Summary of Study ST003989

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR002474. The data can be accessed directly via it's Project DOI: 10.21228/M8V84X This work is supported by NIH grant, U2C- DK119886.

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This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST003989
Study TitlePlasma Amino Acids Analysis in Thai EGFR-mutated Non-Small Cell Lung Cancer Patients
Study SummaryLung cancer remains the leading cause of cancer-related deaths worldwide, emphasizing an urgent need for effective, non-invasive diagnostic and prognostic biomarkers. Metabolic reprogramming driven by oncogenic driver alterations, especially EGFR mutations in non-small cell lung cancer (NSCLC), provides promising metabolic signatures detectable in plasma. This study aimed to identify plasma metabolomic biomarkers distinguishing healthy individuals from NSCLC patients and to further stratify NSCLC patients by EGFR mutation status and EGFR tyrosine kinase inhibitor (TKI) resistance. Using gas chromatography-mass spectrometry (GC-MS), we quantified 21 amino acids of 78 individuals, including NSCLC patients and healthy controls.
Institute
Mahidol University
Last NameKhoomrung
First NameSakda
Address2 Wanglang road, Bangkoknoi, Bangkok 10700. Thailand.
Emailsiriphan.man@mahidol.edu
Phone025195505
Submit Date2025-06-02
Raw Data AvailableYes
Raw Data File Type(s)mzML, d
Analysis Type DetailGC-MS
Release Date2025-07-07
Release Version1
Sakda Khoomrung Sakda Khoomrung
https://dx.doi.org/10.21228/M8V84X
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR002474
Project DOI:doi: 10.21228/M8V84X
Project Title:Plasma Metabolomic Analysis in Thai EGFR-mutated Non-Small Cell Lung Cancer Patients
Project Summary:Lung cancer remains the leading cause of cancer-related deaths worldwide, emphasizing an urgent need for effective, non-invasive diagnostic and prognostic biomarkers. Metabolic reprogramming driven by oncogenic driver alterations, especially EGFR mutations in non-small cell lung cancer (NSCLC), provides promising metabolic signatures detectable in plasma. This study aimed to identify plasma metabolomic biomarkers distinguishing healthy individuals from NSCLC patients and to further stratify NSCLC patients by EGFR mutation status and EGFR tyrosine kinase inhibitor (TKI) resistance. Using gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS/MS), we quantified four groups of targeted metabolites (amino acids, organic acids, sugar and sugar alcohols, and phospholipids) of 78 individuals, including NSCLC patients and healthy controls. Metabolomic signatures distinctly separated healthy controls from NSCLC patients and, furthermore, EGFR-mutated NSCLC from EGFR wild-type cases. Additionally, metabolomics results effectively distinguished EGFR TKI-resistant from treatment-naïve EGFR-mutated NSCLC. Our findings highlight the potential of plasma metabolites as minimally invasive biomarkers for molecular classification and monitoring therapeutic response in NSCLC patients.
Institute:Mahidol University
Last Name:Khoomrung
First Name:Sakda
Address:2 Wanglang road, Bangkoknoi, Bangkok 10700. Thailand.
Email:Sakda.kho@mahidol.edu
Phone:024195505

Subject:

Subject ID:SU004126
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606
Gender:Male and female

Factors:

Subject type: Human; Subject species: Homo sapiens (Factor headings shown in green)

