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Metabolomic Profiling Identifies Biomarkers and Metabolic Impacts of Surgery for Colorectal Cancer

Overview
Journal Front Surg
Specialty General Surgery
Date 2022 Sep 12
PMID 36090329
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Abstract

Background: Colorectal cancer (CRC) is one of the most common malignant tumors with recurrence and metastasis after surgical resection. This study aimed to identify the physiological changes after surgery and explore metabolites and metabolic pathways with potential prognostic value for CRC.

Methods: An ultra-high-performance liquid chromatography Q-exactive mass spectrometry was used to profile serum metabolites from 67 CRC patients and 50 healthy volunteers. Principal component analysis (PCA) and orthogonal projections to latent structures-discriminant analysis were used to distinguish the internal characteristics of data in different groups. Multivariate statistics were compiled to screen the significant metabolites and metabolic pathways.

Result: A total of 180 metabolites were detected. Under the conditions of variable importance in projection >1 and -value <0.05, 46 differentially expressed metabolites were screened for further pathway enrichment analysis. Based on the Kyoto Encyclopedia of Genes and Genomes database and Small Molecule Pathway Database, three metabolic pathways-arginine and proline metabolism, ascorbate and aldarate metabolism, and phenylalanine metabolism-were significantly altered after surgical resection and identified as associated with the removal of CRC. Notably, gamma-linolenic acid was upregulated in the CRC preoperative patients compared with those in healthy volunteers but returned to healthy levels after surgery.

Conclusion: Through serum-based metabolomics, our study demonstrated the differential metabolic characteristics in CRC patients after surgery compared with those before surgery. Our results suggested that metabonomic analysis may be a powerful method for exploring physiological alterations in CRC patients after surgery as well as a useful tool for identifying candidate biomarkers and monitoring disease recurrence.

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References
1.
Neurauter G, Grahmann A, Klieber M, Zeimet A, Ledochowski M, Sperner-Unterweger B . Serum phenylalanine concentrations in patients with ovarian carcinoma correlate with concentrations of immune activation markers and of isoprostane-8. Cancer Lett. 2008; 272(1):141-7. DOI: 10.1016/j.canlet.2008.07.002. View

2.
Chas M, Goupille C, Arbion F, Bougnoux P, Pinault M, Jourdan M . Low eicosapentaenoic acid and gamma-linolenic acid levels in breast adipose tissue are associated with inflammatory breast cancer. Breast. 2019; 45:113-117. DOI: 10.1016/j.breast.2019.04.001. View

3.
Liu C, Chen W, Lin C, Liu H, Chen H, Yang P . Topology-based cancer classification and related pathway mining using microarray data. Nucleic Acids Res. 2006; 34(14):4069-80. PMC: 1557825. DOI: 10.1093/nar/gkl583. View

4.
Sahu N, Dela Cruz D, Gao M, Sandoval W, Haverty P, Liu J . Proline Starvation Induces Unresolved ER Stress and Hinders mTORC1-Dependent Tumorigenesis. Cell Metab. 2016; 24(5):753-761. DOI: 10.1016/j.cmet.2016.08.008. View

5.
Ma Y, Chapman J, Levine M, Polireddy K, Drisko J, Chen Q . High-dose parenteral ascorbate enhanced chemosensitivity of ovarian cancer and reduced toxicity of chemotherapy. Sci Transl Med. 2014; 6(222):222ra18. DOI: 10.1126/scitranslmed.3007154. View