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基于 DIGE 的血液癌症生物标志物发现。

DIGE-Based Biomarker Discovery in Blood Cancers.

机构信息

Department of Biology, Maynooth University, National University of Ireland, Maynooth, Co. Kildare, Ireland.

出版信息

Methods Mol Biol. 2023;2596:105-112. doi: 10.1007/978-1-0716-2831-7_8.

Abstract

Cancer of blood or bone marrow-derived cells dysregulates normal hematopoiesis and accounts for over 6% of all cancer cases annually. Proteomic analyses of blood cancers have improved our understanding of disease mechanisms and identified numerous proteins of clinical relevance. For many years, gel-based proteomic studies have aided in the discovery of novel diagnostic, prognostic, and predictive biomarkers, as well as therapeutic targets, in various diseases, including blood cancer. Fluorescence two-dimensional difference gel electrophoresis (2D-DIGE) facilitates comparative proteomic research to identify differential protein expression in a simple and reproducible manner. The versatility of 2D-DIGE as a quantitative proteomic technique has provided insight into various aspects of blood cancer pathology, including disease development, prognostic subtypes, and drug resistance. The ability to couple 2D-DIGE with additional downstream mass spectrometry-based techniques yields comprehensive workflows capable of identifying proteins of biological and clinical significance. The application of 2D-DIGE in blood cancer research has significantly contributed to the increasingly important initiative of precision medicine. This chapter will focus on the influential role of 2D-DIGE as a tool in blood cancer research.

摘要

血液或骨髓来源的细胞癌症会扰乱正常的造血功能,每年占所有癌症病例的 6%以上。血液癌症的蛋白质组学分析提高了我们对疾病机制的理解,并确定了许多具有临床相关性的蛋白质。多年来,基于凝胶的蛋白质组学研究有助于发现各种疾病(包括血液癌症)中的新的诊断、预后和预测生物标志物以及治疗靶点。荧光二维差异凝胶电泳(2D-DIGE)以简单且可重复的方式促进比较蛋白质组学研究,以识别差异蛋白表达。2D-DIGE 作为一种定量蛋白质组学技术的多功能性为血液癌症病理学的各个方面提供了深入的了解,包括疾病发展、预后亚型和耐药性。将 2D-DIGE 与其他基于质谱的下游技术相结合的能力产生了能够识别具有生物学和临床意义的蛋白质的综合工作流程。2D-DIGE 在血液癌症研究中的应用极大地促进了精准医学这一日益重要的计划。本章将重点介绍 2D-DIGE 作为血液癌症研究工具的重要作用。

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