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胶质母细胞瘤生物学与治疗的微观掌控者:微小RNA日益凸显的作用

Micro-masters of glioblastoma biology and therapy: increasingly recognized roles for microRNAs.

作者信息

Floyd Desiree, Purow Benjamin

机构信息

Neurology Department, University of Virginia, Charlottesville, Virginia (D.F. and B.P.).

出版信息

Neuro Oncol. 2014 May;16(5):622-7. doi: 10.1093/neuonc/nou049. Epub 2014 Apr 10.

DOI:10.1093/neuonc/nou049
PMID:24723563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3984565/
Abstract

MicroRNAs are small noncoding RNAs encoded in eukaryotic genomes that have been found to play critical roles in most biological processes, including cancer. This is true for glioblastoma, the most common and lethal primary brain tumor, for which microRNAs have been shown to strongly influence cell viability, stem cell characteristics, invasiveness, angiogenesis, metabolism, and immune evasion. Developing microRNAs as prognostic markers or as therapeutic agents is showing increasing promise and has potential to reach the clinic in the next several years. This succinct review summarizes current progress and future directions in this exciting and steadily expanding field.

摘要

微小RNA是真核生物基因组中编码的小非编码RNA,已发现其在包括癌症在内的大多数生物学过程中发挥关键作用。胶质母细胞瘤是最常见且致命的原发性脑肿瘤,情况亦是如此,微小RNA已被证明对其细胞活力、干细胞特性、侵袭性、血管生成、代谢和免疫逃逸有强烈影响。将微小RNA开发为预后标志物或治疗剂显示出越来越大的前景,并且有可能在未来几年进入临床。这篇简要综述总结了这个令人兴奋且不断发展的领域的当前进展和未来方向。

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Micro-masters of glioblastoma biology and therapy: increasingly recognized roles for microRNAs.胶质母细胞瘤生物学与治疗的微观掌控者:微小RNA日益凸显的作用
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本文引用的文献

1
microRNA-148a is a prognostic oncomiR that targets MIG6 and BIM to regulate EGFR and apoptosis in glioblastoma.微小 RNA-148a 是一种预后致癌 miRNA,它靶向 MIG6 和 BIM 来调节胶质母细胞瘤中的 EGFR 和细胞凋亡。
Cancer Res. 2014 Mar 1;74(5):1541-53. doi: 10.1158/0008-5472.CAN-13-1449. Epub 2014 Jan 14.
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miR-218 opposes a critical RTK-HIF pathway in mesenchymal glioblastoma.miR-218 拮抗间充质胶质母细胞瘤中关键的 RTK-HIF 通路。
Proc Natl Acad Sci U S A. 2014 Jan 7;111(1):291-6. doi: 10.1073/pnas.1314341111. Epub 2013 Dec 24.
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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.
4
MiR-21 in the extracellular vesicles (EVs) of cerebrospinal fluid (CSF): a platform for glioblastoma biomarker development.脑脊液(CSF)细胞外囊泡(EVs)中的MiR-21:胶质母细胞瘤生物标志物开发的一个平台
PLoS One. 2013 Oct 21;8(10):e78115. doi: 10.1371/journal.pone.0078115. eCollection 2013.
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A miR-297/hypoxia/DGK-α axis regulating glioblastoma survival.miR-297/缺氧/DGK-α 轴调控脑胶质母细胞瘤的存活。
Neuro Oncol. 2013 Dec;15(12):1652-63. doi: 10.1093/neuonc/not118. Epub 2013 Oct 24.
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A high Notch pathway activation predicts response to γ secretase inhibitors in proneural subtype of glioma tumor-initiating cells.Notch信号通路的高度激活预示着神经胶质瘤肿瘤起始细胞的神经干细胞样亚型对γ分泌酶抑制剂的反应。
Stem Cells. 2014 Jan;32(1):301-12. doi: 10.1002/stem.1528.
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LIN28A facilitates the transformation of human neural stem cells and promotes glioblastoma tumorigenesis through a pro-invasive genetic program.LIN28A通过一个促侵袭性遗传程序促进人类神经干细胞的转化并推动胶质母细胞瘤的肿瘤发生。
Oncotarget. 2013 Jul;4(7):1050-64. doi: 10.18632/oncotarget.1131.
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Glioma microvesicles carry selectively packaged coding and non-coding RNAs which alter gene expression in recipient cells.神经胶质瘤微囊泡携带选择性包装的编码和非编码 RNA,改变受体细胞中的基因表达。
RNA Biol. 2013 Aug;10(8):1333-44. doi: 10.4161/rna.25281. Epub 2013 Jun 17.
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MicroRNA-137 is downregulated in glioblastoma and inhibits the stemness of glioma stem cells by targeting RTVP-1.微小RNA-137在胶质母细胞瘤中表达下调,并通过靶向RTVP-1抑制胶质瘤干细胞的干性。
Oncotarget. 2013 May;4(5):665-76. doi: 10.18632/oncotarget.928.
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miR-124 inhibits STAT3 signaling to enhance T cell-mediated immune clearance of glioma.miR-124 抑制 STAT3 信号通路以增强 T 细胞介导的胶质母细胞瘤免疫清除作用。
Cancer Res. 2013 Jul 1;73(13):3913-26. doi: 10.1158/0008-5472.CAN-12-4318. Epub 2013 May 1.