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Published on: December 26, 2016
Bacterial metabolites: Effects on the development of breast cancer and therapeutic efficacy (Review)
Yan Guo1, Wenyan Dong2, Dezheng Sun2
1Department of Endocrinology, Changhai Hospital, Naval Medical University, Shanghai 200433, P.R. China.
Abstract:
Evidence suggests that various gut metabolites significantly impact breast cancer (BC) and its treatment. However, the underlying mechanisms remain poorly understood and require further investigation. In the present study, the current literature was reviewed to evaluate the roles of microbial metabolites in the development of BC and its response to treatment. Microbial metabolites, including secondary bile acids, short-chain fatty acids, amino acid metabolites, lipopolysaccharide, nisin and pyocyanin, serve crucial roles in the BC microenvironment. Microbial metabolites promote BC invasion, metastasis and recurrence by facilitating cellular movement, epithelial-mesenchymal transition, cancer stem cell function and diapedesis. Furthermore, certain metabolites, such as trimethylamine N-oxide and L-norvaline, can alter the pharmacokinetics of chemotherapeutic drugs. The present review highlights the possible involvement of microbial metabolites and bacteriocins in BC carcinogenesis, development and metastasis. These metabolites could provide new insights for BC treatment strategies and are considered potential therapeutic targets.
Insights
Gut microbial metabolites significantly influence breast cancer (BC) development and treatment response. Understanding these roles offers potential new therapeutic targets for BC.
Area of Science:
- Microbiology
- Oncology
- Metabolomics
Background:
- Gut metabolites play a significant role in breast cancer (BC) and its treatment.
- The precise mechanisms by which these metabolites influence BC are not fully understood.
Purpose of the Study:
- To review the current literature on the roles of microbial metabolites in breast cancer (BC) development and treatment response.
- To evaluate the impact of specific microbial metabolites on the BC microenvironment and disease progression.
Main Methods:
- Literature review of existing studies on gut microbial metabolites and breast cancer.
- Analysis of the mechanisms by which metabolites affect BC invasion, metastasis, and recurrence.
- Examination of metabolite interactions with chemotherapeutic drug pharmacokinetics.
Main Results:
- Microbial metabolites such as secondary bile acids, short-chain fatty acids, and others are crucial in the BC microenvironment.
- These metabolites promote BC invasion, metastasis, and recurrence by affecting cellular movement, epithelial-mesenchymal transition, cancer stem cell function, and diapedesis.
- Certain metabolites (e.g., trimethylamine N-oxide, L-norvaline) can alter the pharmacokinetics of chemotherapy drugs.
Conclusions:
- Microbial metabolites and bacteriocins are implicated in BC carcinogenesis, development, and metastasis.
- These findings suggest potential new insights for BC treatment strategies.
- Microbial metabolites represent promising therapeutic targets for breast cancer.
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