• 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

胶质母细胞瘤中的凋亡信号通路及其治疗意义。

Apoptotic Signaling Pathways in Glioblastoma and Therapeutic Implications.

机构信息

Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, Mexico.

Departamento de Farmacología, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de México, Mexico.

出版信息

Biomed Res Int. 2017;2017:7403747. doi: 10.1155/2017/7403747. Epub 2017 Nov 12.

DOI:10.1155/2017/7403747
PMID:29259986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5702396/
Abstract

Glioblastoma multiforme (GBM) is the most hostile type of brain cancer. Its aggressiveness is due to increased invasion, migration, proliferation, angiogenesis, and a decreased apoptosis. In this review, we discuss the role of key regulators of apoptosis in GBM and glioblastoma stem cells. Given their importance in the etiology and pathogenesis of GBM, these signaling molecules may represent potential therapeutic targets.

摘要

多形性胶质母细胞瘤(GBM)是最具侵袭性的脑癌。其侵袭性归因于细胞的过度侵袭、迁移、增殖、血管生成,以及细胞凋亡减少。在这篇综述中,我们讨论了凋亡关键调节因子在 GBM 和胶质母细胞瘤干细胞中的作用。鉴于它们在 GBM 的病因和发病机制中的重要性,这些信号分子可能代表潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b905/5702396/50128b5de583/BMRI2017-7403747.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b905/5702396/156145e0584b/BMRI2017-7403747.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b905/5702396/50128b5de583/BMRI2017-7403747.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b905/5702396/156145e0584b/BMRI2017-7403747.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b905/5702396/50128b5de583/BMRI2017-7403747.002.jpg

相似文献

1
Apoptotic Signaling Pathways in Glioblastoma and Therapeutic Implications.胶质母细胞瘤中的凋亡信号通路及其治疗意义。
Biomed Res Int. 2017;2017:7403747. doi: 10.1155/2017/7403747. Epub 2017 Nov 12.
2
Silencing of PROS1 induces apoptosis and inhibits migration and invasion of glioblastoma multiforme cells.PROS1基因沉默可诱导多形性胶质母细胞瘤细胞凋亡,并抑制其迁移和侵袭。
Int J Oncol. 2016 Dec;49(6):2359-2366. doi: 10.3892/ijo.2016.3755. Epub 2016 Nov 3.
3
IL-8/CXCR1/2 signalling promotes tumor cell proliferation, invasion and vascular mimicry in glioblastoma.白细胞介素-8/CXCR1/2 信号通路促进脑胶质母细胞瘤中肿瘤细胞的增殖、侵袭和血管拟态形成。
J Biomed Sci. 2018 Aug 8;25(1):62. doi: 10.1186/s12929-018-0464-y.
4
Tumor suppressor miR-181c attenuates proliferation, invasion, and self-renewal abilities in glioblastoma.肿瘤抑制因子miR-181c减弱胶质母细胞瘤的增殖、侵袭和自我更新能力。
Neuroreport. 2015 Jan 21;26(2):66-73. doi: 10.1097/WNR.0000000000000302.
5
Up-regulated circular RNA hsa_circ_0067934 contributes to glioblastoma progression through activating PI3K-AKT pathway.上调的环状 RNA hsa_circ_0067934 通过激活 PI3K-AKT 通路促进胶质母细胞瘤进展。
Eur Rev Med Pharmacol Sci. 2019 Apr;23(8):3447-3454. doi: 10.26355/eurrev_201904_17709.
6
EGFRvIII-Stat5 Signaling Enhances Glioblastoma Cell Migration and Survival.EGFRvIII-Stat5 信号增强胶质母细胞瘤细胞迁移和存活。
Mol Cancer Res. 2018 Jul;16(7):1185-1195. doi: 10.1158/1541-7786.MCR-18-0125. Epub 2018 May 3.
7
TRIP13 promotes the cell proliferation, migration and invasion of glioblastoma through the FBXW7/c-MYC axis.TRIP13 通过 FBXW7/c-MYC 轴促进脑胶质瘤的细胞增殖、迁移和侵袭。
Br J Cancer. 2019 Dec;121(12):1069-1078. doi: 10.1038/s41416-019-0633-0. Epub 2019 Nov 19.
8
Potential mechanisms of microRNA-129-5p in inhibiting cell processes including viability, proliferation, migration and invasiveness of glioblastoma cells U87 through targeting FNDC3B.微小RNA-129-5p通过靶向含III型纤连蛋白结构域蛋白3B抑制胶质母细胞瘤细胞U87的细胞活性、增殖、迁移和侵袭等过程的潜在机制。
Biomed Pharmacother. 2017 Mar;87:405-411. doi: 10.1016/j.biopha.2016.12.100. Epub 2017 Jan 6.
9
HOXB13 promotes proliferation, migration, and invasion of glioblastoma through transcriptional upregulation of lncRNA HOXC-AS3.HOXB13 通过转录上调长链非编码 RNA HOXC-AS3 促进脑胶质瘤的增殖、迁移和侵袭。
J Cell Biochem. 2019 Sep;120(9):15527-15537. doi: 10.1002/jcb.28819. Epub 2019 May 6.
10
miRNA-429 Inhibits Astrocytoma Proliferation and Invasion by Targeting BMI1.微小RNA-429通过靶向BMI1抑制星形细胞瘤的增殖和侵袭。
Pathol Oncol Res. 2017 Apr;23(2):369-376. doi: 10.1007/s12253-016-0113-2. Epub 2016 Sep 23.

