Molecular Biomarkers Department, Merck Research Laboratories, 770 Sumneytown Pike, West Point, PA, 19486, USA.
Adv Exp Med Biol. 2014;806:341-59. doi: 10.1007/978-3-319-06068-2_16.
Advances in mass spectrometry, proteomics, protein bioanalytical approaches, and biochemistry have led to a rapid evolution and expansion in the area of mass spectrometry-based biomarker discovery and development. The last decade has also seen significant progress in establishing accepted definitions, guidelines, and criteria for the analytical validation, acceptance, and qualification of biomarkers. These advances have coincided with a decreased return on investment for pharmaceutical research and development and an increasing need for better early decision making tools. Empowering development teams with tools to measure a therapeutic interventions impact on disease state and progression, measure target engagement, and to confirm predicted pharmacodynamic effects is critical to efficient data-driven decision making. Appropriate implementation of a biomarker or a combination of biomarkers can enhance understanding of a drugs mechanism, facilitate effective translation from the preclinical to clinical space, enable early proof of concept and dose selection, and increase the efficiency of drug development. Here we will provide descriptions of the different classes of biomarkers that have utility in the drug development process as well as review specific, protein-centric, mass spectrometry-based approaches for the discovery of biomarkers and development of targeted assays to measure these markers in a selective and analytically precise manner.
质谱学、蛋白质组学、蛋白质生物分析方法和生物化学的进步推动了基于质谱的生物标志物发现和开发领域的快速发展和扩展。过去十年,在为生物标志物的分析验证、验收和鉴定建立公认的定义、准则和标准方面也取得了重大进展。这些进步与制药研发投资回报率下降以及对更好的早期决策工具的需求增加同时发生。为研发团队提供工具,以衡量治疗干预对疾病状态和进展的影响、衡量目标参与度,并确认预测的药效学效应,对于高效的数据驱动决策至关重要。适当实施生物标志物或生物标志物组合可以增强对药物机制的理解,促进从临床前到临床的有效转化,实现早期概念验证和剂量选择,并提高药物开发的效率。在这里,我们将描述在药物开发过程中具有实用价值的不同类别的生物标志物,并回顾特定的、以蛋白质为中心的、基于质谱的方法,用于发现生物标志物,并开发靶向分析,以选择性和分析上精确的方式测量这些标记物。