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本文引用的文献

1
microRNAs as cancer therapeutics: A step closer to clinical application.微小 RNA 作为癌症治疗药物:向临床应用迈进了一步。
Cancer Lett. 2017 Oct 28;407:113-122. doi: 10.1016/j.canlet.2017.04.007. Epub 2017 Apr 12.
2
Identification of microRNAs associated with glioma diagnosis and prognosis.与神经胶质瘤诊断和预后相关的微小RNA的鉴定。
Oncotarget. 2017 Apr 18;8(16):26394-26403. doi: 10.18632/oncotarget.14445.
3
Emerging role of microRNA-21 in cancer.微小RNA-21在癌症中的新兴作用。
Biomed Rep. 2016 Oct;5(4):395-402. doi: 10.3892/br.2016.747. Epub 2016 Aug 26.
4
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.
5
The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary.2016 年世界卫生组织中枢神经系统肿瘤分类:概述。
Acta Neuropathol. 2016 Jun;131(6):803-20. doi: 10.1007/s00401-016-1545-1. Epub 2016 May 9.
6
miR-15b and miR-21 as Circulating Biomarkers for Diagnosis of Glioma.miR-15b和miR-21作为诊断胶质瘤的循环生物标志物
Curr Genomics. 2015 Oct;16(5):304-11. doi: 10.2174/1389202916666150707155610.
7
The biology and function of exosomes in cancer.外泌体在癌症中的生物学特性与功能
J Clin Invest. 2016 Apr 1;126(4):1208-15. doi: 10.1172/JCI81135.
8
Versatile roles of extracellular vesicles in cancer.细胞外囊泡在癌症中的多种作用。
J Clin Invest. 2016 Apr 1;126(4):1163-72. doi: 10.1172/JCI81130. Epub 2016 Mar 14.
9
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.
10
Initial evidence that blood-borne microvesicles are biomarkers for recurrence and survival in newly diagnosed glioblastoma patients.初步证据表明,血源微泡是新诊断的胶质母细胞瘤患者复发和生存的生物标志物。
J Neurooncol. 2016 Apr;127(2):391-400. doi: 10.1007/s11060-015-2051-3. Epub 2016 Jan 8.

循环微RNA作为胶质瘤新兴的非侵入性生物标志物

Circulating microRNAs as emerging non-invasive biomarkers for gliomas.

作者信息

Santangelo Alessandra, Tamanini Anna, Cabrini Giulio, Dechecchi Maria Cristina

机构信息

Laboratory of Molecular Pathology, Department of Pathology and Diagnostics, University Hospital of Verona, Verona, Italy.

出版信息

Ann Transl Med. 2017 Jul;5(13):277. doi: 10.21037/atm.2017.06.15.

DOI:10.21037/atm.2017.06.15
PMID:28758103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5515812/
Abstract

No single circulating biomarker has been put to practice for malignant gliomas so far, the most lethal primary brain tumors. Many promising protein biomarkers such as the mutant EGFRvIII or glial fibrillary acidic protein (GFAP) have already been detected in the blood and cerebrospinal fluid (CSF) of patients with gliomas, but their clinical value is still pending validation. Furthermore, these and other proteins seem to lack sufficient sensitivity and specificity required for a successful biomarker in this clinical setting. The expression profiling of microRNAs (miRNAs) has already entered cancer clinics as diagnostic and prognostic biomarkers, for assessing tumor initiation, progression and response to treatment. Large-scale miRNA expression analyses reported both up-regulation and down-regulation of several miRNAs in tumour tissues from patients with gliomas compared to normal brain tissue, thus supporting the development of miRNA-based biomarkers. Using comprehensive high-throughput approaches, such as microarrays, different circulating miRNAs were proposed as potential biomarkers of gliomas. This review is aimed to summarize the clinical evidence about circulating miRNA biomarkers discovered to date. Mandatory issues to develop clinically validated biomarkers to improve time of diagnosis, predicting response to treatment and prognosis of patients with gliomas are also herein addresses.

摘要

迄今为止,尚无单一循环生物标志物应用于恶性胶质瘤(最致命的原发性脑肿瘤)的临床实践。许多有前景的蛋白质生物标志物,如突变型表皮生长因子受体变体Ⅲ(EGFRvIII)或胶质纤维酸性蛋白(GFAP),已在胶质瘤患者的血液和脑脊液(CSF)中被检测到,但其临床价值仍有待验证。此外,这些蛋白质以及其他蛋白质似乎缺乏在这种临床环境中成为成功生物标志物所需的足够敏感性和特异性。微小RNA(miRNA)的表达谱分析已作为诊断和预后生物标志物进入癌症临床领域,用于评估肿瘤的发生、进展及对治疗的反应。大规模miRNA表达分析报告称,与正常脑组织相比,胶质瘤患者肿瘤组织中几种miRNA既有上调也有下调,从而支持了基于miRNA的生物标志物的开发。通过使用综合高通量方法,如微阵列,不同的循环miRNA被提议作为胶质瘤的潜在生物标志物。本综述旨在总结迄今为止发现的循环miRNA生物标志物的临床证据。本文还讨论了开发经过临床验证的生物标志物以改善胶质瘤患者诊断时间、预测治疗反应和预后的关键问题。