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基于高通量纳米辅助激光解吸电离质谱的血清多组学准确鉴别良性胆道疾病和胆管癌。

Accurate Discrimination of Benign Biliary Diseases and Cholangiocarcinoma with Serum Multiomics Revealed by High-Throughput Nanoassisted Laser Desorption Ionization Mass Spectrometry.

机构信息

Lab of Nanomedicine and Omic-based Diagnostics, Institute of Analytical Chemistry, Department of Chemistry, Zhejiang University, Hangzhou 310058, China.

Department of hepatobiliary and pancreatic Surgery, First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310003, China.

出版信息

J Proteome Res. 2023 Jun 2;22(6):1855-1867. doi: 10.1021/acs.jproteome.2c00846. Epub 2023 May 23.

Abstract

Cholangiocarcinoma (CCA) is an aggressive malignant tumor with a poor prognosis. Carbohydrate antigen 19-9 is an essential biomarker for CCA diagnosis, but its low sensitivity (72%) makes the diagnosis unreliable. To explore potential biomarkers for the diagnosis of CCA, a high-throughput nanoassisted laser desorption ionization mass spectrometry technique was constructed. We performed serum lipidomics and peptidomics analyses from 112 patients with CCA and 123 patients with benign biliary diseases. Lipidomics analysis showed that various lipids, such as glycerophospholipids, glycerides, and sphingolipids, were perturbed. Peptidomics analysis revealed perturbations of multiple proteins involved in the coagulation cascade, lipid transport, and so on. After data mining, 25 characteristic molecules including 20 lipids and 5 peptides were identified as potential diagnostic biomarkers. After screening various machine learning algorithms, artificial neural network was selected to construct a multiomics model for CCA diagnosis with 96.5% sensitivity and 96.4% specificity. The sensitivity and specificity of the model in the independent test cohort were 93.8 and 87.5%, respectively. Furthermore, integrated analysis with transcriptomic data in the cancer genome atlas confirmed that genes altered in CCA significantly affected multiple lipid- and protein-related pathways. Data are available via MetaboLights with the identifier MTBLS6712.

摘要

胆管癌(CCA)是一种预后不良的侵袭性恶性肿瘤。癌抗原 19-9 是 CCA 诊断的重要生物标志物,但敏感性低(72%)导致诊断不可靠。为了探索 CCA 诊断的潜在生物标志物,构建了高通量纳米辅助激光解吸电离质谱技术。我们对 112 例 CCA 患者和 123 例良性胆道疾病患者的血清脂质组学和肽组学进行了分析。脂质组学分析表明,各种脂质如甘油磷脂、甘油三酯和鞘脂等都受到了干扰。肽组学分析显示,涉及凝血级联、脂质转运等多种蛋白质的表达发生了变化。经过数据挖掘,确定了 25 种特征分子,包括 20 种脂质和 5 种肽,作为潜在的诊断生物标志物。经过筛选各种机器学习算法,选择人工神经网络构建 CCA 诊断的多组学模型,具有 96.5%的敏感性和 96.4%的特异性。该模型在独立测试队列中的敏感性和特异性分别为 93.8%和 87.5%。此外,与癌症基因组图谱中的转录组数据的综合分析证实,CCA 中改变的基因显著影响了多个与脂质和蛋白质相关的通路。数据可通过代谢组学数据知识库(MTBLS6712)获取。

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