Garlic Polysaccharides Ameliorate AOM/DSS-Induced Colon Tumorigenesis: A Multi-Omics Mechanistic Study

Yongqiu Qi1, Xiaoming Lu1, Lingyu Li1

  • 1Key Laboratory of Food Nutrition and Health in Universities of Shandong, College of Food Science and Engineering, Shandong Agricultural University, 61 Daizong Street, Tai'an 271018, China.

Insights

Garlic polysaccharides (GP-1) show significant anti-tumor effects against colon cancer in mice. This natural compound promotes gut health by regulating microbiota and reducing inflammation.

Area of Science:

  • Gastroenterology
  • Oncology
  • Immunology

Background:

  • Natural plant polysaccharides are recognized for their prebiotic properties and beneficial effects on inflammation, tumors, immunity, and gut microbiota.
  • Garlic polysaccharides (GP-1) are explored for their potential health benefits.

Purpose of the Study:

  • To investigate the anti-tumor effects of garlic polysaccharides (GP-1) in a mouse model of colitis-associated colon tumorigenesis.
  • To elucidate the underlying mechanisms of GP-1's anti-tumor activity.

Main Methods:

  • A mouse model of azoxymethane/dextran sulfate sodium-induced colitis-associated colon tumorigenesis was utilized.
  • Garlic polysaccharides (GP-1), identified as a fructan, were administered to tumor-bearing mice.
  • Multi-omics analyses were performed to understand the molecular mechanisms.

Main Results:

  • GP-1 significantly improved survival rates, reduced colon tumor burden, and alleviated intestinal bleeding.
  • Intestinal damage was attenuated, with enhanced barrier integrity, reduced pro-inflammatory cytokines, and increased antioxidant enzyme activity.
  • GP-1 inhibited aberrant epithelial proliferation by suppressing Ki67 protein expression and modulated gut microbiota and metabolites.

Conclusions:

  • Garlic polysaccharides (GP-1) exhibit a notable inhibitory effect on colon tumorigenesis.
  • GP-1 demonstrates potential as a functional food ingredient for promoting gut health and combating colon cancer.

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