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微小 RNA 靶向治疗作为一种对抗神经胶质瘤的策略。

MicroRNA targeting as a therapeutic strategy against glioma.

机构信息

Brain Tumor Center, The University of Chicago, Chicago, IL 60637, USA.

出版信息

Curr Mol Med. 2013 May;13(4):535-42. doi: 10.2174/1566524011313040006.

DOI:10.2174/1566524011313040006
PMID:22934848
Abstract

Glioblastoma multiforme (GBM), the most common and aggressive form of primary brain tumor, presents a dismal prognosis. Current standard therapies are only able to improve patient survival by a few months. The search for alternative approaches in glioblastoma treatment, together with the recent discovery of a new class of small RNA molecules that are capable of regulating gene expression, prompted a race for a deeper and thorough understanding of how these molecules work. Today, it is known that microRNAs are involved in many cellular processes that are altered in GBM tumors, such as angiogenesis, invasion, cell proliferation and apoptosis. Research in this area is now gathering efforts to translate these findings into clinically relevant therapies that could improve the diagnosis and outcome of GBM patients. In this review, we discuss the use of microRNAs as potential diagnostic, prognostic and therapeutic tools against glioblastoma. We will also assess the current challenges and future perspectives of microRNA-based therapies, with a special focus on why this promising therapeutic approach is not yet in the clinic and how to overcome this limitation.

摘要

多形性胶质母细胞瘤(GBM)是最常见和侵袭性最强的原发性脑肿瘤,预后极差。目前的标准治疗方法只能使患者的生存时间延长几个月。为了寻找胶质母细胞瘤治疗的替代方法,以及最近发现一类能够调节基因表达的新型小分子 RNA 分子,人们竞相深入了解这些分子的作用机制。如今,人们已经知道 microRNAs 参与了 GBM 肿瘤中许多发生改变的细胞过程,如血管生成、侵袭、细胞增殖和细胞凋亡。该领域的研究目前正在努力将这些发现转化为具有临床意义的治疗方法,以改善 GBM 患者的诊断和预后。在这篇综述中,我们讨论了 microRNAs 作为针对胶质母细胞瘤的潜在诊断、预后和治疗工具的用途。我们还将评估基于 microRNA 的治疗方法的当前挑战和未来前景,特别关注为什么这种有前途的治疗方法尚未在临床上应用,以及如何克服这一限制。

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MicroRNA targeting as a therapeutic strategy against glioma.微小 RNA 靶向治疗作为一种对抗神经胶质瘤的策略。
Curr Mol Med. 2013 May;13(4):535-42. doi: 10.2174/1566524011313040006.
2
MicroRNAs in glioblastoma: role in pathogenesis and opportunities for targeted therapies.胶质母细胞瘤中的微小RNA:在发病机制中的作用及靶向治疗的机会
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MicroRNAs as Multifaceted Players in Glioblastoma Multiforme.微小 RNA 作为多形性胶质母细胞瘤的多面手。
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miRNA Multiplayers in glioma. From bench to bedside.胶质瘤中的微小RNA多面手。从实验室到临床。
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A three-microRNA signature identifies two subtypes of glioblastoma patients with different clinical outcomes.一个包含三个 microRNA 的特征可以将胶质母细胞瘤患者分为两种亚型,这两种亚型具有不同的临床结局。
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引用本文的文献

1
Recent insights into the microRNA-dependent modulation of gliomas from pathogenesis to diagnosis and treatment.从发病机制到诊断和治疗,深入了解 microRNA 调控胶质瘤的最新研究进展。
Cell Mol Biol Lett. 2022 Aug 3;27(1):65. doi: 10.1186/s11658-022-00354-4.
2
MicroRNA-585 inhibits human glioma cell proliferation by directly targeting MDM2.微小RNA-585通过直接靶向MDM2抑制人胶质瘤细胞增殖。
Cancer Cell Int. 2020 Sep 29;20:469. doi: 10.1186/s12935-020-01528-w. eCollection 2020.
3
The Role of miRNAs in Angiogenesis, Invasion and Metabolism and Their Therapeutic Implications in Gliomas.
微小RNA在血管生成、侵袭和代谢中的作用及其在胶质瘤治疗中的意义
Cancers (Basel). 2017 Jul 10;9(7):85. doi: 10.3390/cancers9070085.
4
MicroRNA-98 Attenuates Cell Migration and Invasion in Glioma by Directly Targeting Pre-B Cell Leukemia Homeobox 3.微小 RNA-98 通过直接靶向 Pre-B 细胞白血病同源盒 3 来抑制神经胶质瘤细胞的迁移和侵袭。
Cell Mol Neurobiol. 2017 Nov;37(8):1359-1371. doi: 10.1007/s10571-017-0466-4. Epub 2017 Jan 25.
5
MicroRNA-93 promotes the malignant phenotypes of human glioma cells and induces their chemoresistance to temozolomide.微小RNA-93促进人胶质瘤细胞的恶性表型并诱导其对替莫唑胺的化学抗性。
Biol Open. 2016 Jun 15;5(6):669-77. doi: 10.1242/bio.015552.
6
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.
7
HOTAIR is a therapeutic target in glioblastoma.HOTAIR是胶质母细胞瘤的一个治疗靶点。
Oncotarget. 2015 Apr 10;6(10):8353-65. doi: 10.18632/oncotarget.3229.
8
Serum microRNA-210 as a potential noninvasive biomarker for the diagnosis and prognosis of glioma.血清微小RNA-210作为胶质瘤诊断和预后的潜在非侵入性生物标志物。
Br J Cancer. 2015 Mar 31;112(7):1241-6. doi: 10.1038/bjc.2015.91.
9
MiR-15b targets cyclin D1 to regulate proliferation and apoptosis in glioma cells.微小RNA-15b靶向细胞周期蛋白D1以调节胶质瘤细胞的增殖和凋亡。
Biomed Res Int. 2014;2014:687826. doi: 10.1155/2014/687826. Epub 2014 Jun 4.
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MicroRNA-566 activates EGFR signaling and its inhibition sensitizes glioblastoma cells to nimotuzumab.微小RNA-566激活表皮生长因子受体信号通路,抑制该因子可使胶质母细胞瘤细胞对尼妥珠单抗敏感。
Mol Cancer. 2014 Mar 20;13:63. doi: 10.1186/1476-4598-13-63.