1
Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy.单细胞 RNA 测序揭示胶质母细胞瘤再现了正常的神经发育层次结构。
Nat Commun. 2020 Jul 8;11(1):3406. doi: 10.1038/s41467-020-17186-5.
2
Glioblastoma-mediated Immune Dysfunction Limits CMV-specific T Cells and Therapeutic Responses: Results from a Phase I/II Trial.胶质母细胞瘤介导的免疫功能障碍限制了 CMV 特异性 T 细胞和治疗反应:来自 I/II 期试验的结果。
Clin Cancer Res. 2020 Jul 15;26(14):3565-3577. doi: 10.1158/1078-0432.CCR-20-0176. Epub 2020 Apr 16.
3
Chlorotoxin-directed CAR T cells for specific and effective targeting of glioblastoma.
用于抗癌药物筛选的基于细胞的胶质瘤模型:从传统贴壁细胞培养到肿瘤特异性三维构建体
Cells. 2024 Dec 17;13(24):2085. doi: 10.3390/cells13242085.
4
Exploring miRNA therapies and gut microbiome-enhanced CAR-T cells: advancing frontiers in glioblastoma stem cell targeting.探索微小RNA疗法和肠道微生物群增强的嵌合抗原受体T细胞:推进胶质母细胞瘤干细胞靶向治疗的前沿进展。
Naunyn Schmiedebergs Arch Pharmacol. 2025 Mar;398(3):2169-2207. doi: 10.1007/s00210-024-03479-9. Epub 2024 Oct 9.
5
Insights of immune cell heterogeneity, tumor-initiated subtype transformation, drug resistance, treatment and detecting technologies in glioma microenvironment.胶质瘤微环境中免疫细胞异质性、肿瘤起始亚型转化、耐药性、治疗及检测技术的见解
J Adv Res. 2025 Jun;72:527-554. doi: 10.1016/j.jare.2024.07.033. Epub 2024 Aug 5.
6
The Epigenetic Modifiers HDAC2 and HDAC7 Inversely Associate with Cancer Stemness and Immunity in Solid Tumors.组蛋白去乙酰化酶 2 和 7 作为表观遗传修饰物在实体瘤中与癌症干性和免疫呈负相关。
Int J Mol Sci. 2024 Jul 17;25(14):7841. doi: 10.3390/ijms25147841.
7
The potential of miRNA-based approaches in glioblastoma: An update in current advances and future perspectives.基于微小RNA的方法在胶质母细胞瘤中的潜力:当前进展与未来展望的最新情况
Curr Res Pharmacol Drug Discov. 2024 Jun 29;7:100193. doi: 10.1016/j.crphar.2024.100193. eCollection 2024.
8
The tumour microenvironment, treatment resistance and recurrence in glioblastoma.脑胶质瘤中的肿瘤微环境、治疗抵抗和复发。
J Transl Med. 2024 Jun 6;22(1):540. doi: 10.1186/s12967-024-05301-9.
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
Glioma Stem Cells-Features for New Therapy Design.胶质瘤干细胞——新型治疗设计的特征
Cancers (Basel). 2024 Apr 19;16(8):1557. doi: 10.3390/cancers16081557.
用于特异性有效靶向胶质母细胞瘤的氯毒素导向嵌合抗原受体T细胞。
Sci Transl Med. 2020 Mar 4;12(533). doi: 10.1126/scitranslmed.aaw2672.
4
Rindopepimut with Bevacizumab for Patients with Relapsed EGFRvIII-Expressing Glioblastoma (ReACT): Results of a Double-Blind Randomized Phase II Trial.Rindopepimut 联合贝伐珠单抗治疗复发性 EGFRvIII 表达型胶质母细胞瘤(ReACT):一项双盲随机 II 期试验的结果。
Clin Cancer Res. 2020 Apr 1;26(7):1586-1594. doi: 10.1158/1078-0432.CCR-18-1140. Epub 2020 Feb 7.
5
The Extracellular Matrix and Biocompatible Materials in Glioblastoma Treatment.胶质母细胞瘤治疗中的细胞外基质与生物相容性材料
Front Bioeng Biotechnol. 2019 Nov 19;7:341. doi: 10.3389/fbioe.2019.00341. eCollection 2019.
6
CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2012-2016.美国 2012-2016 年诊断的原发性脑和其他中枢神经系统肿瘤 CBTRUS 统计报告。
Neuro Oncol. 2019 Nov 1;21(Suppl 5):v1-v100. doi: 10.1093/neuonc/noz150.
7
The dystroglycan receptor maintains glioma stem cells in the vascular niche.黏着蛋白聚糖受体维持血管龛中的神经胶质瘤干细胞。
Acta Neuropathol. 2019 Dec;138(6):1033-1052. doi: 10.1007/s00401-019-02069-x. Epub 2019 Aug 28.
8
Glioblastoma stem cells: lessons from the tumor hierarchy in a lethal cancer.胶质母细胞瘤干细胞:致命癌症中肿瘤等级的启示。
Genes Dev. 2019 Jun 1;33(11-12):591-609. doi: 10.1101/gad.324301.119.
9
Evolutionary Trajectories of IDH Glioblastomas Reveal a Common Path of Early Tumorigenesis Instigated Years ahead of Initial Diagnosis.IDH 胶质母细胞瘤的进化轨迹揭示了一种常见的早期肿瘤发生途径,其起始时间早于初始诊断数年。
Cancer Cell. 2019 Apr 15;35(4):692-704.e12. doi: 10.1016/j.ccell.2019.02.007. Epub 2019 Mar 21.
10
Pilot Trial of Adoptive Transfer of Chimeric Antigen Receptor-transduced T Cells Targeting EGFRvIII in Patients With Glioblastoma.嵌合抗原受体修饰的 T 细胞过继转移治疗胶质母细胞瘤患者中针对 EGFRvIII 的初步临床试验
J Immunother. 2019 May;42(4):126-135. doi: 10.1097/CJI.0000000000000260.