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September 10, 2025Nutrients17 citationsOpen Access

Gut-Microbiota-Derived Metabolites and Probiotic Strategies in Colorectal Cancer: Implications for Disease Modulation and Precision Therapy

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YYYi-Chu YangSCShih-Chang ChangCHChih‐Sheng Hung

Key Points

  • Probiotics may enhance gut barrier integrity and reduce inflammation, impacting colorectal cancer outcomes.
  • Short-chain fatty acids, particularly butyrate, have anti-inflammatory and anti-cancer properties crucial for gut health.
  • Dysbiosis connects gut microbiota imbalance to conditions like colorectal cancer, underscoring the role of microbial therapies.
  • A tailored approach to microbiome medicine can support preventive and personalized healthcare strategies.

Abstract

The human gut microbiota significantly influences host health through its metabolic products and interaction with immune, neural, and metabolic systems. Among these, short-chain fatty acids (SCFAs), especially butyrate, play key roles in maintaining gut barrier integrity, modulating inflammation, and supporting metabolic regulation. Dysbiosis is increasingly linked to diverse conditions such as gastrointestinal, metabolic, and neuropsychiatric disorders, cardiovascular diseases, and colorectal cancer (CRC). Probiotics offer therapeutic potential by restoring microbial balance, enhancing epithelial defenses, and modulating immune responses. This review highlights the physiological functions of gut microbiota and SCFAs, with a particular focus on butyrate’s anti-inflammatory and anti-cancer effects in CRC. It also examines emerging microbial therapies like probiotics, synbiotics, postbiotics, and engineered microbes. Emphasis is placed on the need for precision microbiome medicine, tailored to individual host–microbiome interactions and metabolomic profiles. These insights underscore the promising role of gut microbiota modulation in advancing preventive and personalized healthcare.

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Cite This Study

Yang et al. (2025) studied this question.

synapsesocial.com/papers/68c19f9c54b1d3bfb60db584https://doi.org/10.3390/nu17152501
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