TY - JOUR
T1 - Anticancer effects of the microbiome and its products
AU - Zitvogel, Laurence
AU - Daillère, Romain
AU - Roberti, María Paula
AU - Routy, Bertrand
AU - Kroemer, Guido
N1 - Publisher Copyright:
© 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.
PY - 2017/8/1
Y1 - 2017/8/1
N2 - The human gut microbiome modulates many host processes, including metabolism, inflammation, and immune and cellular responses. It is becoming increasingly apparent that the microbiome can also influence the development of cancer. In preclinical models, the host response to cancer treatment has been improved by modulating the gut microbiome; this is known to have an altered composition in many diseases, including cancer. In addition, cancer treatment with microbial agents or their products has the potential to shrink tumours. However, the microbiome could also negatively influence cancer prognosis through the production of potentially oncogenic toxins and metabolites by bacteria. Thus, future antineoplastic treatments could combine the modulation of the microbiome and its products with immunotherapeutics and more conventional approaches that directly target malignant cells.
AB - The human gut microbiome modulates many host processes, including metabolism, inflammation, and immune and cellular responses. It is becoming increasingly apparent that the microbiome can also influence the development of cancer. In preclinical models, the host response to cancer treatment has been improved by modulating the gut microbiome; this is known to have an altered composition in many diseases, including cancer. In addition, cancer treatment with microbial agents or their products has the potential to shrink tumours. However, the microbiome could also negatively influence cancer prognosis through the production of potentially oncogenic toxins and metabolites by bacteria. Thus, future antineoplastic treatments could combine the modulation of the microbiome and its products with immunotherapeutics and more conventional approaches that directly target malignant cells.
UR - http://www.scopus.com/inward/record.url?scp=85023641634&partnerID=8YFLogxK
U2 - 10.1038/nrmicro.2017.44
DO - 10.1038/nrmicro.2017.44
M3 - Review article
C2 - 28529325
AN - SCOPUS:85023641634
SN - 1740-1526
VL - 15
SP - 465
EP - 478
JO - Nature Reviews Microbiology
JF - Nature Reviews Microbiology
IS - 8
ER -