• 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

鉴定和功能表征参与胶质瘤恶性进展的 microRNAs。

Identification and functional characterization of microRNAs involved in the malignant progression of gliomas.

机构信息

Department of Neuropathology, Heinrich-Heine-University, Düsseldorf, Germany.

出版信息

Brain Pathol. 2010 May;20(3):539-50. doi: 10.1111/j.1750-3639.2009.00328.x. Epub 2009 Sep 19.

DOI:10.1111/j.1750-3639.2009.00328.x
PMID:19775293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8094849/
Abstract

Diffuse astrocytoma of World Health Organization (WHO) grade II has an inherent tendency to spontaneously progress to anaplastic astrocytoma WHO grade III or secondary glioblastoma WHO grade IV. We explored the role of microRNAs (miRNAs) in glioma progression by investigating the expression profiles of 157 miRNAs in four patients with primary WHO grade II gliomas that spontaneously progressed to WHO grade IV secondary glioblastomas. Thereby, we identified 12 miRNAs (miR-9, miR-15a, miR-16, miR-17, miR-19a, miR-20a, miR-21, miR-25, miR-28, miR-130b, miR-140 and miR-210) showing increased expression, and two miRNAs (miR-184 and miR-328) showing reduced expression upon progression. Validation experiments on independent series of primary low-grade and secondary high-grade astrocytomas confirmed miR-17 and miR-184 as promising candidates, which were selected for functional analyses. These studies revealed miRNA-specific influences on the viability, proliferation, apoptosis and invasive growth properties of A172 and T98G glioma cells in vitro. Using mRNA and protein expression profiling, we identified distinct sets of transcripts and proteins that were differentially expressed after inhibition of miR-17 or overexpression of miR-184 in glioma cells. Taken together, our results support an important role of altered miRNA expression in gliomas, and suggest miR-17 and miR-184 as interesting candidates contributing to glioma progression.

摘要

弥漫性脑星形细胞瘤(世界卫生组织 [WHO] 分级 II)具有自发进展为间变性星形细胞瘤(WHO 分级 III)或继发性胶质母细胞瘤(WHO 分级 IV)的固有倾向。我们通过研究 4 名原发性 WHO 分级 II 脑胶质瘤患者的 miRNA 表达谱,探讨了 miRNA 在胶质瘤进展中的作用,这些患者的肿瘤自发进展为 WHO 分级 IV 继发性胶质母细胞瘤。因此,我们确定了 12 个 miRNA(miR-9、miR-15a、miR-16、miR-17、miR-19a、miR-20a、miR-21、miR-25、miR-28、miR-130b、miR-140 和 miR-210)表达上调,2 个 miRNA(miR-184 和 miR-328)表达下调。在独立的原发性低级别和继发性高级别星形细胞瘤系列中进行的验证实验证实了 miR-17 和 miR-184 是很有前途的候选物,随后对其进行了功能分析。这些研究揭示了 miRNA 对 A172 和 T98G 神经胶质瘤细胞体外活力、增殖、凋亡和侵袭生长特性的特异性影响。利用 mRNA 和蛋白质表达谱分析,我们确定了在抑制 miR-17 或过表达 miR-184 后,胶质瘤细胞中差异表达的不同转录本和蛋白质集。总之,我们的研究结果支持 miRNA 表达改变在胶质瘤中的重要作用,并表明 miR-17 和 miR-184 是促进胶质瘤进展的有趣候选物。

