• 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

微小RNA-137:人类胶质瘤的新型治疗靶点

miR-137: A Novel Therapeutic Target for Human Glioma.

作者信息

Wang Yajun, Chen Riling, Zhou Xia, Guo Runmin, Yin Jingwen, Li You, Ma Guoda

机构信息

Maternal and Children's Health Research Institute, Shunde Women and Children's Hospital, Guangdong Medical University, Foshan 528300, China; Clinical Research Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, China; Wolfson Institute for Biomedical Research, University College London, London WC1E 6BT, UK.

Maternal and Children's Health Research Institute, Shunde Women and Children's Hospital, Guangdong Medical University, Foshan 528300, China.

出版信息

Mol Ther Nucleic Acids. 2020 Sep 4;21:614-622. doi: 10.1016/j.omtn.2020.06.028. Epub 2020 Jun 30.

DOI:10.1016/j.omtn.2020.06.028
PMID:32736290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7393316/
Abstract

MicroRNA (miR)-137 is highly expressed in the brain and plays a crucial role in the development and prognosis of glioma. In this review, we aim to summarize the latest findings regarding miR-137 in glioma cell apoptosis, proliferation, migration, invasion, angiogenesis, drug resistance, and cancer treatment. In addition, we focus on the identified miR-137 targets and pathways in the occurrence and development of glioma. Finally, future implications for the diagnostic and therapeutic potential of miR-137 in glioma were discussed.

摘要

微小RNA(miR)-137在大脑中高度表达,在胶质瘤的发生发展和预后中起关键作用。在本综述中,我们旨在总结关于miR-137在胶质瘤细胞凋亡、增殖、迁移、侵袭、血管生成、耐药性及癌症治疗方面的最新研究结果。此外,我们重点关注已确定的miR-137在胶质瘤发生发展中的靶点和信号通路。最后,讨论了miR-137在胶质瘤诊断和治疗潜力方面的未来意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c00f/7393316/636908a0a512/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c00f/7393316/39fc9a29296d/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c00f/7393316/54d5624c0ec3/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c00f/7393316/636908a0a512/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c00f/7393316/39fc9a29296d/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c00f/7393316/54d5624c0ec3/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c00f/7393316/636908a0a512/gr2.jpg

相似文献

1
miR-137: A Novel Therapeutic Target for Human Glioma.微小RNA-137:人类胶质瘤的新型治疗靶点
Mol Ther Nucleic Acids. 2020 Sep 4;21:614-622. doi: 10.1016/j.omtn.2020.06.028. Epub 2020 Jun 30.
2
Upregulation of microRNA-133a and downregulation of connective tissue growth factor suppress cell proliferation, migration, and invasion in human glioma through the JAK/STAT signaling pathway.microRNA-133a 的上调和结缔组织生长因子的下调通过 JAK/STAT 信号通路抑制人胶质瘤细胞的增殖、迁移和侵袭。
IUBMB Life. 2019 Dec;71(12):1857-1875. doi: 10.1002/iub.2126. Epub 2019 Aug 5.
3
MicroRNA-302a targets GAB2 to suppress cell proliferation, migration and invasion of glioma.微小RNA-302a靶向衔接蛋白生长因子受体结合蛋白2以抑制神经胶质瘤细胞的增殖、迁移和侵袭。
Oncol Rep. 2017 Feb;37(2):1159-1167. doi: 10.3892/or.2016.5320. Epub 2016 Dec 15.
4
MicroRNA-101 inhibits proliferation, migration and invasion of human glioblastoma by targeting SOX9.微小RNA-101通过靶向SOX9抑制人胶质母细胞瘤的增殖、迁移和侵袭。
Oncotarget. 2017 Mar 21;8(12):19244-19254. doi: 10.18632/oncotarget.13706.
5
miR-423-5p contributes to a malignant phenotype and temozolomide chemoresistance in glioblastomas.miR-423-5p促成胶质母细胞瘤的恶性表型和替莫唑胺化疗耐药性。
Neuro Oncol. 2017 Jan;19(1):55-65. doi: 10.1093/neuonc/now129. Epub 2016 Jul 28.
6
Anti-miRNA-23a oligonucleotide suppresses glioma cells growth by targeting apoptotic protease activating factor-1.反义 miR-23a 寡核苷酸通过靶向凋亡蛋白酶激活因子-1 抑制神经胶质瘤细胞生长。
Curr Pharm Des. 2013;19(35):6382-9. doi: 10.2174/13816128113199990509.
7
Suppression of miR-221 inhibits glioma cells proliferation and invasion via targeting SEMA3B.miR-221的抑制通过靶向SEMA3B抑制胶质瘤细胞的增殖和侵袭。
Biol Res. 2015 Jul 22;48(1):37. doi: 10.1186/s40659-015-0030-y.
8
MicroRNA-544 inhibits glioma proliferation, invasion and migration but induces cell apoptosis by targeting PARK7.微小RNA-544通过靶向PARK7抑制神经胶质瘤的增殖、侵袭和迁移,但诱导细胞凋亡。
Am J Transl Res. 2016 Apr 15;8(4):1826-37. eCollection 2016.
9
MicroRNA-144: A novel biological marker and potential therapeutic target in human solid cancers.微小RNA-144:人类实体癌中的一种新型生物标志物及潜在治疗靶点。
J Cancer. 2020 Sep 25;11(22):6716-6726. doi: 10.7150/jca.46293. eCollection 2020.
10
MiR-16-1 plays a role in reducing migration and invasion of glioma cells.miR-16-1 在减少神经胶质瘤细胞迁移和侵袭中发挥作用。
Anat Rec (Hoboken). 2013 Mar;296(3):427-32. doi: 10.1002/ar.22626. Epub 2012 Nov 23.

