• 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

相似文献

1
Potential role of miRNAs and their inhibitors in glioma treatment.miRNAs 及其抑制剂在神经胶质瘤治疗中的潜在作用。
Expert Rev Anticancer Ther. 2010 Nov;10(11):1753-62. doi: 10.1586/era.10.168.
2
miRNA Regulation in Gliomas: Usual Suspects in Glial Tumorigenesis and Evolving Clinical Applications.胶质瘤中的miRNA调控:胶质肿瘤发生中的常见因素及不断发展的临床应用
J Neuropathol Exp Neurol. 2017 Apr 1;76(4):246-254. doi: 10.1093/jnen/nlx005.
3
[New glioma therapy using specific microRNAs].[使用特定微小RNA的新型神经胶质瘤疗法]
Ugeskr Laeger. 2012 Mar 5;174(10):630-3.
4
miR-6858 plays a key role in the process of melatonin inhibition of the malignant biological behavior of glioma.miR-6858 在褪黑素抑制神经胶质瘤恶性生物学行为的过程中发挥关键作用。
J Clin Neurosci. 2021 May;87:137-146. doi: 10.1016/j.jocn.2021.02.015. Epub 2021 Mar 20.
5
Dynamics of circulating hypoxia-mediated miRNAs and tumor response in patients with high-grade glioma treated with bevacizumab.缺氧相关循环 miRNA 动力学与贝伐珠单抗治疗高级别脑胶质瘤患者的肿瘤应答
J Neurosurg. 2016 Oct;125(4):1008-1015. doi: 10.3171/2015.8.JNS15437. Epub 2016 Jan 22.
6
Emerging functions of microRNAs in glioblastoma.微小RNA在胶质母细胞瘤中的新功能
J Neurooncol. 2009 May;92(3):297-306. doi: 10.1007/s11060-009-9843-2. Epub 2009 Apr 9.
7
A restricted signature of serum miRNAs distinguishes glioblastoma from lower grade gliomas.血清微小RNA的受限特征可区分胶质母细胞瘤与低级别胶质瘤。
J Exp Clin Cancer Res. 2016 Jul 30;35(1):124. doi: 10.1186/s13046-016-0393-0.
8
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.
9
Role of micro-RNA (miRNA) in pathogenesis of glioblastoma.微小RNA(miRNA)在胶质母细胞瘤发病机制中的作用。
Eur Rev Med Pharmacol Sci. 2015;19(9):1630-9.
10
Glioma angiogenesis: Towards novel RNA therapeutics.胶质瘤血管生成:迈向新型RNA疗法。
Cell Adh Migr. 2009 Apr-Jun;3(2):230-5. doi: 10.4161/cam.3.2.7910. Epub 2009 Apr 22.

引用本文的文献

1
MiR-95-3p acts as a prognostic marker and promotes cervical cancer progression by targeting VCAM1.微小RNA-95-3p作为一种预后标志物,通过靶向血管细胞黏附分子1促进宫颈癌进展。
Ann Transl Med. 2022 Nov;10(21):1171. doi: 10.21037/atm-22-5184.
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
A 4-miRNA signature predicts the therapeutic outcome of glioblastoma.一种4-微RNA特征可预测胶质母细胞瘤的治疗结果。
Oncotarget. 2016 Jul 19;7(29):45764-45775. doi: 10.18632/oncotarget.9945.
4
High expression of CXCR3 is an independent prognostic factor in glioblastoma patients that promotes an invasive phenotype.CXCR3的高表达是胶质母细胞瘤患者的一个独立预后因素,可促进侵袭性表型。
J Neurooncol. 2015 Mar;122(1):43-51. doi: 10.1007/s11060-014-1692-y. Epub 2014 Dec 20.
5
Leveraging metabolomics to assess the next generation of temozolomide-based therapeutic approaches for glioblastomas.利用代谢组学评估新一代基于替莫唑胺的胶质母细胞瘤治疗方法。
Genomics Proteomics Bioinformatics. 2013 Aug;11(4):199-206. doi: 10.1016/j.gpb.2013.04.003. Epub 2013 Jun 1.
6
Direct quantification of microRNA at low picomolar level in sera of glioma patients using a competitive hybridization followed by amplified voltammetric detection.利用竞争性杂交和放大伏安检测技术在胶质瘤患者血清中直接定量检测皮摩尔级别的 microRNA。
Anal Chem. 2012 Aug 7;84(15):6400-6. doi: 10.1021/ac203368h. Epub 2012 Jul 10.
7
miRNA expression profiling in migrating glioblastoma cells: regulation of cell migration and invasion by miR-23b via targeting of Pyk2.miRNA 表达谱在迁移性脑胶质瘤细胞中的研究:miR-23b 通过靶向 Pyk2 调控细胞迁移和侵袭。
PLoS One. 2012;7(6):e39818. doi: 10.1371/journal.pone.0039818. Epub 2012 Jun 22.
8
Genome-wide profiling identified a set of miRNAs that are differentially expressed in glioblastoma stem cells and normal neural stem cells.全基因组谱分析鉴定出一组在神经胶质瘤干细胞和正常神经干细胞中差异表达的 miRNAs。
PLoS One. 2012;7(4):e36248. doi: 10.1371/journal.pone.0036248. Epub 2012 Apr 30.
9
miRNA-mediated immune regulation and immunotherapeutic potential in glioblastoma.微小RNA介导的胶质母细胞瘤免疫调节及免疫治疗潜力
Clin Investig (Lond). 2011 Dec;1(12):1637-1650. doi: 10.4155/cli.11.159.
10
Recent advances in the molecular understanding of glioblastoma.胶质母细胞瘤的分子研究进展。
J Neurooncol. 2012 May;108(1):11-27. doi: 10.1007/s11060-011-0793-0. Epub 2012 Jan 20.

