Abstract

Exopolysaccharide produced by Lactiplantibacillus plantarum-12 (LPEPS) exhibited the anti-proliferating effect on human colon cancer cell line HT-29 in vitro. The purpose of the study was to determine the alleviating effects of LPEPS on colon cancer development of the C57BL/6 mice treated by azoxymethane/dextran sulfate sodium salt (AOM/DSS). The C57BL/6 mice treated by AOM/DSS were orally administered LPEPS daily for 85 days. The results showed that LPEPS oral administration enhanced colon tight-junction protein expression and ameliorated colon shortening and tumor burden of the AOM/DSS treated mice. Furthermore, LPEPS oral administration significantly reduced pro-inflammatory factors TNF-α, IL-8, and IL-1β levels and increased anti-inflammatory factor IL-10 level in the serum of the AOM/DSS-treated mice. LPEPS oral administration reversed the alterations of gut flora in AOM/DSS-treated mice, as evidenced by the increasing of the abundance of Bacteroidetes, Bacteroidetes/Firmicutes ratio, Muribaculaceae, Burkholderiaceae, and norank_o__Rhodospirillales and the decreasing of the abundance of Firmicutes, Desulfovibrionaceae, Erysipelotrichaceae, and Helicobacteraceae. The fecal metabolites of the AOM/DSS-treated mice were altered by LPEPS oral administration, involving lipid metabolism and amino acid metabolism. Together, these results suggested that LPEPS oral administration alleviated AOM/DSS-induced colon cancer symptoms of the C57BL/6 mice by modulating gut microbiota and metabolites, enhancing intestine barrier, inhibiting NF-κB pathway, and activating caspase cascade.

Highlights

  • Colon cancer is the most common cancer of human beings

  • Colon cancer patients are accompanied by gut microbiota composition dysbiosis, including the decrease of the diversity of gut microbiota, the increase of the abundance of potentially harmful bacteria, and the decrease of the abundance of beneficial bacteria, which leads to gut metabolite changes and intestinal inflammation

  • The results showed that LPEPS oral administration could modulate the intestinal flora and fecal metabolites, enhance intestinal barrier, and alleviate colon inflammation and colon tumor in azoxymethane/dextran sulfate sodium salt (AOM/dextran sulfate sodium salt (DSS))-treated C57BL/6 mice

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Summary

Introduction

Colon cancer is the most common cancer of human beings. The incidence and mortality of patients with colon cancer is ranked third and second, respectively [1]. Colon cancer is seriously threatening human health and brings many adverse effects on human beings. A number of previous studies have shown that intestinal flora and metabolites of patients with colon cancer are different from those of healthy individuals [2,3,4]. Colon cancer patients are accompanied by gut microbiota composition dysbiosis, including the decrease of the diversity of gut microbiota, the increase of the abundance of potentially harmful bacteria, and the decrease of the abundance of beneficial bacteria, which leads to gut metabolite changes and intestinal inflammation. Previous studies have demonstrated that IBD is an important cause of colon cancer [6]

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