Santangelo Alessandra, Tamanini Anna, Cabrini Giulio, Dechecchi Maria Cristina
Laboratory of Molecular Pathology, Department of Pathology and Diagnostics, University Hospital of Verona, Verona, Italy.
Ann Transl Med. 2017 Jul;5(13):277. doi: 10.21037/atm.2017.06.15.
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.
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。