本文引用的文献

1
MicroRNA-181 family predicts response to concomitant chemoradiotherapy with temozolomide in glioblastoma patients.微小 RNA-181 家族预测胶质母细胞瘤患者接受替莫唑胺同步放化疗的反应。
Neoplasma. 2010;57(3):264-9. doi: 10.4149/neo_2010_03_264.
2
MicroRNA-451 regulates LKB1/AMPK signaling and allows adaptation to metabolic stress in glioma cells.microRNA-451 调节 LKB1/AMPK 信号通路并允许神经胶质瘤细胞适应代谢应激。
Mol Cell. 2010 Mar 12;37(5):620-32. doi: 10.1016/j.molcel.2010.02.018.
3
microRNA-34a is tumor suppressive in brain tumors and glioma stem cells.miRNA-34a 在脑肿瘤和神经胶质瘤干细胞中具有肿瘤抑制作用。
Cell Cycle. 2010 Mar 15;9(6):1031-6. doi: 10.4161/cc.9.6.10987.
4
Integrative genome analysis reveals an oncomir/oncogene cluster regulating glioblastoma survivorship.整合基因组分析揭示了一个调节胶质母细胞瘤存活的 microRNA/oncogene 簇。
Proc Natl Acad Sci U S A. 2010 Feb 2;107(5):2183-8. doi: 10.1073/pnas.0909896107. Epub 2010 Jan 13.
5
The neuronal microRNA miR-326 acts in a feedback loop with notch and has therapeutic potential against brain tumors.神经元微小RNA miR-326与Notch形成反馈回路,并具有抗脑肿瘤的治疗潜力。
J Neurosci. 2009 Dec 2;29(48):15161-8. doi: 10.1523/JNEUROSCI.4966-09.2009.
6
Treatment of malignant gliomas with TGF-beta2 antisense oligonucleotides.用 TGF-β2 反义寡核苷酸治疗恶性神经胶质瘤。
Expert Rev Anticancer Ther. 2009 Nov;9(11):1663-74. doi: 10.1586/era.09.138.
7
Notch activity in the nervous system: to switch or not switch?神经系统中的 Notch 活性:开关还是不开关?
Neural Dev. 2009 Oct 2;4:36. doi: 10.1186/1749-8104-4-36.
8
MicroRNA-34a inhibits glioblastoma growth by targeting multiple oncogenes.微小RNA-34a通过靶向多个癌基因抑制胶质母细胞瘤的生长。
Cancer Res. 2009 Oct 1;69(19):7569-76. doi: 10.1158/0008-5472.CAN-09-0529. Epub 2009 Sep 22.
9
Systemic delivery of synthetic microRNA-16 inhibits the growth of metastatic prostate tumors via downregulation of multiple cell-cycle genes.系统递送合成 microRNA-16 通过下调多个细胞周期基因抑制转移性前列腺肿瘤的生长。
Mol Ther. 2010 Jan;18(1):181-7. doi: 10.1038/mt.2009.207. Epub 2009 Sep 8.
10
Exploiting and antagonizing microRNA regulation for therapeutic and experimental applications.利用和拮抗微小RNA调控以用于治疗和实验应用。
Nat Rev Genet. 2009 Aug;10(8):578-85. doi: 10.1038/nrg2628.

miRNAs 及其抑制剂在神经胶质瘤治疗中的潜在作用。

Potential role of miRNAs and their inhibitors in glioma treatment.

机构信息

Department of Neurological Surgery, The Ohio State University Comprehensive Cancer Center, Wiseman Hall, 400 West 12th Avenue, Columbus, OH 43210, USA.

出版信息

Expert Rev Anticancer Ther. 2010 Nov;10(11):1753-62. doi: 10.1586/era.10.168.

DOI:10.1586/era.10.168
PMID:21080802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7330712/
Abstract

Recent years have seen an intense period of research on the functions of miRNAs, recently discovered key regulators of gene expression that act through suppression of translation of target mRNAs. Several hundred miRNAs have been identified in humans, and these show characteristic expression patterns, depending on tissue type, cell type or environmental stimuli. Like other types of cancer, the brain tumor glioblastoma shows a distinct miRNA expression signature, and a number of recent studies have linked these miRNA alterations to key hallmarks of glioblastoma including proliferation, survival, invasion, angiogenesis and stem cell-like behavior. These studies have opened the door to the possibility of utilizing miRNAs or miRNA antagonists as therapeutic agents for the treatment of brain tumors.

摘要

近年来,人们对 miRNA 的功能进行了深入研究,miRNA 是最近发现的基因表达关键调控因子,可以通过抑制靶 mRNA 的翻译来发挥作用。在人类中已经鉴定出数百种 miRNA,它们根据组织类型、细胞类型或环境刺激显示出特征性的表达模式。与其他类型的癌症一样,脑肿瘤胶质母细胞瘤表现出独特的 miRNA 表达特征,最近的一些研究将这些 miRNA 的改变与胶质母细胞瘤的关键特征联系起来,包括增殖、存活、侵袭、血管生成和干细胞样行为。这些研究为利用 miRNA 或 miRNA 拮抗剂作为脑肿瘤治疗的治疗剂开辟了可能性。