4.7 Article

Intestinal vitamin D receptor protects against extraintestinal breast cancer tumorigenesis

Journal

GUT MICROBES
Volume 15, Issue 1, Pages -

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/19490976.2023.2202593

Keywords

Dysbiosis; breast cancer; barrier function; butyrate-producing bacteria; butyrate; inflammation; gut-breast-axis; Lactobacillus plantarum; probiotics; tight junctions; VDR

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The microbiota plays a critical role in regulating intestinal and extraintestinal health. This study investigates the potential connection between the intestinal microbiome and breast cancer. Through the examination of mice with VDR deficiency and dysbiosis, the researchers found that VDR deficiency leads to an increased susceptibility to breast cancer. Moreover, they identified the mechanisms by which VDR deficiency disrupts gut health and increases the risk of breast tumorigenesis. Treatment with beneficial bacteria or their metabolites showed promising results in reducing breast tumors and improving gut health.
The microbiota plays critical roles in regulating the function and health of the intestine and extraintestinal organs. A fundamental question is whether an intestinal-microbiome-breast axis exists during the development of breast cancer. If so, what are the roles of host factors? Vitamin D receptor (VDR) involves host factors and the human microbiome. Vdr gene variation shapes the human microbiome, and VDR deficiency leads to dysbiosis. We hypothesized that intestinal VDR protects hosts against tumorigenesis in the breast. We examined a 7,12-dimethylbenzanthracene (DMBA)-induced breast cancer model in intestinal epithelial VDR knockout (VDR Delta IEC) mice with dysbiosis. We reported that VDR Delta IEC mice with dysbiosis are more susceptible to breast cancer induced by DMBA. Intestinal and breast microbiota analysis showed that VDR deficiency leads to a bacterial profile shift from normal to susceptible to carcinogenesis. We found enhanced bacterial staining within breast tumors. At the molecular and cellular levels, we identified the mechanisms by which intestinal epithelial VDR deficiency led to increased gut permeability, disrupted tight junctions, microbial translocation, and enhanced inflammation, thus increasing tumor size and number in the breast. Furthermore, treatment with the beneficial bacterial metabolite butyrate or the probiotic Lactobacillus plantarum reduced breast tumors, enhanced tight junctions, inhibited inflammation, increased butyryl-CoA transferase, and decreased levels of breast Streptococcus bacteria in VDR Delta IEC mice. The gut microbiome contributes to the pathogenesis of diseases not only in the intestine but also in the breast. Our study provides insights into the mechanism by which intestinal VDR dysfunction and gut dysbiosis lead to a high risk of extraintestinal tumorigenesis. Gut-tumor-microbiome interactions represent a new target in the prevention and treatment of breast cancer.

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