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Identification of Diagnostic Metabolic Signatures in Thyroid Tumors Using Mass Spectrometry Imaging

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2023 Aug 12
PMID 37570761
Authors
Affiliations
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Abstract

"Gray zone" thyroid follicular tumors are difficult to diagnose, especially when distinguishing between benign follicular thyroid adenoma (FTA) and malignant carcinoma (FTC). Thus, proper classification of thyroid follicular diseases may improve clinical prognosis. In this study, the diagnostic performance of metabolite enzymes was evaluated using imaging mass spectrometry to distinguish FTA from FTC and determine the association between metabolite enzyme expression with thyroid follicular borderline tumor diagnosis. Air flow-assisted desorption electrospray ionization mass spectrometry imaging (AFAIDESI-MSI) was used to build a classification model for thyroid follicular tumor characteristics among 24 samples. We analyzed metabolic enzyme marker expression in an independent validation set of 133 cases and further evaluated the potential biological behavior of 19 thyroid borderline lesions. Phospholipids and fatty acids (FAs) were more abundant in FTA than FTC ( < 0.001). The metabolic enzyme panel, which included FA synthase and Ca-independent PLA2, was further validated in follicular thyroid tumors. The marker combination showed optimal performance in the validation group (area under the ROC, sensitivity, and specificity: 73.6%, 82.1%, and 60.6%, respectively). The findings indicate that AFAIDESI-MSI, in combination with low metabolic enzyme expression, could play a role in the diagnosis of thyroid follicular borderline tumors for strict follow-up.

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References
1.
Korbecki J, Bosiacki M, Gutowska I, Chlubek D, Baranowska-Bosiacka I . Biosynthesis and Significance of Fatty Acids, Glycerophospholipids, and Triacylglycerol in the Processes of Glioblastoma Tumorigenesis. Cancers (Basel). 2023; 15(7). PMC: 10093493. DOI: 10.3390/cancers15072183. View

2.
Zhang X, Zhao C, Seleznev K, Song K, Manfredi J, Ma Z . Disruption of G1-phase phospholipid turnover by inhibition of Ca2+-independent phospholipase A2 induces a p53-dependent cell-cycle arrest in G1 phase. J Cell Sci. 2006; 119(Pt 6):1005-15. PMC: 2917323. DOI: 10.1242/jcs.02821. View

3.
Zhang X, Zhao C, Ma Z . The increase of cell-membranous phosphatidylcholines containing polyunsaturated fatty acid residues induces phosphorylation of p53 through activation of ATR. J Cell Sci. 2007; 120(Pt 23):4134-43. PMC: 2915541. DOI: 10.1242/jcs.015834. View

4.
Siegel R, Miller K, Jemal A . Cancer statistics, 2019. CA Cancer J Clin. 2019; 69(1):7-34. DOI: 10.3322/caac.21551. View

5.
Song Y, Wilkins P, Hu W, Murthy K, Chen J, Lee Z . Inhibition of calcium-independent phospholipase A2 suppresses proliferation and tumorigenicity of ovarian carcinoma cells. Biochem J. 2007; 406(3):427-36. PMC: 2049037. DOI: 10.1042/BJ20070631. View