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首页> 外文期刊>Scientific reports. >Simultaneous Quantification of Serum Nonesterified and Esterified Fatty Acids as Potential Biomarkers to Differentiate Benign Lung Diseases from Lung Cancer
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Simultaneous Quantification of Serum Nonesterified and Esterified Fatty Acids as Potential Biomarkers to Differentiate Benign Lung Diseases from Lung Cancer

机译:同时定量血清硝酸化和酯化脂肪酸作为潜在的生物标志物,以区分肺癌的良性肺病

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In this study, we have employed graphene oxide as a matrix to simultaneously and directly quantify serum nonesterified and esterified fatty acids (FAs) using matrix-assisted laser/desorption ionization-Fourier transform ion cyclotron resonance mass spectrometry (MALDI-FTICR MS). Twelve serum nonesterified FAs combined with their individual esterified FAs (i.e., C16:0, C16:1, C18:0, C18:1, C18:2, C18:3, C20:2, C20:3, C20:4, C20:5, C22:5, and C22:6) were quantified based on their calibration curves with the correlation coefficients of 0.99, along with the analytical time of 1?min each sample. As a result, serum levels of twelve total FAs (TFAs) in 1440 serum samples from 487 healthy controls (HCs), 479 patients with benign lung diseases (BLDs) and 474 patients with lung cancer (LC) were determined. Statistical analysis indicated that significantly increased levels of C16:0, C16:1, C18:0, C18:1, C18:3, C20:3, and C22:6 and decreased levels of C20:5 were observed in LC patients compared with BLDs. Receiver operating characteristic (ROC) analysis revealed that panel a (C18:2, C20:3, C20:4, C20:5, C22:5, and C22:6), panel b (C18:0, C20:4, C20:5, and C22:6), and panel c (C16:1, C18:0, C18:1, C20:3, and C22:6) have exhibited good diagnostic ability to differentiate BLDs from LC relative to clinical uses of tumor markers (CEA and Cyfra 21-1).
机译:在本研究中,我们使用石墨烯氧化物作为基质,同时使用基质辅助激光/解吸电离 - 傅里叶变换离子回旋谐振质谱(MALDI-FTICR MS)直接定量血清硝酸化和酯化脂肪酸(FAS)。 12个血清无敏化Fas与其单独的酯化Fas(即C16:0,C16:1,C18:0,C18:1,C18:2,C18:3,C20:2,C20:3,C20:4,C20 :5,C22:5和C22:6基于其校准曲线,其相关系数> 0.99的相关系数,以及每个样品的分析时间<1?分钟。结果,1440例健康对照(HCS),479例良性肺病(BLD)和474例肺癌(LC)患者的1440例血清样品中的血清血清水平(TFA)。统计学分析表明,在LC患者中,在LC患者中观察到显着增加C16:0,C16:1,C18:0,C18:1,C18:3,C20:3,C18:3,C20:3和C22:6的水平降低,C20:5的水平降低。 BLD。接收器操作特征(ROC)分析显示,面板A(C18:2,C20:3,C20:4,C20:5,C22:5和C22:6),Panel B(C18:0,C20:4,C20 :5和C22:6),和C16:1,C18:0,C18:1,C20:3和C22:6)表现出良好的诊断能力,可将来自LC的BLD分化为肿瘤的临床用途标记(CEA和CYFRA 21-1)。

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