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Recent advances in mass spectrometry based clinical proteomics: applications to cancer research

机译:基于质谱的临床蛋白质组学的最新进展:癌症研究的应用

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Cancer biomarkers have transformed current practices in the oncology clinic. Continued discovery and validation are crucial for improving early diagnosis, risk stratification, and monitoring patient response to treatment. Profiling of the tumour genome and transcriptome are now established tools for the discovery of novel biomarkers, but alterations in proteome expression are more likely to reflect changes in tumour pathophysiology. In the past, clinical diagnostics have strongly relied on antibody-based detection strategies, but these methods carry certain limitations. Mass spectrometry (MS) is a powerful method that enables increasingly comprehensive insights into changes of the proteome to advance personalized medicine. In this review, recent improvements in MS-based clinical proteomics are highlighted with a focus on oncology. We will provide a detailed overview of clinically relevant samples types, as well as, consideration for sample preparation methods, protein quantitation strategies, MS configurations, and data analysis pipelines currently available to researchers. Critical consideration of each step is necessary to address the pressing clinical questions that advance cancer patient diagnosis and prognosis. While the majority of studies focus on the discovery of clinically-relevant biomarkers, there is a growing demand for rigorous biomarker validation. These studies focus on high-throughput targeted MS assays and multi-centre studies with standardized protocols. Additionally, improvements in MS sensitivity are opening the door to new classes of tumour-specific proteoforms including post-translational modifications and variants originating from genomic aberrations. Overlaying proteomic data to complement genomic and transcriptomic datasets forges the growing field of proteogenomics, which shows great potential to improve our understanding of cancer biology. Overall, these advancements not only solidify MS-based clinical proteomics’ integral position in cancer research, but also accelerate the shift towards becoming a regular component of routine analysis and clinical practice.
机译:癌症生物标志物在肿瘤学诊所转化了当前的实践。持续的发现和验证对于改善早期诊断,风险分层和监测对治疗的患者的反应至关重要。现在建立了肿瘤基因组和转录组的谱分析,用于发现新型生物标志物的工具,但蛋白质组表达的改变更可能反映肿瘤病理生理学的变化。过去,临床诊断强烈依赖于基于抗体的检测策略,但这些方法携带一定的限制。质谱(MS)是一种强大的方法,可以实现越来越全面的洞察蛋白质组的变化,以推进个性化药物。在本综述中,近期基于MS的临床蛋白质组学的改进是以肿瘤的重点突出显示的。我们将详细概述临床相关的样本类型,以及考虑研究人员目前可用的样品制备方法,蛋白质定量策略,MS配置和数据分析管道。对每个步骤的批判考虑是为了解决提高癌症患者诊断和预后的按压临床问题所必需的。虽然大多数研究专注于发现临床相关的生物标志物,但对严格的生物标志物验证的需求不断增长。这些研究专注于高通量靶向MS测定和具有标准化方案的多中心研究。另外,MS灵敏度的改进是向新类别的肿瘤特异性蛋白质形式的门打开门,包括翻译后修饰和源自基因组像差的变体。将蛋白质组学数据覆盖为补体基因组和转录组族数据集造成蛋白质组织的不断增长的植物领域,这表现出改善我们对癌症生物学了解的巨大潜力。总体而言,这些进步不仅巩固了基于MS的临床蛋白质组学的癌症研究中的整体位置,而且还加速了转变成为常规分析和临床实践的常规组成部分。

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