• 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

靶向神经胶质瘤干细胞的治疗策略。

Therapeutic strategies targeting glioblastoma stem cells.

机构信息

Neurooncology group, Biodonostia Institute, Paseo Dr. Beguiristain s/n, E-20014 San Sebastian, Spain.

出版信息

Recent Pat Anticancer Drug Discov. 2013 Sep;8(3):216-27. doi: 10.2174/15748928113089990002.

DOI:10.2174/15748928113089990002
PMID:23607282
Abstract

Glioblastoma is the most common, aggressive and lethal brain tumor in adults. However, current therapeutic protocols have low success rates and average overall survival is less than 15 months. The resistance to therapy is largely a result of the remarkable cellular and phenotypical heterogeneity that characterizes this type of tumor. The discovery of a subpopulation of cells exhibiting stem cell properties within the tumor bulk has profound implications for therapy as increasing evidence indicates that these cells, glioblastoma stem cells (GSCs), are responsible for the origin, maintenance and recurrence of the glioblastomas. These findings highlight the need to characterize GSCs in order to find novel treatments directly targeted specifically against them. In this review, we summarize the current knowledge regarding this issue, including some recent and relevant patents.

摘要

胶质母细胞瘤是成人中最常见、侵袭性最强和致命性的脑肿瘤。然而,目前的治疗方案成功率较低,平均总生存期不到 15 个月。治疗耐药性在很大程度上是由于这种肿瘤具有显著的细胞和表型异质性。在肿瘤块中发现具有干细胞特性的细胞亚群,这对治疗具有深远的意义,因为越来越多的证据表明,这些细胞,即胶质母细胞瘤干细胞(GSCs),是胶质母细胞瘤起源、维持和复发的原因。这些发现强调了需要对 GSCs 进行特征描述,以便找到针对它们的新型治疗方法。在这篇综述中,我们总结了关于这个问题的最新知识,包括一些最近的相关专利。

相似文献

1
Therapeutic strategies targeting glioblastoma stem cells.靶向神经胶质瘤干细胞的治疗策略。
Recent Pat Anticancer Drug Discov. 2013 Sep;8(3):216-27. doi: 10.2174/15748928113089990002.
2
Combined expressional analysis, bioinformatics and targeted proteomics identify new potential therapeutic targets in glioblastoma stem cells.联合表达分析、生物信息学和靶向蛋白质组学鉴定胶质母细胞瘤干细胞中的新潜在治疗靶点。
Oncotarget. 2015 Sep 22;6(28):26192-215. doi: 10.18632/oncotarget.4613.
3
The Importance of Tumor Stem Cells in Glioblastoma Resistance to Therapy.肿瘤干细胞在胶质母细胞瘤治疗耐药中的重要性
Int J Mol Sci. 2021 Apr 8;22(8):3863. doi: 10.3390/ijms22083863.
4
Targeting role of glioma stem cells for glioblastoma multiforme.针对多形性胶质母细胞瘤的神经胶质瘤干细胞靶向治疗。
Curr Med Chem. 2013;20(15):1974-84. doi: 10.2174/0929867311320150004.
5
Cancer Stem Cells: Significance in Origin, Pathogenesis and Treatment of Glioblastoma.癌症干细胞:在胶质母细胞瘤的起源、发病机制和治疗中的意义。
Cells. 2021 Mar 11;10(3):621. doi: 10.3390/cells10030621.
6
STAT3 as a Therapeutic Target for Glioblastoma.STAT3 作为胶质母细胞瘤的治疗靶点。
Anticancer Agents Med Chem. 2010 Sep;10(7):512-9. doi: 10.2174/187152010793498636.
7
Arsenic trioxide disrupts glioma stem cells via promoting PML degradation to inhibit tumor growth.三氧化二砷通过促进早幼粒细胞白血病蛋白(PML)降解来破坏胶质瘤干细胞,从而抑制肿瘤生长。
Oncotarget. 2015 Nov 10;6(35):37300-15. doi: 10.18632/oncotarget.5836.
8
The pro-tumorigenic effects of metabolic alterations in glioblastoma including brain tumor initiating cells.脑胶质瘤中代谢改变(包括脑肿瘤起始细胞)的促肿瘤作用。
Biochim Biophys Acta Rev Cancer. 2018 Apr;1869(2):175-188. doi: 10.1016/j.bbcan.2018.01.004. Epub 2018 Jan 31.
9
The role of octamer binding transcription factors in glioblastoma multiforme.八聚体结合转录因子在多形性胶质母细胞瘤中的作用。
Biochim Biophys Acta. 2016 Jun;1859(6):805-11. doi: 10.1016/j.bbagrm.2016.03.003. Epub 2016 Mar 8.
10
Ion channel expression patterns in glioblastoma stem cells with functional and therapeutic implications for malignancy.胶质母细胞瘤干细胞中的离子通道表达模式及其对恶性肿瘤的功能和治疗意义。
PLoS One. 2017 Mar 6;12(3):e0172884. doi: 10.1371/journal.pone.0172884. eCollection 2017.

