The impact of the host intestinal microbiome on carcinogenesis and the response to chemotherapy

Future Oncol. 2021 Nov;17(32):4371-4387. doi: 10.2217/fon-2021-0087. Epub 2021 Aug 27.

Abstract

The microbiome consists of all microbes present on and within the human body. An unbalanced, or 'dysbiotic' intestinal microbiome is associated with inflammatory bowel disease, diabetes and some cancer types. Drug treatment can alter the intestinal microbiome composition. Additionally, some chemotherapeutics interact with microbiome components, leading to changes in drug safety and/or efficacy. The intestinal microbiome is a modifiable target, using strategies such as antibiotic treatment, fecal microbial transplantation or probiotic administration. Understanding the impact of the microbiome on the safety and efficacy of cancer treatment may result in improved treatment outcome. The present review seeks to summarize relevant research and look to the future of cancer treatment, where the intestinal microbiome is recognized as an actionable treatment target.

Keywords: cancer; chemotherapy; drug efficacy; drug safety; microbiome; pharmacomicrobiomics; probiotics.

Plain language summary

Lay abstract The microbiome describes all of the microorganisms (including bacteria, viruses and fungi) that are normally present on and inside the human body. Some diseases, including cancer, can be caused or worsened by an ‘unbalanced’ or ‘unhealthy’ gut microbiome. Some drugs that are given to people who have cancer can change the microbiome. Importantly, components of the gut microbiome can also change how a cancer drug will work in someone. We can change the microbiome in certain ways, like by giving someone antibiotics. Understanding how the microbiome influences the way anticancer drugs work is important because it could help us understand how to make cancer treatment safer and more effective. This review article summarizes available research on the impact of the microbiome on cancer treatment.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / adverse effects
  • Asparaginase / therapeutic use
  • Carcinogenesis
  • Gastrointestinal Microbiome / drug effects
  • Gastrointestinal Microbiome / physiology*
  • Humans
  • Immune Checkpoint Inhibitors / pharmacology
  • Neoplasms / drug therapy
  • Neoplasms / etiology*
  • Neoplasms / microbiology

Substances

  • Antineoplastic Agents
  • Immune Checkpoint Inhibitors
  • Asparaginase