Potential influence of the microbiome environment in patients with biliary tract cancer and implications for therapy
Authors
Wheatley, RoseannaKilgour, Elaine
Jacobs, Timothy
Lamarca, Angela
Hubner, Richard A
Valle, Juan W
McNamara, Mairead G
Affiliation
Division of Cancer Sciences, School of Medical Sciences, Faculty of Biology Medicine and Health, The University of Manchester, ManchesterIssue Date
2021
Metadata
Show full item recordAbstract
Biliary tract cancers, including intra- and extra-hepatic cholangiocarcinoma as well as gallbladder cancer, are associated with poor prognosis and the majority of patients present with advanced-stage, non-resectable disease at diagnosis. Biliary tract cancer may develop through an accumulation of genetic and epigenetic alterations and can be influenced by microbial exposure. Furthermore, the liver and biliary tract are exposed to the gastrointestinal microbiome through the gut-liver axis. The availability of next-generation sequencing technology has led to an increase in studies investigating the relationship between microbiota and human disease. In particular, the interplay between the microbiome, the tumour micro-environment and response to systemic therapy is a prospering area of interest. Given the poor outcomes for patients with biliary tract cancer, this emerging field of research, through which new biomarkers may be identified, offers potential as a tool for early diagnosis, prognostication or even as a future therapeutic target. This review summarises the available evidence on the microbiome environment in patients with biliary tract cancer, including a discussion around confounding factors, implications for therapy and proposed future directions.Citation
Wheatley RC, Kilgour E, Jacobs T, Lamarca A, Hubner RA, Valle JW, et al. Potential influence of the microbiome environment in patients with biliary tract cancer and implications for therapy. British Journal of Cancer. Springer Science and Business Media LLC; 2021.Journal
British Journal of CancerDOI
10.1038/s41416-021-01583-8PubMed ID
34663949Additional Links
https://dx.doi.org/10.1038/s41416-021-01583-8Type
ArticleLanguage
enae974a485f413a2113503eed53cd6c53
10.1038/s41416-021-01583-8
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