Abstract | BACKGROUND: METHODS: A total of 46 ESCC patients were included in this study. Gas chromatography time-of- flight mass spectrometry (GC-TOF/MS) technology was applied to detect the plasma samples collected before nCRT via untargeted metabolomics analysis. RESULTS: Five differentially expressed metabolites (out of 109) was found in plasma between pCR and non-pCR groups. Compared with non-pCR group, isocitric acid (p = 0.0129), linoleic acid (p = 0.0137), citric acid (p = 0.0473) were upregulated, while L-histidine (p = 0.0155), 3'4 dihydroxyhydrocinnamic acid (p = 0.0339) were downregulated in the pCR plasma samples. Pathway analyses unveiled that citrate cycle (TCA cycle), glyoxylate and dicarboxylate metabolic pathway were associated with ESCC chemoradiosensitivity. CONCLUSION: The present study provided supporting evidence that GC-TOF/MS based metabolomics approach allowed identification of metabolite differences between pCR and non-pCR patients in plasma levels, and the systemic metabolic status of patients may reflect the response of ESCC patient to neoadjuvant chemoradiotherapy.
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Authors | Yaowen Zhang, Jianpo Wang, Ningtao Dai, Peng Han, Jian Li, Jiangman Zhao, Weilan Yuan, Jiahuan Zhou, Fuyou Zhou |
Journal | BMC cancer
(BMC Cancer)
Vol. 20
Issue 1
Pg. 835
(Sep 02 2020)
ISSN: 1471-2407 [Electronic] England |
PMID | 32878621
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Aged
- Aged, 80 and over
- Biomarkers, Tumor
(blood)
- Chemoradiotherapy
(methods)
- Esophageal Neoplasms
(blood, pathology, therapy)
- Esophageal Squamous Cell Carcinoma
(blood, pathology, therapy)
- Female
- Gas Chromatography-Mass Spectrometry
- Humans
- Male
- Metabolome
- Metabolomics
(methods)
- Middle Aged
- Neoadjuvant Therapy
(methods)
- Neoplasm Staging
- Prospective Studies
- Treatment Outcome
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