引用本文的文献

1
Ferroptosis as a therapeutic target in glioblastoma: Mechanisms and emerging strategies.铁死亡作为胶质母细胞瘤的治疗靶点:机制与新兴策略
Mol Ther Nucleic Acids. 2025 Jul 30;36(3):102649. doi: 10.1016/j.omtn.2025.102649. eCollection 2025 Sep 9.
2
SCD1 and SCD5 Modulate PARP-Dependent DNA Repair via Fatty Acid Desaturation in Glioblastoma.在胶质母细胞瘤中,硬脂酰辅酶A去饱和酶1(SCD1)和硬脂酰辅酶A去饱和酶5(SCD5)通过脂肪酸去饱和作用调节聚(ADP-核糖)聚合酶(PARP)依赖性DNA修复。
bioRxiv. 2025 Jul 27:2025.07.23.666454. doi: 10.1101/2025.07.23.666454.
3
Quantitative Proteomic Analysis Reveals Different Functional Subtypes among -Wildtype Glioblastoma.

本文引用的文献

1
Contribution of the Microenvironmental Niche to Glioblastoma Heterogeneity.微环境龛对胶质母细胞瘤异质性的贡献。
Biomed Res Int. 2017;2017:9634172. doi: 10.1155/2017/9634172. Epub 2017 May 28.
2
Correction of PTEN mutations in glioblastoma cell lines via AAV-mediated gene editing.通过腺相关病毒(AAV)介导的基因编辑纠正胶质母细胞瘤细胞系中的PTEN突变。
PLoS One. 2017 May 2;12(5):e0176683. doi: 10.1371/journal.pone.0176683. eCollection 2017.
3
Expression of CD133 and CD44 in glioblastoma stem cells correlates with cell proliferation, phenotype stability and intra-tumor heterogeneity.
定量蛋白质组学分析揭示野生型胶质母细胞瘤中的不同功能亚型。
J Proteome Res. 2025 Jul 4;24(7):3610-3624. doi: 10.1021/acs.jproteome.5c00199. Epub 2025 Jun 15.
4
Doxorubicin and NFL-TBS.40-63 peptide loaded gold nanoparticles as a multimodal therapy of glioblastoma.阿霉素和负载NFL-TBS.40-63肽的金纳米颗粒作为胶质母细胞瘤的多模态治疗方法。
Discov Nano. 2025 Apr 28;20(1):72. doi: 10.1186/s11671-025-04249-z.
5
Chitinase-3-like-1: a multifaceted player in neuroinflammation and degenerative pathologies with therapeutic implications.几丁质酶-3样蛋白1:神经炎症和退行性病变中具有多方面作用且具有治疗意义的因子。
Mol Neurodegener. 2025 Jan 18;20(1):7. doi: 10.1186/s13024-025-00801-8.
6
Beta-Caryophyllene Augments Radiotherapy Efficacy in GBM by Modulating Cell Apoptosis and DNA Damage Repair via PPARγ and NF-κB Pathways.β-石竹烯通过PPARγ和NF-κB途径调节细胞凋亡和DNA损伤修复增强胶质母细胞瘤的放疗疗效。
Phytother Res. 2025 Feb;39(2):776-788. doi: 10.1002/ptr.8413. Epub 2024 Dec 13.
7
Curcumin as a novel therapeutic candidate for cancer: can this natural compound revolutionize cancer treatment?姜黄素作为一种新型癌症治疗候选药物:这种天然化合物能否彻底改变癌症治疗方式?
