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Exploring the impact of gut microbiota and diet on breast cancer risk and progression

期刊

INTERNATIONAL JOURNAL OF CANCER
卷 149, 期 3, 页码 494-504

出版社

WILEY
DOI: 10.1002/ijc.33496

关键词

antibiotics; breast cancer; diet; immune; microbiota

类别

资金

  1. BigC Cancer Charity [17-16R, 18-15R]
  2. Biotechnology and Biological Sciences Research Council [BB/R012490/1, BBS/E/F/000PR10353, BBS/E/F/000PR10356]
  3. Breast Cancer Now [2017NovPhD973]
  4. Wellcome Trust [100/974/C/13/Z]
  5. BBSRC [BBS/E/F/00044409, BBS/E/F/000PR10355, BBS/E/F/000PR10356, BBS/E/F/000PR10353] Funding Source: UKRI

向作者/读者索取更多资源

The microbiota plays a key role in cancer outcomes and responses, although breast cancer has been relatively understudied compared to other types of cancer. Environmental factors like diet and antibiotics can impact the microbiota and influence breast cancer outcomes. In-depth studies on the microbiota-Breast Cancer relationship and the underlying mechanisms are still needed to fully understand these complex interactions.
There is emerging evidence that resident microbiota communities, that is, the microbiota, play a key role in cancer outcomes and anticancer responses. Although this has been relatively well studied in colorectal cancer and melanoma, other cancers, such as breast cancer (BrCa), have been largely overlooked to date. Importantly, many of the environmental factors associated with BrCa incidence and progression are also known to impact the microbiota, for example, diet and antibiotics. Here, we explore BrCa risk factors from large epidemiology studies and microbiota associations, and more recent studies that have directly profiled BrCa patients' gut microbiotas. We also discuss how in vivo studies have begun to unravel the immune mechanisms whereby the microbiota may influence BrCa responses, and finally we examine how diet and specific nutrients are also linked to BrCa outcomes. We also consider future research avenues and important considerations with respect to study design and implementation, and we highlight some of the important unresolved questions, which currently limit our overall understanding of the mechanisms underpinning microbiota-BrCa responses.

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