引用本文的文献

1
Brain miR-137 governs growth and development via GH/IGF-1 signaling.大脑中的微小核糖核酸-137通过生长激素/胰岛素样生长因子-1信号通路调控生长与发育。
BMC Biol. 2025 Jul 1;23(1):197. doi: 10.1186/s12915-025-02306-8.
2
miR-137: A therapeutic candidate or a key molecular regulator in Alzheimer's disease?微小RNA-137:阿尔茨海默病的一种治疗候选物还是关键分子调节因子?
J Alzheimers Dis Rep. 2025 Jun 25;9:25424823251352166. doi: 10.1177/25424823251352166. eCollection 2025 Jan-Dec.
3
miR-137 targets Myc to regulate growth during eye development.微小RNA-137靶向Myc以调控眼睛发育过程中的生长。

本文引用的文献

1
Histone Modifying Enzymes and Chromatin Modifiers in Glioma Pathobiology and Therapy Responses.组蛋白修饰酶和染色质修饰因子在神经胶质瘤病理生物学和治疗反应中的作用
Adv Exp Med Biol. 2020;1202:259-279. doi: 10.1007/978-3-030-30651-9_13.
2
MiRNA-137-mediated modulation of mitochondrial dynamics regulates human neural stem cell fate.miRNA-137 介导的线粒体动态调节调控人神经干细胞命运。
Stem Cells. 2020 May;38(5):683-697. doi: 10.1002/stem.3155. Epub 2020 Feb 8.
3
Knockdown Of lncRNA NCK-AS1 Regulates Cisplatin Resistance Through Modulating miR-137 In Osteosarcoma Cells.
Development. 2025 Jul 15;152(14). doi: 10.1242/dev.204373. Epub 2025 Jul 16.
4
Nanomedicines Targeting Metabolic Pathways in the Tumor Microenvironment: Future Perspectives and the Role of AI.靶向肿瘤微环境中代谢途径的纳米药物:未来展望与人工智能的作用
Metabolites. 2025 Mar 13;15(3):201. doi: 10.3390/metabo15030201.
5
The role of miR-152 in urological tumors: potential biomarkers and therapeutic targets.miR-152 在尿路上皮肿瘤中的作用:潜在的生物标志物和治疗靶点。
Front Immunol. 2024 Nov 13;15:1464327. doi: 10.3389/fimmu.2024.1464327. eCollection 2024.
6
miR-137: a potential therapeutic target for lung cancer.微小RNA-137:肺癌的潜在治疗靶点
Front Cell Dev Biol. 2024 Aug 23;12:1427724. doi: 10.3389/fcell.2024.1427724. eCollection 2024.
7
Emerging Insights into the PI3K/AKT/mTOR Signaling Pathway and Non-Coding RNA-mediated Drug Resistance in Glioblastoma.胶质母细胞瘤中PI3K/AKT/mTOR信号通路及非编码RNA介导的耐药性的新见解
Curr Mol Med. 2025;25(6):710-722. doi: 10.2174/0115665240309647240516042716.
8
MiR-128-3p - a gray eminence of the human central nervous system.微小RNA-128-3p——人类中枢神经系统的一个无名小卒。
Mol Ther Nucleic Acids. 2024 Feb 6;35(1):102141. doi: 10.1016/j.omtn.2024.102141. eCollection 2024 Mar 12.
9
Early-Stage Application of Agomir-137 Promotes Locomotor Recovery in a Mouse Model of Motor Cortex Injury.Agomir-137 的早期应用促进运动皮层损伤小鼠模型运动功能恢复。