mb_sample_id local_sample_id Sample source Disease EGFR mutation Treatment
SA454850C05Plasma Healthy n/a n/a
SA454851C01Plasma Healthy n/a n/a
SA454852C03Plasma Healthy n/a n/a
SA454853C04Plasma Healthy n/a n/a
SA454854C02Plasma Healthy n/a n/a
SA454855C06Plasma Healthy n/a n/a
SA454856C07Plasma Healthy n/a n/a
SA454857C08Plasma Healthy n/a n/a
SA454858C09Plasma Healthy n/a n/a
SA454859C10Plasma Healthy n/a n/a
SA454860B22Plasma NSCLC No Naïve
SA454861B11Plasma NSCLC No Naïve
SA454862B12Plasma NSCLC No Naïve
SA454863B14Plasma NSCLC No Naïve
SA454864B15Plasma NSCLC No Naïve
SA454865B16Plasma NSCLC No Naïve
SA454866B17Plasma NSCLC No Naïve
SA454867B18Plasma NSCLC No Naïve
SA454868B19Plasma NSCLC No Naïve
SA454869B21Plasma NSCLC No Naïve
SA454870B28Plasma NSCLC No Naïve
SA454871B23Plasma NSCLC No Naïve
SA454872B24Plasma NSCLC No Naïve
SA454873B25Plasma NSCLC No Naïve
SA454874B26Plasma NSCLC No Naïve
SA454875B27Plasma NSCLC No Naïve
SA454876B09Plasma NSCLC No Naïve
SA454877B30Plasma NSCLC No Naïve
SA454878B33Plasma NSCLC No Naïve
SA454879B34Plasma NSCLC No Naïve
SA454880B42Plasma NSCLC No Naïve
SA454881B10Plasma NSCLC No Naïve
SA454882B13Plasma NSCLC No Naïve
SA454883B08Plasma NSCLC No Naïve
SA454884B06Plasma NSCLC No Naïve
SA454885B05Plasma NSCLC No Naïve
SA454886B02Plasma NSCLC No Naïve
SA454887B07Plasma NSCLC No Naïve
SA454888B01Plasma NSCLC No Naïve
SA454889A25Plasma NSCLC Yes Naïve
SA454890A29Plasma NSCLC Yes Naïve
SA454891A28Plasma NSCLC Yes Naïve
SA454892A27Plasma NSCLC Yes Naïve
SA454893A26Plasma NSCLC Yes Naïve
SA454894A22Plasma NSCLC Yes Naïve
SA454895A24Plasma NSCLC Yes Naïve
SA454896A23Plasma NSCLC Yes Naïve
SA454897A32Plasma NSCLC Yes Naïve
SA454898A20Plasma NSCLC Yes Naïve
SA454899A14Plasma NSCLC Yes Naïve
SA454900A13Plasma NSCLC Yes Naïve
SA454901A31Plasma NSCLC Yes Naïve
SA454902A30Plasma NSCLC Yes Naïve
SA454903A33Plasma NSCLC Yes Naïve
SA454904A41Plasma NSCLC Yes Naïve
SA454905A02Plasma NSCLC Yes Naïve
SA454906A34Plasma NSCLC Yes Naïve
SA454907A45Plasma NSCLC Yes Naïve
SA454908A43Plasma NSCLC Yes Naïve
SA454909A42Plasma NSCLC Yes Naïve
SA454910A46Plasma NSCLC Yes Naïve
SA454911A40Plasma NSCLC Yes Naïve
SA454912A35Plasma NSCLC Yes Naïve
SA454913A39Plasma NSCLC Yes Naïve
SA454914A01Plasma NSCLC Yes Naïve
SA454915A36Plasma NSCLC Yes Naïve
SA454916A37Plasma NSCLC Yes Naïve
SA454917A38Plasma NSCLC Yes Naïve
SA454918D01Plasma NSCLC Yes TKI resistant
SA454919D02Plasma NSCLC Yes TKI resistant
SA454920D04Plasma NSCLC Yes TKI resistant
SA454921D05Plasma NSCLC Yes TKI resistant
SA454922D06Plasma NSCLC Yes TKI resistant
SA454923D08Plasma NSCLC Yes TKI resistant
SA454924D09Plasma NSCLC Yes TKI resistant
SA454925D10Plasma NSCLC Yes TKI resistant
SA454926D11Plasma NSCLC Yes TKI resistant
SA454927D03Plasma NSCLC Yes TKI resistant
Showing results 1 to 78 of 78

Collection:

Collection ID:CO004119
Collection Summary:Blood was drawn directly into Cell-Free DNA BCT® tubes to stabilize cell-free DNA. Plasma was separated from cellular components by centrifugation. For NSCLC patients, plasma was first subjected to EGFR mutation analysis. Plasma aliquots from all participants were stored at −80°C until subsequent analysis.
Sample Type:Blood (plasma)

Treatment:

Treatment ID:TR004135
Treatment Summary:Treatment-naïve NSCLC patients had never received any systemic treatment for lung cancer. EGFR TKI-resistant NSCLC patients had evidence of disease progression according to the Response Evaluation Criteria In Solid Tumors (RECIST) version 1.1 after receiving first- or second-generation EGFR TKI treatment. All EGFR TKI-resistant NSCLC patients had acquired EGFR T790M mutation.

Sample Preparation:

Sampleprep ID:SP004132
Sampleprep Summary:For free amino acids, plasma samples (50 µL) were vortexed with 4 mL of 25% acetonitrile in 0.1 M HCl for 2 min and sonicated at room temperature for 20 min., centrifuged at 9000 x g for 10 min. An aliquot (50 µL) of the supernatant was transferred to a 2 mL GC glass vial, which was added with 50 µL of norleucine (200 nmol/mL) as an internal standard. Then, the mixture was dried at 60°C about 1-2 hr, added with 50 µL dichloromethane, and dried again for 30 min. The dried samples were added with 50 µL of derivatizing agent, N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide with 1% tert-Butyldimethylchlorosilane (MTBSTFA + 1% TBDMSCl) and 50 µL of acetonitrile. The samples were sealed with an aluminum cap with PTFE/Red Rubber Septa and incubated at 100°C for 4 hr in a hot-air oven. After the sample was left at room temperature, 2 µL of the sample was analyzed by GC-MS/MS.

Chromatography:

Chromatography ID:CH004987
Chromatography Summary:The chromatographic analysis was performed on a gas chromatography (Agilent; 7890B) equipped with a mass spectrometer (Agilent, 7000D) and PAL auto sampler system. A 2 µL of sample was injected to GC-MS with split mode at a 1:5 split ratio at 280°C into a DB-5MS column (30 m, 0.25 mm id). Helium was used as a carrier gas with a constant flow rate of 1.4 mL/min. The GC oven was programmed as follows: ramp from 130°C to 190°C (6°C/min) and to 230°C (30°C/min), held at 230°C for 5 min, then ramp to 325 °C, and held at 325°C for 6 min. The transfer line, ion source, and quadrupole were set as 325°C, 240°C, and 180 °C, respectively.
Instrument Name:Agilent 6890N
Column Name:Agilent DB5-MS (30 m x 0.25 mm, 0.25 µm)
Column Temperature:not applicable
Flow Gradient:not applicable
Flow Rate:1.4 mL/min
Solvent A:not applicable
Solvent B:not applicable
Chromatography Type:GC

Analysis:

Analysis ID:AN006570
Analysis Type:MS
Chromatography ID:CH004987
Num Factors:4
Num Metabolites:21
Units:micro molar
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