Affiliation:
1. Department of General Surgery Peking University Third Hospital Beijing 100191 P. R. China
2. Cancer Center Peking University Third Hospital Beijing 100191 P. R. China
3. State Key Laboratory of Women's Reproductive Health and Fertility Promotion Peking University Beijing 100191 P. R. China
4. Department of Endocrinology and Metabolism Peking University Third Hospital Beijing 100191 P. R. China
5. Center of Basic Medical Research Institute of Medical Innovation and Research Third Hospital Peking University Beijing 100191 P. R. China
6. Department of Physiology and Pathophysiology School of Basic Medical Sciences Peking University and the Key Laboratory of Molecular Cardiovascular Science (Peking University) Ministry of Education Beijing 100191 P. R. China
7. Center for Obesity and Metabolic Disease Research School of Basic Medical Sciences Peking University Beijing 100191 P. R. China
Abstract
AbstractColorectal cancer (CRC) is the most common cancer of the digestive system with high mortality and morbidity rates. Gut microbiota is found in the intestines, especially the colorectum, and has structured crosstalk interactions with the host that affect several physiological processes. The gut microbiota include CRC‐promoting bacterial species, such as Fusobacterium nucleatum, Escherichia coli, and Bacteroides fragilis, and CRC‐protecting bacterial species, such as Clostridium butyricum, Streptococcus thermophilus, and Lacticaseibacillus paracasei, which along with other microorganisms, such as viruses and fungi, play critical roles in the development of CRC. Different bacterial features are identified in patients with early‐onset CRC, combined with different patterns between fecal and intratumoral microbiota. The gut microbiota may be beneficial in the diagnosis and treatment of CRC; some bacteria may serve as biomarkers while others as regulators of chemotherapy and immunotherapy. Furthermore, metabolites produced by the gut microbiota play essential roles in the crosstalk with CRC cells. Harmful metabolites include some primary bile acids and short‐chain fatty acids, whereas others, including ursodeoxycholic acid and butyrate, are beneficial and impede tumor development and progression. This review focuses on the gut microbiota and its metabolites, and their potential roles in the development, diagnosis, and treatment of CRC.
Funder
National Key Research and Development Program of China
National Natural Science Foundation of China
Subject
General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)
Cited by
41 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献