Int J Mol Sci. 2023 Dec 5;24(24):17156. doi: 10.3390/ijms242417156.
10
microRNAs (miRNAs) in Glioblastoma Multiforme (GBM)-Recent Literature Review.多形性胶质母细胞瘤(GBM)中的微小RNA(miRNA)——近期文献综述
Int J Mol Sci. 2023 Feb 9;24(4):3521. doi: 10.3390/ijms24043521.
lncRNA NCK-AS1的敲低通过调节骨肉瘤细胞中的miR-137来调控顺铂耐药性。
Onco Targets Ther. 2019 Dec 16;12:11057-11068. doi: 10.2147/OTT.S228199. eCollection 2019.
4
Over-expression of long noncoding RNA HOTAIRM1 promotes cell proliferation and invasion in human glioblastoma by up-regulating SP1 via sponging miR-137.长链非编码 RNA HOTAIRM1 通过海绵吸附 miR-137 上调 SP1 促进人脑胶质瘤细胞增殖和侵袭。
Neuroreport. 2020 Jan 27;31(2):109-117. doi: 10.1097/WNR.0000000000001380.
5
miR-137 alleviates doxorubicin resistance in breast cancer through inhibition of epithelial-mesenchymal transition by targeting DUSP4.miR-137 通过靶向 DUSP4 抑制上皮-间充质转化缓解乳腺癌多柔比星耐药。
Cell Death Dis. 2019 Dec 4;10(12):922. doi: 10.1038/s41419-019-2164-2.
6
NCK1-AS1 Increases Drug Resistance of Glioma Cells to Temozolomide by Modulating miR-137/.NCK1-AS1 通过调节 miR-137/ 增加胶质瘤细胞对替莫唑胺的耐药性。
Cancer Biother Radiopharm. 2020 Mar;35(2):101-108. doi: 10.1089/cbr.2019.3054. Epub 2019 Nov 21.
7
A VNTR Regulates miR-137 Expression Through Novel Alternative Splicing and Contributes to Risk for Schizophrenia.VNTR 通过新型可变剪接调控 miR-137 的表达,并导致精神分裂症的发病风险增加。
Sci Rep. 2019 Aug 13;9(1):11793. doi: 10.1038/s41598-019-48141-0.
8
Serum secreted miR-137-containing exosomes affects oxidative stress of neurons by regulating OXR1 in Parkinson's disease.血清分泌的含有 miR-137 的外泌体通过调节帕金森病中的 OXR1 影响神经元的氧化应激。
Brain Res. 2019 Nov 1;1722:146331. doi: 10.1016/j.brainres.2019.146331. Epub 2019 Jul 10.
9
Epigenetic silencing of miR-137 induces resistance to bicalutamide by targeting TRIM24 in prostate cancer cells.miR-137的表观遗传沉默通过靶向前列腺癌细胞中的TRIM24诱导对比卡鲁胺的抗性。
Am J Transl Res. 2019 May 15;11(5):3226-3237. eCollection 2019.
10
Overexpression of mircoRNA-137 inhibits cervical cancer cell invasion, migration and epithelial-mesenchymal transition by suppressing the TGF-β/smad pathway via binding to GREM1.微小RNA-137的过表达通过与GREM1结合抑制TGF-β/smad信号通路,从而抑制宫颈癌细胞的侵袭、迁移和上皮-间质转化。
Cancer Cell Int. 2019 May 23;19:147. doi: 10.1186/s12935-019-0852-8. eCollection 2019.