The Interplay between Microbiota and Chemotherapy-Derived Metabolites in Breast Cancer

Author:

Plaza-Diaz Julio123ORCID,Álvarez-Mercado Ana Isabel124ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology II, School of Pharmacy, University of Granada, 18071 Granada, Spain

2. Instituto de Investigación Biosanitaria ibs.GRANADA, Complejo Hospitalario Universitario de Granada, 18014 Granada, Spain

3. Children’s Hospital of Eastern Ontario Research Institute, Ottawa, ON K1H 8L1, Canada

4. Institute of Nutrition and Food Technology, Biomedical Research Center, University of Granada, 18016 Armilla, Spain

Abstract

The most common cancer in women is breast cancer, which is also the second leading cause of death in this group. It is, however, important to note that some women will develop or will not develop breast cancer regardless of whether certain known risk factors are present. On the other hand, certain compounds are produced by bacteria in the gut, such as short-chain fatty acids, secondary bile acids, and other metabolites that may be linked to breast cancer development and mediate the chemotherapy response. Modeling the microbiota through dietary intervention and identifying metabolites directly associated with breast cancer and its complications may be useful to identify actionable targets and improve the effect of antiangiogenic therapies. Metabolomics is therefore a complementary approach to metagenomics for this purpose. As a result of the combination of both techniques, a better understanding of molecular biology and oncogenesis can be obtained. This article reviews recent literature about the influence of bacterial metabolites and chemotherapy metabolites in breast cancer patients, as well as the influence of diet.

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference182 articles.

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5. National Cancer Institute (NCI) (2023, March 17). Breast Cancer Treatment, Available online: https://www.cancer.gov/types/breast/hp/breast-treatment-pdq.

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