4.8 Article

High-salt diet inhibits tumour growth in mice via regulating myeloid-derived suppressor cell differentiation

Journal

NATURE COMMUNICATIONS
Volume 11, Issue 1, Pages -

Publisher

NATURE RESEARCH
DOI: 10.1038/s41467-020-15524-1

Keywords

-

Funding

  1. National Key Research and Development Programme of China [2017YFC0909702]
  2. National Natural Science Foundation of China [81973273, 81673380, 31971309, 31671031]
  3. Jiangsu Province Funds for Distinguished Young Scientists [BK20170015]
  4. Fundamental Research Funds for the Central Universities [020814380115]
  5. Science and Technology Development Fund, Macau SAR (FDCT) [080/2016/A2, 0018/2019/AFJ, 0097/2019/A2]
  6. University of Macau [MYRG2017-00028-ICMS]
  7. Natural Science Foundation of China [31961160701]
  8. Science and Technology Development Fund [31961160701]
  9. Anhui provincial Natural Science Foundation [1908085QC131]
  10. Grants for Scientific Research of BSKY from Anhui Medical University [XJ201726]

Ask authors/readers for more resources

High-salt intake can promote pro-inflammatory responses associated with pathological conditions. However, here, the authors show that high-salt diet may have an antitumor protective role by modulating the accumulation and phenotype of myeloid derived suppressor cells and enhancing immunosurveillance. High-salt diets are associated with an elevated risk of autoimmune diseases, and immune dysregulation plays a key role in cancer development. However, the correlation between high-salt diets (HSD) and cancer development remains unclear. Here, we report that HSD increases the local concentration of sodium chloride in tumour tissue, inducing high osmotic stress that decreases both the production of cytokines required for myeloid-derived suppressor cells (MDSCs) expansion and MDSCs accumulation in the blood, spleen, and tumour. Consequently, the two major types of MDSCs change their phenotypes: monocytic-MDSCs differentiate into antitumour macrophages, and granulocytic-MDSCs adopt pro-inflammatory functions, thereby reactivating the antitumour actions of T cells. In addition, the expression of p38 mitogen-activated protein kinase-dependent nuclear factor of activated T cells 5 is enhanced in HSD-induced M-MDSC differentiation. Collectively, our study indicates that high-salt intake inhibits tumour growth in mice by activating antitumour immune surveillance through modulating the activities of MDSCs.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available