Application of microbial metabolite in tumor immune response and microbial metabolite screening method

By constructing a screening system for PD-1/SHP-2 pathway signal transduction, intestinal microbial metabolites such as glycine deoxycholic acid and taurocholic acid were screened out, which solved the problem of insufficient immune response in colorectal cancer in existing technologies and achieved enhanced treatment effects for colorectal cancer.

CN120939227APending Publication Date: 2025-11-14ZHEJIANG PROVINCIAL PEOPLES HOSPITAL
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Patent Information

Application Number
CN202510929567.5
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-07-07
Publication Date
2025-11-14

AI Technical Summary

Technical Problem

In existing technologies, there are relatively few types of gut microbial metabolites that affect the immune response to colorectal cancer, and their effects are relatively weak. More effective metabolites need to be screened out to enhance the efficacy of colorectal cancer immunotherapy.

Method used

A screening system based on PD-1/SHP-2 pathway signal transduction was constructed. By binding firefly luciferase to PD-1/SHP-2, intestinal microbial metabolites such as glycodeoxycholic acid (GDCA) and taurocholic acid (TCA) were screened out to inhibit T cell function and promote tumor growth. Effective metabolites were screened out by luciferase activity assay.

Benefits of technology

A reliable, rapid, and effective screening and evaluation system was established, and gut microbial metabolites that affect the PD-1 signaling pathway were discovered and validated, which enhanced the immune response to colorectal cancer and provided experimental evidence for the treatment of colorectal cancer.

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Abstract

The invention provides application of microbial metabolites in tumor immune response and an intestinal microbial metabolite screening method. A screening system is constructed by combining firefly luciferase with PD-1 / SHP-2, various intestinal microbial metabolites are independently co-cultured with the screening system, the screened microbial metabolites are glycodeoxycholic acid and taurocholic acid, and the influence of various metabolites on PD-1 pathway signal transduction is reflected by measuring the activity of luciferase. The invention constructs a reliable, rapid and effective screening method for discovering intestinal microbial metabolites influencing a PD-1 signal channel and evaluating the influence efficacy of the metabolites, and screening out metabolites having effects on intestinal cancer immune response, thereby providing an experimental basis for enhancing intestinal cancer treatment.
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