关键词: Antineoplastic antimetabolites Cancer Gut microbiota Individualized medication Probiotics

Mesh : Animals Antimetabolites, Antineoplastic / pharmacokinetics therapeutic use toxicity Food-Drug Interactions / physiology Gastrointestinal Microbiome / drug effects physiology Humans Neoplasms / drug therapy metabolism Probiotics / administration & dosage pharmacokinetics Treatment Outcome

来  源:   DOI:10.1016/j.tox.2021.152858   PDF(Sci-hub)

Abstract:
The incidence and mortality of cancer are rapidly growing all over the world. Nowadays, antineoplastic antimetabolites still play a key role in the chemotherapy of cancer. However, the interindividual variations in the efficacy and toxicity of antineoplastic antimetabolites are nonnegligible challenges to their clinical applications. Although many studies have focused on genetic variation, the reasons for these interindividual variations have still not been fully understood. Gut microbiota is reported to be associated with the efficacy and toxicity of antineoplastic antimetabolites. In this review, we summarize the interaction of antineoplastic antimetabolites on gut microbiota and the influences of shifted gut microbiota profiles on the efficacy and toxicity of antineoplastic antimetabolites. The factors affecting the efficacy and toxicity of antineoplastic antimetabolites via gut microbiota are also discussed. In addition, we present our viewpoints that regulating the gut microbiota may increase the efficacy and decrease the toxicity of antineoplastic antimetabolites. This will help us better understand the new mechanism via gut microbiota and promote individualized use of antineoplastic antimetabolites.
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