Deborah Wenk, Charlotte Zuo, Thomas Kislinger, Lusia Sepiashvili
{"title":"Recent developments in mass-spectrometry-based targeted proteomics of clinical cancer biomarkers.","authors":"Deborah Wenk, Charlotte Zuo, Thomas Kislinger, Lusia Sepiashvili","doi":"10.1186/s12014-024-09452-1","DOIUrl":null,"url":null,"abstract":"<p><p>Routine measurement of cancer biomarkers is performed for early detection, risk classification, and treatment monitoring, among other applications, and has substantially contributed to better clinical outcomes for patients. However, there remains an unmet need for clinically validated assays of cancer protein biomarkers. Protein tumor markers are of particular interest since proteins carry out the majority of biological processes and thus dynamically reflect changes in cancer pathophysiology. Mass spectrometry-based targeted proteomics is a powerful tool for absolute peptide and protein quantification in biological matrices with numerous advantages that make it attractive for clinical applications in oncology. The use of liquid chromatography-tandem mass spectrometry (LC-MS/MS) based methodologies has allowed laboratories to overcome challenges associated with immunoassays that are more widely used for tumor marker measurements. Yet, clinical implementation of targeted proteomics methodologies has so far been limited to a few cancer markers. This is due to numerous challenges associated with paucity of robust validation studies of new biomarkers and the labor-intensive and operationally complex nature of LC-MS/MS workflows. The purpose of this review is to provide an overview of targeted proteomics applications in cancer, workflows used in targeted proteomics, and requirements for clinical validation and implementation of targeted proteomics assays. We will also discuss advantages and challenges of targeted MS-based proteomics assays for clinical cancer biomarker analysis and highlight some recent developments that will positively contribute to the implementation of this technique into clinical laboratories.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10826105/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12014-024-09452-1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
Routine measurement of cancer biomarkers is performed for early detection, risk classification, and treatment monitoring, among other applications, and has substantially contributed to better clinical outcomes for patients. However, there remains an unmet need for clinically validated assays of cancer protein biomarkers. Protein tumor markers are of particular interest since proteins carry out the majority of biological processes and thus dynamically reflect changes in cancer pathophysiology. Mass spectrometry-based targeted proteomics is a powerful tool for absolute peptide and protein quantification in biological matrices with numerous advantages that make it attractive for clinical applications in oncology. The use of liquid chromatography-tandem mass spectrometry (LC-MS/MS) based methodologies has allowed laboratories to overcome challenges associated with immunoassays that are more widely used for tumor marker measurements. Yet, clinical implementation of targeted proteomics methodologies has so far been limited to a few cancer markers. This is due to numerous challenges associated with paucity of robust validation studies of new biomarkers and the labor-intensive and operationally complex nature of LC-MS/MS workflows. The purpose of this review is to provide an overview of targeted proteomics applications in cancer, workflows used in targeted proteomics, and requirements for clinical validation and implementation of targeted proteomics assays. We will also discuss advantages and challenges of targeted MS-based proteomics assays for clinical cancer biomarker analysis and highlight some recent developments that will positively contribute to the implementation of this technique into clinical laboratories.
对癌症生物标志物进行常规测量,主要用于早期检测、风险分类和治疗监测等,大大提高了患者的临床疗效。然而,对于经过临床验证的癌症蛋白质生物标志物检测方法的需求仍未得到满足。蛋白质肿瘤标志物尤其令人感兴趣,因为蛋白质执行着大多数生物过程,因此能动态反映癌症病理生理学的变化。基于质谱的靶向蛋白质组学是对生物基质中的肽和蛋白质进行绝对定量的强大工具,它具有众多优势,因此在肿瘤学的临床应用中极具吸引力。基于液相色谱-串联质谱(LC-MS/MS)的方法使实验室能够克服与免疫测定相关的挑战,而免疫测定在肿瘤标志物测量中应用更为广泛。然而,迄今为止,靶向蛋白质组学方法的临床应用还仅限于少数几种癌症标志物。这是由于缺乏对新生物标记物的可靠验证研究以及 LC-MS/MS 工作流程的劳动密集型和操作复杂性所带来的诸多挑战。本综述旨在概述靶向蛋白质组学在癌症中的应用、靶向蛋白质组学中使用的工作流程以及靶向蛋白质组学测定的临床验证和实施要求。我们还将讨论基于 MS 的靶向蛋白质组学测定在临床癌症生物标记物分析中的优势和挑战,并重点介绍一些最新进展,这些进展将对临床实验室实施这项技术起到积极的推动作用。