相似文献

1
Identification and functional characterization of microRNAs involved in the malignant progression of gliomas.鉴定和功能表征参与胶质瘤恶性进展的 microRNAs。
Brain Pathol. 2010 May;20(3):539-50. doi: 10.1111/j.1750-3639.2009.00328.x. Epub 2009 Sep 19.
2
MiRNA expression profiling in human gliomas: upregulated miR-363 increases cell survival and proliferation.人类胶质瘤中的微小RNA表达谱分析:上调的miR-363可提高细胞存活率和增殖能力。
Tumour Biol. 2016 Oct;37(10):14035-14048. doi: 10.1007/s13277-016-5273-x. Epub 2016 Aug 6.
3
MiR-16-5p is frequently down-regulated in astrocytic gliomas and modulates glioma cell proliferation, apoptosis and response to cytotoxic therapy.miR-16-5p 在星形细胞瘤中经常下调,并调节神经胶质瘤细胞的增殖、凋亡和对细胞毒治疗的反应。
Neuropathol Appl Neurobiol. 2019 Aug;45(5):441-458. doi: 10.1111/nan.12532. Epub 2019 Feb 19.
4
Up-regulation of microRNA-15b correlates with unfavorable prognosis and malignant progression of human glioma.微小RNA-15b的上调与人类胶质瘤的不良预后和恶性进展相关。
Int J Clin Exp Pathol. 2015 May 1;8(5):4943-52. eCollection 2015.
5
Characterization of gene expression profiles associated with glioma progression using oligonucleotide-based microarray analysis and real-time reverse transcription-polymerase chain reaction.使用基于寡核苷酸的微阵列分析和实时逆转录-聚合酶链反应对与胶质瘤进展相关的基因表达谱进行表征。
Am J Pathol. 2003 Sep;163(3):1033-43. doi: 10.1016/S0002-9440(10)63463-3.
6
High miR-196a and low miR-367 cooperatively correlate with unfavorable prognosis of high-grade glioma.高表达的miR-196a和低表达的miR-367与高级别胶质瘤的不良预后协同相关。
Int J Clin Exp Pathol. 2015 Jun 1;8(6):6576-88. eCollection 2015.
7
MicroRNA expression patterns in the malignant progression of gliomas and a 5-microRNA signature for prognosis.胶质瘤恶性进展中的微小RNA表达模式及一种用于预后评估的5-微小RNA特征
Oncotarget. 2014 Dec 30;5(24):12908-15. doi: 10.18632/oncotarget.2679.
8
Role of microRNAs Located on Chromosome Arm 10q in Malignant Gliomas.位于染色体10q臂上的微小RNA在恶性胶质瘤中的作用
Brain Pathol. 2016 May;26(3):344-58. doi: 10.1111/bpa.12294. Epub 2015 Sep 9.
9
MiR-328 promotes glioma cell invasion via SFRP1-dependent Wnt-signaling activation.miR-328 通过 SFRP1 依赖性 Wnt 信号激活促进神经胶质瘤细胞侵袭。
Neuro Oncol. 2014 Jan;16(2):179-90. doi: 10.1093/neuonc/not164. Epub 2013 Dec 4.
10
MiR-145 functions as a tumor-suppressive RNA by targeting Sox9 and adducin 3 in human glioma cells.miR-145 通过靶向 Sox9 和 adducin 3 在人神经胶质瘤细胞中发挥肿瘤抑制 RNA 的功能。
Neuro Oncol. 2013 Oct;15(10):1302-16. doi: 10.1093/neuonc/not090. Epub 2013 Jun 28.

引用本文的文献

1
miR-210 loss leads to widespread phenotypic and gene expression changes in human 293T cells.miR-210缺失导致人类293T细胞中广泛的表型和基因表达变化。
Front Genet. 2024 Dec 16;15:1486252. doi: 10.3389/fgene.2024.1486252. eCollection 2024.
2
Hypoxic glioma-derived exosomal miR-25-3p promotes macrophage M2 polarization by activating the PI3K-AKT-mTOR signaling pathway.低氧胶质瘤衍生的外泌体 miR-25-3p 通过激活 PI3K-AKT-mTOR 信号通路促进巨噬细胞 M2 极化。
J Nanobiotechnology. 2024 Oct 16;22(1):628. doi: 10.1186/s12951-024-02888-5.
3
Genomic, epigenomic and transcriptomic landscape of glioblastoma.胶质母细胞瘤的基因组、表观基因组和转录组景观。
Metab Brain Dis. 2024 Dec;39(8):1591-1611. doi: 10.1007/s11011-024-01414-8. Epub 2024 Aug 24.
4
Circulating Liquid Biopsy Biomarkers in Glioblastoma: Advances and Challenges.循环液体活检生物标志物在胶质母细胞瘤中的应用:进展与挑战。
Int J Mol Sci. 2024 Jul 21;25(14):7974. doi: 10.3390/ijms25147974.
5
Liquid Biopsy in Whole Blood for Identification of Gene Expression Patterns (mRNA and miRNA) Associated with Recurrence of Glioblastoma WHO CNS Grade 4.全血液体活检用于鉴定与胶质母细胞瘤WHO CNS 4级复发相关的基因表达模式(mRNA和miRNA)
Cancers (Basel). 2024 Jun 26;16(13):2345. doi: 10.3390/cancers16132345.
6
Polyphenols Modulate the miRNAs Expression that Involved in Glioblastoma.多酚调节涉及神经胶质瘤的 miRNAs 表达。
Mini Rev Med Chem. 2024;24(21):1953-1969. doi: 10.2174/0113895575304605240408105201.
7
Liquid biopsy for improving diagnosis and monitoring of CNS lymphomas: A RANO review.液体活检提高中枢神经系统淋巴瘤诊断和监测的价值:一项 RANO 综述。
Neuro Oncol. 2024 Jun 3;26(6):993-1011. doi: 10.1093/neuonc/noae032.
8
MicroRNA as a potential diagnostic and prognostic biomarker in brain gliomas: a systematic review and meta-analysis.微小RNA作为脑胶质瘤潜在的诊断和预后生物标志物:一项系统综述和荟萃分析
Front Neurol. 2024 Feb 29;15:1357321. doi: 10.3389/fneur.2024.1357321. eCollection 2024.
9
Use of microRNAs as Diagnostic, Prognostic, and Therapeutic Tools for Glioblastoma.微小RNA作为胶质母细胞瘤的诊断、预后和治疗工具的应用
Int J Mol Sci. 2024 Feb 20;25(5):2464. doi: 10.3390/ijms25052464.
10
miR-184 represses β-catenin and behaves as a skin tumor suppressor.miR-184 抑制β-catenin 并表现为皮肤肿瘤抑制因子。
Cell Death Dis. 2024 Feb 26;15(2):174. doi: 10.1038/s41419-024-06554-4.

