Bovine holo-lactoferrin inhibits migration and invasion in MDA-MB-231 breast cancer cells

Purpose Breast cancer is the most common malignancy in developed countries and the main cause of deaths in women worldwide. Lactoferrin (Lf) is an iron-binding protein constituted for a single polypeptide chain that is folded into two symmetrical lobes that bind Fe 2+ or Fe 3+ . Lf has the ability t...

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Veröffentlicht in:Molecular biology reports 2023-01, Vol.50 (1), p.193-201
Hauptverfasser: Rodriguez-Ochoa, Ninive, Cortes-Reynosa, Pedro, Rodriguez-Rojas, Karem, de la Garza, Mireya, Salazar, Eduardo Perez
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Sprache:eng
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Zusammenfassung:Purpose Breast cancer is the most common malignancy in developed countries and the main cause of deaths in women worldwide. Lactoferrin (Lf) is an iron-binding protein constituted for a single polypeptide chain that is folded into two symmetrical lobes that bind Fe 2+ or Fe 3+ . Lf has the ability to reversibly bind Fe 3+ and is found free of Fe 3+ (Apo-Lf) or associated with Fe 3+ (Holo-Lf) with a different three-dimensional conformation. However, the role of bovine Apo-Lf (Apo-BLf) and bovine Holo-Lf (Holo-BLf) in the migration and invasion induced by linoleic acid (LA) and fetal bovine serum (FBS), as well as in the expression of mesenchymal and epithelial proteins in breast cancer cells has not been studied. Methods and results Scratch wound assays demonstrated that Holo-BLf and Apo-BLf do not induce migration, however they differentially inhibit the migration induced by FBS and LA in breast cancer cells MDA-MB-231. Western blot, invasion, zymography and immunofluorescence confocal microscopy assays demonstrated that Holo-BLf partly inhibit the invasion, FAK phosphorylation at tyrosine (Tyr)-397 and MMP-9 secretion, whereas it increased the number and size of focal adhesions induced by FBS in MDA-MB-231 cells. Moreover, Holo-BLf induced a slight increase of E-cadherin expression in MCF-7 cells, and inhibited vimentin expression in MCF-7 and MDA-MB-231 breast cancer cells. Conclusion Holo-BLf inhibits cellular processes that mediate the invasion process in breast cancer cells.
ISSN:0301-4851
1573-4978
DOI:10.1007/s11033-022-07943-8