4.7 Article

San-Wu-Huang-Qin decoction attenuates tumorigenesis and mucosal barrier impairment in the AOM/DSS model by targeting gut microbiome

Journal

PHYTOMEDICINE
Volume 98, Issue -, Pages -

Publisher

ELSEVIER GMBH
DOI: 10.1016/j.phymed.2022.153966

Keywords

Colorectal cancer; Tumorigenesis; Gut microbiota; Chinese Herbals; San-Wu-Huang-Qin decoction

Funding

  1. National Natural Science Foundation of China [81830120]
  2. Shanghai Frontier Research Base of Disease and Syndrome Biology of Inflammatory Cancer Trans-formation [2021KJ03-12]
  3. Clinical Research Plan of SHDC [SHDC2020CR4047]
  4. Health and Family Planning Scientific Research Project Plan [pw2020d-4]
  5. Project of Shanghai [19401972200]

Ask authors/readers for more resources

In this study, it was demonstrated that San-Wu-Huang-Qin decoction effectively inhibits tumorigenesis and protects the mucosal barrier in colorectal cancer (CRC) at least partially by targeting gut microbiota. This research provides a scientific basis for the clinical usage of San-Wu-Huang-Qin decoction in the intervention and prevention of CRC.
Background: A classic herbal formula San-Wu-Huang-Qin (SWHQ) decoction has been widely used in clinical practices to prevent and treat colorectal cancer (CRC) for years, but its anti-tumorigenic properties and the underlying mechanisms remain undetermined. Purpose: The present study used a CRC mouse model to clarify whether and how SWHQ suppresses tumorigenesis. Methods: Different doses of SWHQ were gavaged to the AOM/DSS model mice to examine its anti-tumor efficacy in comparison with the positive control drug Aspirin. The underlying microbiota-driven anti-tumor action of SWHQ was proven with bacterial manipulations by fecal microbial transplantation (FMT) in vivo and anaerobic culturing in vitro. Results: SWHQ decoction dose-dependently reduced colonic tumor numbers/loads of AOM/DSS models and suppressed their disease activity index scores. SWHQ also recovered epithelial MUC2 secretion and colonic tight junction protein (ZO-1 and claudin1) expression in the mouse model. Such inhibitory impact on tumorigenesis and mucosal barrier impairment was found to be associated with modulation of gut dysbiosis, particularly for suppressing lipopolysaccharide (LPS) producers. The FMT experiment confirmed the substantial contribution of SWHQ-reshaped microbiota to anti-tumor function and mucosal barrier protection. Moreover, LPS-activated TLR4/NF-kappa B signaling and its downstream pro-inflammatory factors were significantly suppressed in the colon of SWHQ-treated models and SWHQ-reshaped microbiota recipients. Conclusions: We demonstrated that the SWHQ effectively inhibited tumorigenesis and protect mucosal barrier in CRC at least partially by targeting gut microbiota. This study provides scientific basis for the clinical usage of SWHQ in CRC intervention and prevention.

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