Linoleic acid induces secretion of extracellular vesicles from MDA-MB-231 breast cancer cells that mediate cellular processes involved with angiogenesis in HUVECs
[Display omitted] •Extracellular vesicles from breast cancer cells mediate angiogenesis.•Linoleic acid induces release of angiogenic extracellular vesicles.•FFAR1 and FFAR4 mediate the release of angiogenic extracellular vesicles. Extracellular vesicles (EVs) are vesicles secreted by normal and mali...
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Veröffentlicht in: | Prostaglandins & other lipid mediators 2021-04, Vol.153, p.106519, Article 106519 |
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Sprache: | eng |
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•Extracellular vesicles from breast cancer cells mediate angiogenesis.•Linoleic acid induces release of angiogenic extracellular vesicles.•FFAR1 and FFAR4 mediate the release of angiogenic extracellular vesicles.
Extracellular vesicles (EVs) are vesicles secreted by normal and malignant cells that are implicated in tumor progression. Linoleic acid (LA) is an essential polyunsaturated fatty acid that induces migration, invasion and an increase in phospholipase D activity in breast cancer cells. In this study, we determined whether stimulation of MDA-MB-231 breast cancer cells with LA induces the secretion of EVs, which can mediate cell processes related with angiogenesis in human umbilical vein endothelial cells (HUVECs). Our findings demonstrate that treatment of MDA-MB-231 cells with 90 μM LA for 48 h induce an increase in the number of EVs released. Moreover, EVs from MDA-MB-231 stimulated with 90 μM LA induce FAK and Src activation and migration via FAK and Src activity, whereas the secretion of these EVs is through FFAR1 and FFAR4 activation in HUVECs. The EVs from MDA-MB-231 cells treated with LA also increase proliferation, invasion, MMP-9 secretion, an increase of MMP-2 secretion and formation of new tubules in HUVECs. In summary, we demonstrate, for the first time, that treatment with LA induces the release of EVs from MDA-MB-231 cells that induce cellular processes involved with angiogenesis in HUVECs. |
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ISSN: | 1098-8823 |
DOI: | 10.1016/j.prostaglandins.2020.106519 |