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Notch 信号通路与 microRNA:神经发生与胶质母细胞瘤之间的动态双重调控。

Notch Signaling and MicroRNA: The Dynamic Duo Steering Between Neurogenesis and Glioblastomas.

机构信息

Office of Research Innovation and Commercialization Department, Lahore Garrison University, Lahore, Pakistan.

Atta-ur-Rahman School of Applied Biosciences (ASAB), National University of Sciences and Technology (NUST), H-12, Islamabad 44000, Pakistan.

出版信息

Cell Mol Biol (Noisy-le-grand). 2021 Aug 15;67(2):33-43. doi: 10.14715/cmb/2021.67.2.6.

DOI:10.14715/cmb/2021.67.2.6
PMID:34817376
Abstract

Notch signaling is an evolutionary conserved pathway that plays a central role in development and differentiation of eukaryotic cells. It has been well documented that Notch signaling is inevitable for neuronal cell growth and homeostasis. It regulates process of differentiation from early embryonic stages to fully developed brain. To achieve this streamlined development of neuronal cells, a number of cellular processes are being orchestrated by the Notch signaling. Abrogated Notch signaling is related to several brain tumors, including glioblastomas. On the other hand, microRNAs are small molecules that play decisive role in mediating and modulating Notch signaling. This review discusses the crucial role of Notch signaling in development of nervous system and how this versatile pathway interplay with microRNAs in glioblastoma. This review sheds light on interplay between abrogated Notch signaling and miRNAs in the regulation of neuronal differentiation with special focus on miRNAs mediated regulation of tumorigenesis in glioblastoma. Furthermore, it discusses different aspects of neurogenesis modulated by the Notch signaling that could be exploited for the identification of new diagnostic tools and therapies for the treatment of glioblastoma.

摘要

Notch 信号通路是一种进化上保守的途径,在真核细胞的发育和分化中起着核心作用。已有充分的文献证明,Notch 信号通路对于神经元细胞的生长和稳态是必不可少的。它调节着从早期胚胎阶段到完全发育的大脑的分化过程。为了实现神经元细胞的这种流线型发育,许多细胞过程都由 Notch 信号通路来协调。Notch 信号通路的中断与包括神经胶质瘤在内的几种脑瘤有关。另一方面,microRNAs 是在介导和调节 Notch 信号通路中起决定性作用的小分子。这篇综述讨论了 Notch 信号通路在神经系统发育中的关键作用,以及这种多功能通路如何与神经胶质瘤中的 microRNAs 相互作用。这篇综述阐明了 Notch 信号通路中断和 microRNAs 在神经元分化调节中的相互作用,特别关注 microRNAs 介导的神经胶质瘤中的肿瘤发生的调节。此外,它还讨论了 Notch 信号通路调节的神经发生的不同方面,可以利用这些方面来识别新的诊断工具和治疗神经胶质瘤的方法。

