弥漫性胶质瘤的分子格局及生物标志物的发展前景。

Expert opinion on medical diagnostics Pub Date : 2013-11-01 Epub Date: 2013-10-28 DOI:10.1517/17530059.2013.846321
Jason T Huse, Kenneth D Aldape
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引用次数: 9

摘要

导读:高通量分子图谱正在改变弥漫胶质瘤这一最常见的原发性脑肿瘤长期存在的概念。事实上,全面的基因组学、转录组学和表观基因组学分析不仅为弥漫性胶质瘤的发病机制提供了惊人的见解,而且极大地丰富了潜在的生物标志物库,用于预后和预测患者分层。涵盖领域:本文总结了弥漫性胶质瘤分子表征的最新进展,重点介绍了生物标志物开发和应用的意义。在此过程中,我们还将讨论相关的高通量分子分析技术,以及将其广泛纳入疾病管理工作流程所隐含的机遇和挑战。专家意见:尽管目前指导弥漫性胶质瘤治疗的有效生物标志物数量相当少,但快速发展的分子注释继续提供稳定的临床相关候选物流,其中许多在特定靶向治疗的背景下显示出预测能力。这种潜力现在需要在精心设计的临床试验中进行严格的验证,并由标准临床材料进行强大的分子分析分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The molecular landscape of diffuse glioma and prospects for biomarker development.

Introduction: High-throughput molecular profiling is transforming long-standing conceptions of diffuse gliomas, the most common primary brain tumors. Indeed, comprehensive genomic, transcriptomic and epigenomic analyses have not only provided striking mechanistic insights into the pathogenesis of diffuse gliomas but also greatly enriched the pool of potential biomarkers for prognostic and predictive patient stratification.

Areas covered: This article summarizes significant recent developments in the molecular characterization of diffuse gliomas, focusing on implications for biomarker development and application. In doing so, we will also address relevant high-throughput molecular profiling technologies and both the opportunities and challenges implicit in their widespread incorporation into disease management workflows.

Expert opinion: Although the number of validated biomarkers guiding diffuse glioma management is currently quite small, rapidly progressing molecular annotation continues to provide a steady stream of clinically relevant candidates, many of which show promise for predictive capabilities in the context of specific targeted therapeutics. Such potential now requires rigorous validation in well-designed clinical trials supported by robust molecular profiling assays operative from standard clinical material.

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