引用本文的文献

1
Transcription Factor CEBPD-Mediated WTAP Facilitates the Stemness, Growth, Migration and Glycolysis of Glioblastoma Stem Like Cells.转录因子CEBPD介导的WTAP促进胶质母细胞瘤干细胞样细胞的干性、生长、迁移和糖酵解
Neurochem Res. 2025 Feb 13;50(2):100. doi: 10.1007/s11064-024-04321-7.
2
TENT5A Increases Glioma Malignancy and Promotes its Progression.TENT5A增加胶质瘤恶性程度并促进其进展。
Recent Pat Anticancer Drug Discov. 2025;20(1):45-54. doi: 10.2174/0115748928280901231206102637.
3
Deletion of () Decreases SOX2 Malignant Activity in Glioblastoma.
()的缺失降低了胶质母细胞瘤中SOX2的恶性活性。
Cancers (Basel). 2021 Mar 29;13(7):1574. doi: 10.3390/cancers13071574.
4
Liquid Biopsy in Glioblastoma: Opportunities, Applications and Challenges.胶质母细胞瘤中的液体活检:机遇、应用与挑战
Cancers (Basel). 2019 Jul 5;11(7):950. doi: 10.3390/cancers11070950.
5
PR-LncRNA signature regulates glioma cell activity through expression of SOX factors.PR-LncRNA 特征通过 SOX 因子表达调控神经胶质瘤细胞活性。
Sci Rep. 2018 Aug 24;8(1):12746. doi: 10.1038/s41598-018-30836-5.
6
Integrin α7: a novel promising target in glioblastoma stem cells.整合素α7:胶质母细胞瘤干细胞中一个新的有前景的靶点。
Stem Cell Investig. 2018 Jan 13;5:2. doi: 10.21037/sci.2017.12.05. eCollection 2018.
7
High expression of MKP1/DUSP1 counteracts glioma stem cell activity and mediates HDAC inhibitor response.MKP1/DUSP1的高表达可抵消胶质瘤干细胞活性并介导HDAC抑制剂反应。
Oncogenesis. 2017 Dec 14;6(12):401. doi: 10.1038/s41389-017-0003-9.
8
Targeting SOX2 as a Therapeutic Strategy in Glioblastoma.靶向SOX2作为胶质母细胞瘤的一种治疗策略
Front Oncol. 2016 Oct 24;6:222. doi: 10.3389/fonc.2016.00222. eCollection 2016.
9
Paradoxical role of SOX2 in gastric cancer.SOX2在胃癌中的矛盾作用。
Am J Cancer Res. 2016 Mar 15;6(4):701-13. eCollection 2016.
10
mTOR inhibition decreases SOX2-SOX9 mediated glioma stem cell activity and temozolomide resistance.mTOR抑制可降低SOX2 - SOX9介导的胶质瘤干细胞活性及替莫唑胺耐药性。
Expert Opin Ther Targets. 2016;20(4):393-405. doi: 10.1517/14728222.2016.1151002.