A Free Amino Acid Diet Alleviates Colorectal Tumorigenesis through Modulating Gut Microbiota and Metabolites.
Yang-Meng YuGui-Fang LiYi-Lin RenXin-Yi XuZheng-Hong XuYan GengYong MaoPublished in: Nutrients (2024)
Colorectal cancer (CRC), a major global health concern, may be influenced by dietary protein digestibility impacting gut microbiota and metabolites, which is crucial for cancer therapy effectiveness. This study explored the effects of a casein protein diet (CTL) versus a free amino acid (FAA)-based diet on CRC progression, gut microbiota, and metabolites using carcinogen-induced (AOM/DSS) and spontaneous genetically induced ( Apc Min/+ mice) CRC mouse models. Comprehensive approaches including 16s rRNA gene sequencing, transcriptomics, metabolomics, and immunohistochemistry were utilized. We found that the FAA significantly attenuated CRC progression, evidenced by reduced colonic shortening and histopathological alterations compared to the CTL diet. Notably, the FAA enriched beneficial gut bacteria like Akkermansia and Bacteroides and reversed CRC-associated dysbiosis. Metabolomic analysis highlighted an increase in ornithine cycle metabolites and specific fatty acids, such as Docosapentaenoic acid (DPA), in FAA-fed mice. Transcriptomic analysis revealed that FAA up-regulated Egl-9 family hypoxia inducible factor 3 (Egln 3) and downregulated several cancer-associated pathways including Hippo, mTOR, and Wnt signaling. Additionally, DPA was found to significantly induce EGLN 3 expression in CRC cell lines. These results suggest that FAA modulate gut microbial composition, enhance protective metabolites, improve gut barrier functions, and inhibit carcinogenic pathways.
Keyphrases
- amino acid
- ms ms
- weight loss
- physical activity
- global health
- single cell
- cancer therapy
- high glucose
- mouse model
- diabetic rats
- fatty acid
- poor prognosis
- high fat diet induced
- randomized controlled trial
- systematic review
- public health
- mass spectrometry
- drug delivery
- oxidative stress
- type diabetes
- cell proliferation
- gene expression
- binding protein
- drug induced
- transcription factor
- signaling pathway
- microbial community
- adipose tissue
- genome wide
- polycyclic aromatic hydrocarbons