Exhaled metabolic markers and relevant dysregulated pathways of lung cancer: a pilot study

被引:14
作者
Zou, Yingchang [1 ,2 ]
Hu, Yanjie [3 ]
Jiang, Zaile [4 ]
Chen, Ying [1 ]
Zhou, Yuan [1 ]
Wang, Zhiyou [1 ,2 ]
Wang, Yu [5 ]
Jiang, Guobao [1 ]
Tan, Zhiguang [1 ]
Hu, Fangrong [1 ,2 ]
机构
[1] Changsha Univ, Sch Elect Informat & Elect Engn, Changsha, Peoples R China
[2] Hunan Engn Technol Res Ctr Optoelect Hlth Detect, Changsha, Peoples R China
[3] Zhejiang Univ, Zhejiang Sir Run Run Shaw Hosp, Dept Med, Hangzhou, Peoples R China
[4] Tianhe Culture Chain Technol Co Ltd, Changsha, Peoples R China
[5] Res Ctr Healthcare Data Sci, Zhijiang Lab, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Exhaled metabolic markers; volatile organic compounds; pathway enrichment; lung cancer; metabolomics; VOLATILE ORGANIC-COMPOUNDS; GENE-EXPRESSION; BIOMARKERS; SAMPLES; PLASMA; SERUM; RISK; VOCS;
D O I
10.1080/07853890.2022.2048064
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction The clinical application of lung cancer detection based on breath test is still challenging due to lack of predictive molecular markers in exhaled breath. This study explored potential lung cancer biomarkers and their related pathways using a typical process for metabolomics investigation. Material and methods Breath samples from 60 lung cancer patients and 176 healthy people were analyzed by GC-MS. The original data were GC-MS peak intensity removing background signal. Differential metabolites were selected after univariate statistical analysis and multivariate statistical analysis based on OPLS-DA and Spearman rank correlation analysis. A multivariate PLS-DA model was established based on differential metabolites for pattern recognition. Subsequently, pathway enrichment analysis was performed on differential metabolites. Results The discriminant capability was assessed by ROC curve of whom the average AUC and average accuracy in 100-fold cross validations were 0.871 and 0.787, respectively. Eight potential biomarkers were involved in a total of 18 metabolic pathways. Among them, 11 metabolic pathways have p-value smaller than .1. Discussion Some pathways among them are related to risk factors or therapies of lung cancer. However, more of them are dysregulated pathways of lung cancer reported in studies based on genome or transcriptome data. Conclusion We believe that it opens the possibility of using metabolomics methods to analyze data of exhaled breath and promotes involvement of knowledge dataset to cover more volatile metabolites. Clinical significance Although a series of related research reported diagnostic models with highly sensitive and specific prediction, the clinical application of lung cancer detection based on breath test is still challenging due to disease heterogeneity and lack of predictive molecular markers in exhaled breath. This study may promote the clinical application of this technique which is suitable for large-scale screening thanks to its low-cost and non-invasiveness. As a result, the mortality of lung cancer may be decreased in future. Key messages In the present study, 11 pathways involving 8 potential biomarkers were discovered to be dysregulated pathways of lung cancer. We found that it is possible to apply metabolomics methods in analysis of data from breath test, which is meaningful to discover convinced volatile markers with definite pathological and histological significance.
引用
收藏
页码:790 / 802
页数:13
相关论文
共 47 条
[1]   Metabolomics profiling and pathway analysis of human plasma and urine reveal further insights into the multifactorial nature of coronary artery disease [J].
Amin, Arwa M. ;
Mostafa, Hamza ;
Arif, Nor Hayati ;
Kader, Muhamad Ali S. K. Abdul ;
Hay, Yuen Kah .
CLINICA CHIMICA ACTA, 2019, 493 :112-122
[2]   Exploring candidate biomarkers for lung and prostate cancers using gene expression and flux variability analysis [J].
Asgari, Yazdan ;
Khosravi, Pegah ;
Zabihinpour, Zahra ;
Habibi, Mahnaz .
INTEGRATIVE BIOLOGY, 2018, 10 (02) :113-120
[3]   Variations of chromosome 2 gene expressions among patients with lung cancer or non-cancer [J].
Bao, Lianmin ;
Zhang, Yong ;
Wang, Jian ;
Wang, Haiyun ;
Dong, Nian ;
Su, Xiaoqiong ;
Xu, Menglin ;
Wang, Xiangdong .
CELL BIOLOGY AND TOXICOLOGY, 2016, 32 (05) :419-435
[4]   Expiratory flow rate, breath hold and anatomic dead space influence electronic nose ability to detect lung cancer [J].
Bikov, Andras ;
Hernadi, Marton ;
Korosi, Beata Zita ;
Kunos, Laszlo ;
Zsamboki, Gabriella ;
Sutto, Zoltan ;
Tarnoki, Adam Domonkos ;
Tarnoki, David Laszlo ;
Losonczy, Gyorgy ;
Horvath, Ildiko .
BMC PULMONARY MEDICINE, 2014, 14
[5]   Lung Cancer Risk Among Smokers of Menthol Cigarettes [J].
Blot, William J. ;
Cohen, Sarah S. ;
Aldrich, Melinda ;
McLaughlin, Joseph K. ;
Hargreaves, Margaret K. ;
Signorello, Lisa B. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2011, 103 (10) :810-816
[6]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21492, 10.3322/caac.21609]
[7]   Menthol cigarettes and risk of lung cancer [J].
Brooks, DR ;
Palmer, JR ;
Strom, BL ;
Rosenberg, L .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2003, 158 (07) :609-616
[8]   Exhaled breath condensate biomarkers for lung cancer [J].
Campanella, Annalisa ;
De Summa, Simona ;
Tommasi, Stefania .
JOURNAL OF BREATH RESEARCH, 2019, 13 (04)
[9]   Varied Pathways of Stage IA Lung Adenocarcinomas Discovered by Integrated Gene Expression Analysis [J].
Chen, Chengwen ;
Fu, Xuping ;
Zhang, Deqiang ;
Li, Yuan ;
Xie, Yi ;
Li, Yao ;
Huang, Yan .
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, 2011, 7 (05) :551-566
[10]   Calculated indices of volatile organic compounds (VOCs) in exhalation for lung cancer screening and early detection [J].
Chen, Xing ;
Muhammad, Kanhar Ghulam ;
Madeeha, Channa ;
Fu, Wei ;
Xu, Linxin ;
Hu, Yanjie ;
Liu, Jun ;
Ying, Kejing ;
Chen, Liying ;
Yurievna, Gorlova Olga .
LUNG CANCER, 2021, 154 :197-205