Issue 14, 2025

Gut microbial metabolites of phenolic compounds inhibit colon cancer cell proliferation by triggering apoptosis and cell cycle arrest

Abstract

Growing evidence shows how diet can influence the onset of colon cancer. In this regard, phenolic compounds, and particularly, their metabolites produced by the gut microbiota, may be responsible for this protective effect. Therefore, in this study, some of the main gut microbial metabolites of phenolic compounds were tested for their anti-proliferative activity against two colon adenocarcinoma cell lines (Caco-2 and SW480). Two compounds, 3′,4′-dihydroxyphenylacetic acid and 3-(3′,4′-dihydroxyphenyl)propanoic acid, showed IC50 values towards Caco-2 below the physiological concentrations found in the colon. In addition, other compounds showing low IC50 values towards Caco-2 were 2,3,4-trihyroxybenzoic acid (gallic acid), 1,2,3-trihydroxybenzene (pyrogallol), and 5-(3′,4′-dihydroxyphenyl)-γ-valerolactone. Whereas three flavanone aglycones (naringenin, eriodictyol, and hesperetin) and, again, 2,3,4-trihyroxybenzoic acid, and 1,2,3-trihydroxybenzene were the most active towards SW480. Some compounds exert an anti-proliferative effect by disrupting the cell cycle, others by inducing apoptosis, and others by promoting reactive oxygen species formation. Thus, this study demonstrates that gut microbial metabolites of phenolic compounds can be held responsible for the protective effect against the onset of colon cancer of a diet rich in fruit and vegetables.

Graphical abstract: Gut microbial metabolites of phenolic compounds inhibit colon cancer cell proliferation by triggering apoptosis and cell cycle arrest

Article information

Article type
Paper
Submitted
12 May 2025
Accepted
23 Jun 2025
First published
24 Jun 2025

Food Funct., 2025,16, 5836-5849

Gut microbial metabolites of phenolic compounds inhibit colon cancer cell proliferation by triggering apoptosis and cell cycle arrest

M. Zannini, M. De Angeli, A. Conte, V. Minischetti, D. D'Arca, D. Tagliazucchi and A. Cattivelli, Food Funct., 2025, 16, 5836 DOI: 10.1039/D5FO02116B

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