Front Oncol. 2024 Oct 23;14:1438040. doi: 10.3389/fonc.2024.1438040. eCollection 2024.
8
Cell death in glioblastoma and the central nervous system.胶质母细胞瘤和中枢神经系统中的细胞死亡
Cell Oncol (Dordr). 2025 Apr;48(2):313-349. doi: 10.1007/s13402-024-01007-8. Epub 2024 Nov 6.
9
Synergism of d-limonene and temozolomide on migratory and apoptotic behaviors of human glioblastoma cell lines.d-柠檬烯与替莫唑胺对人胶质母细胞瘤细胞系迁移和凋亡行为的协同作用。
Bioimpacts. 2024;14(5):27681. doi: 10.34172/bi.2023.27681. Epub 2023 Oct 24.
10
Combining the constitutive TRAIL-secreting induced neural stem cell therapy with the novel anti-cancer drug TR-107 in glioblastoma.将组成型分泌肿瘤坏死因子相关凋亡诱导配体的诱导神经干细胞疗法与新型抗癌药物TR-107联合用于胶质母细胞瘤治疗。
Mol Ther Oncol. 2024 Jun 15;32(3):200834. doi: 10.1016/j.omton.2024.200834. eCollection 2024 Sep 19.
胶质母细胞瘤干细胞中CD133和CD44的表达与细胞增殖、表型稳定性及肿瘤内异质性相关。
PLoS One. 2017 Feb 27;12(2):e0172791. doi: 10.1371/journal.pone.0172791. eCollection 2017.
4
Overexpression of miR-29a reduces the oncogenic properties of glioblastoma stem cells by downregulating Quaking gene isoform 6.miR-29a的过表达通过下调震颤基因亚型6降低胶质母细胞瘤干细胞的致癌特性。
Oncotarget. 2017 Apr 11;8(15):24949-24963. doi: 10.18632/oncotarget.15327.
5
CRISPR-Cas9: from Genome Editing to Cancer Research.CRISPR-Cas9:从基因组编辑到癌症研究
Int J Biol Sci. 2016 Nov 4;12(12):1427-1436. doi: 10.7150/ijbs.17421. eCollection 2016.
6
Cancer stem cells: understanding tumor hierarchy and heterogeneity.癌症干细胞:理解肿瘤层级结构与异质性
Medicine (Baltimore). 2016 Sep;95(1 Suppl 1):S2-S7. doi: 10.1097/MD.0000000000004764.
7
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.
8
Effects of PI3K inhibitor NVP-BKM120 on overcoming drug resistance and eliminating cancer stem cells in human breast cancer cells.PI3K抑制剂NVP-BKM120对克服人乳腺癌细胞耐药性及消除癌干细胞的作用
Cell Death Dis. 2015 Dec 17;6(12):e2020. doi: 10.1038/cddis.2015.363.
9
Role of mTOR in glioblastoma.雷帕霉素靶蛋白(mTOR)在胶质母细胞瘤中的作用。
Gene. 2016 Jan 10;575(2 Pt 1):187-90. doi: 10.1016/j.gene.2015.08.060. Epub 2015 Sep 1.
10
Cardamonin induces apoptosis by suppressing STAT3 signaling pathway in glioblastoma stem cells.小豆蔻明通过抑制胶质母细胞瘤干细胞中的STAT3信号通路诱导细胞凋亡。
Tumour Biol. 2015 Dec;36(12):9667-76. doi: 10.1007/s13277-015-3673-y. Epub 2015 Jul 7.