Psatha Konstantina, Kollipara Laxmikanth, Voutyraki Chrysanthi, Divanach Peter, Sickmann Albert, Rassidakis George Z, Drakos Elias, Aivaliotis Michalis
Institute of Molecular Biology and Biotechnology, FORTH, Heraklion, Greece; School of Medicine, National and Kapodistrian University of Athens, Athens, Greece; Department of Pathology, School of Medicine, University of Crete, Heraklion, Greece.
Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V., Dortmund, Germany.
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Mar 15;1047:2-14. doi: 10.1016/j.jchromb.2016.11.005. Epub 2016 Nov 15.
Mass spectrometry-based quantitative proteomics specifically applied to comprehend the pathogenesis of lymphoma has incremental value in deciphering the heterogeneity in complex deregulated molecular mechanisms/pathways of the lymphoma entities, implementing the current diagnostic and therapeutic strategies. Essential global, targeted and functional differential proteomics analyses although still evolving, have been successfully implemented to shed light on lymphoma pathogenesis to discover and explore the role of potential lymphoma biomarkers and drug targets. This review aims to outline and appraise the present status of MS-based quantitative proteomic approaches in lymphoma research, introducing the current state-of-the-art MS-based proteomic technologies, the opportunities they offer in biological discovery in human lymphomas and the related limitation issues arising from sample preparation to data evaluation. It is a synopsis containing information obtained from recent research articles, reviews and public proteomics repositories (PRIDE). We hope that this review article will aid, assimilate and assess all the information aiming to accelerate the development and validation of diagnostic, prognostic or therapeutic targets for an improved and empowered clinical proteomics application in lymphomas in the nearby future.
基于质谱的定量蛋白质组学专门用于理解淋巴瘤的发病机制,在解读淋巴瘤实体复杂失调的分子机制/途径中的异质性以及实施当前的诊断和治疗策略方面具有越来越大的价值。尽管基本的全局、靶向和功能差异蛋白质组学分析仍在不断发展,但已成功用于阐明淋巴瘤发病机制,以发现和探索潜在淋巴瘤生物标志物及药物靶点的作用。本综述旨在概述和评估基于质谱的定量蛋白质组学方法在淋巴瘤研究中的现状,介绍当前基于质谱的蛋白质组学技术的最新进展、它们在人类淋巴瘤生物学发现中提供的机会以及从样品制备到数据评估所产生的相关局限性问题。这是一篇包含从近期研究文章、综述和公共蛋白质组学知识库(PRIDE)中获取信息的概要。我们希望这篇综述文章将有助于整理、吸收和评估所有信息,旨在加速诊断、预后或治疗靶点的开发和验证,以便在不久的将来在淋巴瘤中实现改进和有力的临床蛋白质组学应用。