通过 1H 磁共振波谱检测痰液和呼出气体凝结物中肺癌的代谢特征:可行性研究。

Magnetic resonance insights Pub Date : 2016-11-17 eCollection Date: 2016-01-01 DOI:10.4137/MRI.S40864
Naseer Ahmed, Tedros Bezabeh, Omkar B Ijare, Renelle Myers, Reem Alomran, Michel Aliani, Zoann Nugent, Shantanu Banerji, Julian Kim, Gefei Qing, Zoheir Bshouty
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引用次数: 0

摘要

目标:肺癌是最致命的癌症之一:肺癌是致死率最高的癌症之一。目前,还没有用于早期检测、监测治疗反应和检测复发性肺癌的生物标记物。我们开展了这项研究,以确定痰液和呼出气体冷凝物(EBC)的 1H 磁共振波谱(MRS)作为一种非侵入性工具能否识别肺癌的代谢生物标记物:收集了 20 名患者的痰液和 EBC 样本,其中包括病理确诊的非小细胞肺癌患者(10 人)和良性呼吸道疾病患者(10 人)。18 名患者同时采集了痰和 EBC 样本;2 名患者仅提供了 EBC 样本。1H MR 图谱由布鲁克 Avance 400 MHz 核磁共振 (NMR) 光谱仪获得。对痰样本进一步进行细胞学确认,以区分真痰和唾液:在 EBC 样本中,肺癌患者丙酸盐、乙醇、乙酸盐和丙酮的中位浓度高于良性患者。肺癌患者甲醇的中位浓度(0.028 毫摩尔)低于良性患者(0.067 毫摩尔;P = 0.028)。在痰液和唾液以及经细胞学确诊的痰液样本中,肺癌患者的 N-乙酰糖、糖蛋白、丙酸盐、赖氨酸、乙酸盐和甲酸盐的中位浓度均低于良性患者。在肺癌患者的痰液和唾液联合样本(88%)以及经细胞学确诊的痰液样本(86%)中,葡萄糖始终不存在:结论:通过 1H MRS 发现的肺癌患者痰液中不含葡萄糖和 EBC 中甲醇浓度较低的现象可作为肺癌的代谢生物标记物,用于早期发现、监测治疗反应和检测复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolic Signatures of Lung Cancer in Sputum and Exhaled Breath Condensate Detected by 1H Magnetic Resonance Spectroscopy: A Feasibility Study.

Objectives: Lung cancer is one of the most lethal cancers. Currently, there are no biomarkers for early detection, monitoring treatment response, and detecting recurrent lung cancer. We undertook this study to determine if 1H magnetic resonance spectroscopy (MRS) of sputum and exhaled breath condensate (EBC), as a noninvasive tool, can identify metabolic biomarkers of lung cancer.

Materials and methods: Sputum and EBC samples were collected from 20 patients, comprising patients with pathologically confirmed non-small cell lung cancer (n = 10) and patients with benign respiratory conditions (n = 10). Both sputum and EBC samples were collected from 18 patients; 2 patients provided EBC samples only. 1H MR spectra were obtained on a Bruker Avance 400 MHz nuclear magnetic resonance (NMR) spectrometer. Sputum samples were further confirmed cytologically to distinguish between true sputum and saliva.

Results: In the EBC samples, median concentrations of propionate, ethanol, acetate, and acetone were higher in lung cancer patients compared to the patients with benign conditions. Median concentration of methanol was lower in lung cancer patients (0.028 mM) than in patients with benign conditions (0.067 mM; P = 0.028). In the combined sputum and saliva and the cytologically confirmed sputum samples, median concentrations of N-acetyl sugars, glycoprotein, propionate, lysine, acetate, and formate were lower in the lung cancer patients than in patients with benign conditions. Glucose was found to be consistently absent in the combined sputum and saliva samples (88%) as well as in the cytologically confirmed sputum samples (86%) of lung cancer patients.

Conclusion: Absence of glucose in sputum and lower concentrations of methanol in EBC of lung cancer patients discerned by 1H MRS may serve as metabolic biomarkers of lung cancer for early detection, monitoring treatment response, and detecting recurrence.

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