相似文献

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Notch Signaling and MicroRNA: The Dynamic Duo Steering Between Neurogenesis and Glioblastomas.Notch 信号通路与 microRNA:神经发生与胶质母细胞瘤之间的动态双重调控。
Cell Mol Biol (Noisy-le-grand). 2021 Aug 15;67(2):33-43. doi: 10.14715/cmb/2021.67.2.6.
2
Downregulation of RND3/RhoE in glioblastoma patients promotes tumorigenesis through augmentation of notch transcriptional complex activity.胶质母细胞瘤患者中RND3/RhoE的下调通过增强Notch转录复合体活性促进肿瘤发生。
Cancer Med. 2015 Sep;4(9):1404-16. doi: 10.1002/cam4.484. Epub 2015 Jun 24.
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Non-coding RNAs as Key Regulators of the Notch Signaling Pathway in Glioblastoma: Diagnostic, Prognostic, and Therapeutic Targets.非编码 RNA 作为胶质母细胞瘤 Notch 信号通路的关键调控因子:诊断、预后和治疗靶点。
CNS Neurol Disord Drug Targets. 2024;23(10):1203-1216. doi: 10.2174/0118715273277458231213063147.
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Deltex-1 activates mitotic signaling and proliferation and increases the clonogenic and invasive potential of U373 and LN18 glioblastoma cells and correlates with patient survival.Deltex-1 激活有丝分裂信号和增殖,增加 U373 和 LN18 胶质母细胞瘤细胞的克隆形成和侵袭潜能,并与患者生存相关。
PLoS One. 2013;8(2):e57793. doi: 10.1371/journal.pone.0057793. Epub 2013 Feb 25.
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MiR-134 regulates the proliferation and invasion of glioblastoma cells by reducing Nanog expression.miR-134 通过降低 Nanog 表达水平来调节神经胶质瘤细胞的增殖和侵袭。
Int J Oncol. 2013 May;42(5):1533-40. doi: 10.3892/ijo.2013.1844. Epub 2013 Mar 4.
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MicroRNA profiling in subventricular zone after stroke: MiR-124a regulates proliferation of neural progenitor cells through Notch signaling pathway.中风后侧脑室下区的 microRNA 谱分析:miR-124a 通过 Notch 信号通路调节神经祖细胞的增殖。
PLoS One. 2011;6(8):e23461. doi: 10.1371/journal.pone.0023461. Epub 2011 Aug 26.
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Notch Signaling & MicroRNAs - two tumblers of neurogenesis and Gliomas.Notch 信号通路与 microRNAs——神经发生与神经胶质瘤的两把“双刃剑”。
J Pak Med Assoc. 2021 Jan;71(1(B)):310-318. doi: 10.47391/JPMA.339.
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Inhibition of Notch signaling alters the phenotype of orthotopic tumors formed from glioblastoma multiforme neurosphere cells but does not hamper intracranial tumor growth regardless of endogene Notch pathway signature.抑制 Notch 信号通路会改变多形性胶质母细胞瘤神经球细胞形成的原位肿瘤的表型,但无论内源性 Notch 途径特征如何,都不会阻碍颅内肿瘤的生长。
Cancer Biol Ther. 2014 Jul;15(7):862-77. doi: 10.4161/cbt.28876. Epub 2014 Apr 22.
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CRMP5 Controls Glioblastoma Cell Proliferation and Survival through Notch-Dependent Signaling.CRMP5 通过 Notch 依赖性信号通路控制神经胶质瘤细胞的增殖和存活。
Cancer Res. 2015 Sep 1;75(17):3519-28. doi: 10.1158/0008-5472.CAN-14-0631. Epub 2015 Jun 29.
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Constitutive activation of signal transducer and activator of transcription 3 (STAT3) and nuclear factor κB signaling in glioblastoma cancer stem cells regulates the Notch pathway.胶质母细胞瘤肿瘤干细胞中信号转导子和转录激活子 3(STAT3)和核因子 κB 信号的组成性激活调节 Notch 通路。
J Biol Chem. 2013 Sep 6;288(36):26167-26176. doi: 10.1074/jbc.M113.477950. Epub 2013 Jul 31.

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Noncoding RNA Res. 2024 Jun 6;9(4):1292-1307. doi: 10.1016/j.ncrna.2024.06.006. eCollection 2024 Dec.
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Peptide ARHGEF9 Inhibits Glioma Progression via PI3K/AKT/mTOR Pathway.肽 ARHGEF9 通过 PI3K/AKT/mTOR 通路抑制神经胶质瘤进展。
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Serial Gene Expression Profiling of Neural Stem Cells Shows Transcriptome Switch by Long-Term Physioxia from Metabolic Adaption to Cell Signaling Profile.
神经干细胞的连续基因表达谱分析显示,长期生理性低氧会导致转录组从代谢适应转变为细胞信号谱。
Stem Cells Int. 2022 Nov 12;2022:6718640. doi: 10.1155/2022/6718640. eCollection 2022.