本文引用的文献

1
Astrocytic tumors.星形细胞瘤
Recent Results Cancer Res. 2009;171:3-24. doi: 10.1007/978-3-540-31206-2_1.
2
IDH1 and IDH2 mutations in gliomas.胶质瘤中的异柠檬酸脱氢酶1(IDH1)和异柠檬酸脱氢酶2(IDH2)突变
N Engl J Med. 2009 Feb 19;360(8):765-73. doi: 10.1056/NEJMoa0808710.
3
MicroRNA regulation of a cancer network: consequences of the feedback loops involving miR-17-92, E2F, and Myc.微小RNA对癌症网络的调控:涉及miR-17-92、E2F和Myc的反馈回路的影响
Proc Natl Acad Sci U S A. 2008 Dec 16;105(50):19678-83. doi: 10.1073/pnas.0811166106. Epub 2008 Dec 9.
4
MicroRNA-184 antagonizes microRNA-205 to maintain SHIP2 levels in epithelia.微小RNA-184拮抗微小RNA-205以维持上皮细胞中SHIP2的水平。
Proc Natl Acad Sci U S A. 2008 Dec 9;105(49):19300-5. doi: 10.1073/pnas.0803992105. Epub 2008 Nov 25.
5
Targeting of the Bmi-1 oncogene/stem cell renewal factor by microRNA-128 inhibits glioma proliferation and self-renewal.微小RNA-128靶向Bmi-1癌基因/干细胞更新因子可抑制神经胶质瘤的增殖和自我更新。
Cancer Res. 2008 Nov 15;68(22):9125-30. doi: 10.1158/0008-5472.CAN-08-2629.
6
MicroRNA-298 and microRNA-328 regulate expression of mouse beta-amyloid precursor protein-converting enzyme 1.微小RNA-298和微小RNA-328调节小鼠β-淀粉样前体蛋白转化酶1的表达。
J Biol Chem. 2009 Jan 23;284(4):1971-81. doi: 10.1074/jbc.M807530200. Epub 2008 Nov 5.
7
Analysis of the IDH1 codon 132 mutation in brain tumors.脑肿瘤中异柠檬酸脱氢酶1(IDH1)第132位密码子突变的分析。
Acta Neuropathol. 2008 Dec;116(6):597-602. doi: 10.1007/s00401-008-0455-2. Epub 2008 Nov 5.
8
miR-296 regulates growth factor receptor overexpression in angiogenic endothelial cells.微小RNA-296调控血管生成性内皮细胞中生长因子受体的过表达。
Cancer Cell. 2008 Nov 4;14(5):382-93. doi: 10.1016/j.ccr.2008.10.005.
9
MicroRNA-21 targets a network of key tumor-suppressive pathways in glioblastoma cells.微小RNA-21靶向胶质母细胞瘤细胞中关键的肿瘤抑制通路网络。
Cancer Res. 2008 Oct 1;68(19):8164-72. doi: 10.1158/0008-5472.CAN-08-1305.
10
MicroRNAs in cancer.癌症中的微小RNA
Annu Rev Pathol. 2009;4:199-227. doi: 10.1146/annurev.pathol.4.110807.092222.