Roberto Gasparri, Roberta Noberini, Alessandro Cuomo, Avinash Yadav, Davide Tricarico, Carola Salvetto, Patrick Maisonneuve, Valentina Caminiti, Giulia Sedda, Angela Sabalic, Tiziana Bonaldi, Lorenzo Spaggiari
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引用次数: 0
Abstract
Purpose: Lung cancer is the most common cause of death from cancer worldwide, largely due to late diagnosis. Thus, there is an urgent need to develop new approaches to improve the detection of early-stage lung cancer, which would greatly improve patient survival.
Experimental design: The quantitative protein expression profiles of microvesicles isolated from the sera from 46 lung cancer patients and 41 high-risk non-cancer subjects were obtained using a mass spectrometry method based on a peptide library matching approach.
Results: We identified 33 differentially expressed proteins that allow discriminating the two groups. We also built a machine learning model based on serum protein expression profiles that can correctly classify the majority of lung cancer cases and that highlighted a decrease in the levels of Arysulfatase A (ARSA) as the most discriminating factor found in tumors.
Conclusions and clinical relevance: Our study identified a preliminary, non-invasive protein signature able to discriminate with high specificity and selectivity early-stage lung cancer patients from high-risk healthy subjects. These results provide the basis for future validation studies for the development of a non-invasive diagnostic tool for lung cancer.
目的:肺癌是世界范围内最常见的癌症死亡原因,主要是由于诊断较晚。因此,迫切需要开发新的方法来提高早期肺癌的检测,从而大大提高患者的生存率。实验设计:采用基于肽库匹配的质谱方法,从46例肺癌患者和41例高危非癌症患者的血清中分离得到微囊泡的定量蛋白表达谱。结果:我们鉴定了33个差异表达蛋白,可以区分两组。我们还建立了一个基于血清蛋白表达谱的机器学习模型,该模型可以正确地对大多数肺癌病例进行分类,并强调Arysulfatase a (ARSA)水平的降低是肿瘤中发现的最具区别性的因素。结论和临床意义:我们的研究确定了一种初步的、非侵入性的蛋白质特征,能够高特异性和选择性地区分早期肺癌患者和高风险的健康受试者。这些结果为未来肺癌非侵入性诊断工具的开发提供了验证研究的基础。