Gut microbiota-derived bile acids in intestinal immunity, inflammation, and tumorigenesis
Inflammatory bowel disease (IBD) and colorectal cancer (CRC) are heterogeneous intestinal diseases that threaten the health of an increasing number of individuals as their lifestyles become westernized. New insights have been discovered with the development of various omics techniques, revealing tha...
Saved in:
Published in | Cell host & microbe Vol. 30; no. 3; pp. 289 - 300 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
09.03.2022
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Inflammatory bowel disease (IBD) and colorectal cancer (CRC) are heterogeneous intestinal diseases that threaten the health of an increasing number of individuals as their lifestyles become westernized. New insights have been discovered with the development of various omics techniques, revealing that gut-microbiota-derived metabolites play important roles in maintaining intestinal homeostasis and modulating the progression of intestinal diseases from both metabolic and immunological perspectives. Clinical metagenomic and metabolomic studies have revealed links between microbial bile acid (BA) metabolism and IBD and CRC progression. Several BA-derived metabolites were recently been demonstrated to play a role in intestinal immunity, providing fresh insights into how BAs affect the course of IBD and CRC. In this review, we discuss recent studies on the involvement of gut microbiota-derived BAs in intestinal immunity, inflammation, and tumorigenesis along with human omics data to provide prospective insights into future prevention and treatment of IBD and CRC. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 AUTHOR CONTRIBUTIONS Equal contribution Writing – Original Draft, J.C.; Visualization, L.S.; Writing – Review & Editing, J.C., L.S, F.J.G.; Supervision – F.J.G. |
ISSN: | 1931-3128 1934-6069 1934-6069 |
DOI: | 10.1016/j.chom.2022.02.004 |