4.7 Review

Next-generation probiotics - do they open new therapeutic strategies for cancer patients?

Journal

GUT MICROBES
Volume 14, Issue 1, Pages -

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/19490976.2022.2035659

Keywords

Gut microbiota; next-generation probiotics; Faecalibacterium prausnitzii; Akkermansia muciniphila; Bacteroides fragilis; cancer; immunotherapy

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The gut microbiota has been extensively studied in relation to cancer development and treatment. Next-generation probiotics (NGPs) are being increasingly explored as therapeutic agents that can alter the gut microbiota and impact cancer development. This review focuses on three emerging NGPs – Faecalibacterium prausnitzii, Akkermansia muciniphila, and Bacteroides fragilis – which have been found to have an impact on cancer incidence. These NGPs enhance gastrointestinal immunity, maintain intestinal barrier integrity, produce beneficial metabolites, act against pathogens, improve immunotherapy efficacy, and reduce complications associated with chemotherapy and radiotherapy. While the safety of NGPs in cancer patients is still relatively unclear, recent data has shown that they are non-toxigenic. Overall, the use of NGPs shows promise in preventing cancer development and providing new therapeutic options for cancer patients.
Gut microbiota and its association with cancer development/treatment has been intensively studied during the past several years. Currently, there is a growing interest toward next-generation probiotics (NGPs) as therapeutic agents that alter gut microbiota and impact on cancer development. In the present review we focus on three emerging NGPs, namely Faecalibacterium prausnitzii, Akkermansia muciniphila, and Bacteroides fragilis as their presence in the digestive tract can have an impact on cancer incidence. These NGPs enhance gastrointestinal immunity, maintain intestinal barrier integrity, produce beneficial metabolites, act against pathogens, improve immunotherapy efficacy, and reduce complications associated with chemotherapy and radiotherapy. Notably, the use of NGPs in cancer patients does not have a long history and, although their safety remains relatively undefined, recently published data has shown that they are non-toxigenic. Notwithstanding, A. muciniphila may promote colitis whereas enterotoxigenic B. fragilis stimulates chronic inflammation and participates in colorectal carcinogenesis. Nevertheless, the majority of B. fragilis strains provide a beneficial effect to the host, are non-toxigenic and considered as the best current NGP candidate. Overall, emerging studies indicate a beneficial role of these NGPs in the prevention of carcinogenesis and open new promising therapeutic options for cancer patients.

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