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A pilot study identifying a potential plasma biomarker for determining EGFR mutations in exons 19 or 21 in lung cancer patients

Authors
Pamungkas, Aryo D.Medriano, Carl A.Sim, EunjungLee, SungyongPark, Youngja H.
Issue Date
6월-2017
Publisher
SPANDIDOS PUBL LTD
Keywords
lung cancer; liquid chromatography-mass spectrometry; high-resolution metabolomics; epidermal growth factor receptor mutation; biomarker
Citation
MOLECULAR MEDICINE REPORTS, v.15, no.6, pp.4155 - 4161
Indexed
SCIE
SCOPUS
Journal Title
MOLECULAR MEDICINE REPORTS
Volume
15
Number
6
Start Page
4155
End Page
4161
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/83314
DOI
10.3892/mmr.2017.6530
ISSN
1791-2997
Abstract
The most common type of lung cancer is non-small cell lung cancer (NSCLC), which is frequently characterized by a mutation in the epidermal growth factor receptor (EGFR). Determining the presence of an EGFR mutation in lung cancer is important, as it determines the type of treatment that a patients will receive. Therefore, the aim of the present study was to apply high-resolution metabolomics (HRM) using liquid chromatography-mass spectrometry to identify significant compounds in human plasma samples obtained from South Korean NSCLC patients, as potential biomarkers for providing early detection and diagnosis of minimally-invasive NSCLC. The metabolic differences between lung cancer patients without EGFR mutations were compared with patients harboring EGFR mutations. Univariate analysis was performed, with a false discovery rate of q=0.05, in order to identify significant metabolites between the two groups. In addition, hierarchical clustering analysis was performed to discriminate between the metabolic profiles of the two groups. Furthermore, the significant metabolites were identified and mapped using Mummichog software, in order to generate a potential metabolic network model. Using metabolome-wide association studies, metabolic alterations were identified. Linoleic acid [303.23 m/z, (M+Na)+], 5-methyl tetrahydrofolate [231.10 m/z, (M+2H)+] and N-succinyl-L-glutamate-5 semialdehyde [254.06 m/z, (M+Na)+], were observed to be elevated in patients harboring EGFR mutations, whereas tetradecanoyl carnitine [394.29 m/z, (M+Na)+] was observed to be reduced. This suggests that these compounds may be affected by the EGFR mutation. In conclusion, the present study identified four potential biomarkers in patients with EGFR mutations, using HRM combined with pathway analysis. These results may facilitate the development of novel diagnostic tools for EGFR mutation detection in patients with lung cancer.
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