4.6 Article

Carcinoma associated fibroblasts small extracellular vesicles with low miR-7641 promotes breast cancer stemness and glycolysis by HIF-1α

Journal

CELL DEATH DISCOVERY
Volume 7, Issue 1, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41420-021-00524-x

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Funding

  1. National Natural Science Foundation of China [81502571]
  2. Shanghai Science and Technology Committee [19140901000]
  3. Natural Science Foundation of Shanghai [19ZR1410000]

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The study revealed that sEVs from cancer-associated fibroblasts play a crucial role in breast cancer progression through the miR-7641/HIF-1 alpha pathway, suppressing breast cancer cell survival, glycolysis, and stem cell properties. This provides a potential new approach for targeting breast cancer.
Fibroblasts play an important role in cancer development and progression. Small extracellular vesicles (sEVs) are one type of extracellular vesicles, which mediate the interaction between cancer-associated fibroblasts and cancer cells by transferring their contents. However, the roles of sEVs from cancer-associated fibroblasts on breast cancer stem cell properties are largely unraveled. The purpose of this study was to explore the roles of sEVs from cancer-associated fibroblasts on breast cancer progression. The miRNA array data showed a different miRNA profile between CAFs sEVs and normal fibroblasts sEVs. By verification using real-time RT-PCR, the data analysis indicated that miR-7641 levels were lower in sEVs from CAFs compared with NFs. The cellular functions were assayed and the results indicated that CAFs derived sEVs with low miR-7641 levels suppressed breast cancer cell survival, glycolysis, and stem cell properties via the HIF-1 alpha pathway. Collectively, these findings indicated that sEVs from CAFs promoted breast cancer stem cell properties and glycolysis via miR-7641/HIF-1 alpha, which was a possible new way for targeting breast cancer.

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