Docosahexaenoic acid (DHA) inhibits pro-angiogenic effects of breast cancer cells via down-regulating cellular and exosomal expression of angiogenic genes and microRNAs

Docosahexaenoic acid (DHA) as an omega 3 free fatty acid has been reported to exert anti-angiogenesis effects. However, our current understanding regarding the precise mechanisms of such effects is still limited. Exosomes secreted by cancer cells may act as angiogenesis promoters. The aim of the stu...

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Veröffentlicht in:Life sciences (1973) 2020-10, Vol.258, p.118094, Article 118094
Hauptverfasser: Aslan, Cynthia, Maralbashi, Sepideh, Kahroba, Houman, Asadi, Milad, Soltani-Zangbar, Mohammad Sadegh, Javadian, Mahsa, Shanehbandi, Dariush, Baradaran, Behzad, Darabi, Masood, Kazemi, Tohid
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Sprache:eng
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Zusammenfassung:Docosahexaenoic acid (DHA) as an omega 3 free fatty acid has been reported to exert anti-angiogenesis effects. However, our current understanding regarding the precise mechanisms of such effects is still limited. Exosomes secreted by cancer cells may act as angiogenesis promoters. The aim of the study was to determine altered expression levels of HIF-1α, TGF-β, VEGFR, Snail1, Snail2 and SOX2 and their regulating microRNAs in MDA-MB-231 and BT-474 cell lines after treatment with DHA in both normoxic and hypoxic conditions. Human breast cancer cell lines including MDA-MB-231 and BT-474 were treated for 24 h with 100 uM DHA under normoxic and hypoxic conditions. Exosomes were isolated from untreated and treated cells and characterized by transmission electron microscopy (TEM) and western blotting. RNAs from cells and isolated exosomes were extracted and cDNAs were synthesized. Expression levels of miRNAs and their pro-angiogenic target genes were analyzed using quantitative real-time PCR (qRT-PCR). We showed significant decrease in the expression of pro-angiogenic genes including HIF1-α, TGF-β, SOX2, Snail1, Snail2 and VEGFR in cells and also their secreted exosomes after treatment with DHA in normoxic and hypoxic conditions. Also the expression levels of tumor suppressor miRs including miR-101, miR-199, miR-342 were increased and the expression levels of oncomiRs including mir-382 and miR-21 were decreased after treatment with DHA in cells and exosomes. DHA can alter the expression of pro-angiogenic genes and microRNA contents in breast cancer cells and their derived-exosomes in favor of the inhibition of angiogenesis. Our data demonstrated new insight into DHA's anti-cancer action to target not only breast cancer cells but also their derived exosomes to suppress tumor angiogenesis. DHA has potent anti-angiogenic effects in breast cancer cells via down regulating expression of several angiogenic factors and also changing the contents of exosomes to convey anti-angiogenic effects of DHA to target cells. [Display omitted] •Tumor-derived exosomes contain multiple pro-angiogenic cargoes.•DHA alters the contents of exosomes, besides cancer cells.•Exosomes can mediate DHA's anti-angiogenic action to target cells.
ISSN:0024-3205
1879-0631
DOI:10.1016/j.lfs.2020.118094