4.6 Article

Rearrangements of Blood and Tissue Fatty Acid Profile in Colorectal Cancer-Molecular Mechanism and Diagnostic Potential

Journal

FRONTIERS IN ONCOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2021.689701

Keywords

colorectal cancer; gas chromatography-mass spectrometry; fatty acid; lipids; PCA; PLS-DA

Categories

Funding

  1. National Science Centre of Poland [2016/22/E/NZ4/00665]
  2. Medical University of Gdansk [ST-40, ST-89]

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The study found that colorectal cancer patients have significantly higher levels of very long chain fatty acids in cancer tissue and serum, which are absent in healthy individuals. A panel of fatty acids identified in a single analysis can effectively distinguish colorectal cancer patients from healthy subjects.
Colorectal cancer (CRC) is often diagnosed at an advanced stage due to the invasiveness of colonoscopy; thus, non-invasive CRC diagnostics are desirable. CRC is associated with lipid alterations. We aimed to verify whether fatty acid (FA) profiles in CRC patients may serve as a potential diagnostic tool for CRC diagnosis. FA profiles were assayed by GC-MS in cancer tissue, paired normal mucosa and serum from CRC patients and healthy controls. The levels of very long FAs - VLCFAs (26:0, 28:0 and 26:1) were the most highly increased FAs in cancer tissue compared to normal colon mucosa. Moreover, these FA were present in serum of CRC patients, they were absent in the serum of healthy subjects, or present in only trace amounts. To verify if cancer cells are the source of small amounts of these VLCFAs in the serum of patients we performed experiment in HT-29 CRC cells, which proved that CRC cells can produce and release VLCFAs into the blood. Most importantly, we defined a panel of FAs that may be assayed in a single analysis that definitely distinguishes CRC patients and healthy subjects, which was confirmed by PLS-DA and multivariate ROC analysis (AUC = 0.985). This study shows that selected FA panel may serve as a diagnostic marker for CRC.

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