Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/42765

TitleLactoferrin selectively triggers apoptosis in highly metastatic breast cancer cells through inhibition of plasmalemmal V-H+-ATPase
Author(s)Pereira, Cátia S.
Guedes, J.
Gonçalves, Marília
Loureiro, Luís
Castro, Lisandra
Gerós, Hernâni
Rodrigues, L. R.
Côrte-Real, Manuela
KeywordsLactoferrin
V-H+-ATPase
breast cancer
V-H+-ATPase inhibitor
extracellular acidification rate
Issue date19-Aug-2016
PublisherImpact Journals
JournalOncotarget
CitationCátia S. Pereira; Guedes, J.; Gonçalves, Marília; Loureiro, Luís; Castro, Lisandra; Gerós, Hernâni; Rodrigues, Lígia R.; Côrte-Real, Manuela, Lactoferrin selectively triggers apoptosis in highly metastatic breast cancer cells through inhibition of plasmalemmal V-H+-ATPase. Oncotarget, 7(38), 62144-62158, 2016
Abstract(s)Breast cancer is the most common type of cancer affecting women. Despite the good prognosis when detected early, significant challenges remain in the treatment of metastatic breast cancer. The recruitment of the vacuolar H+-ATPase (V-H+-ATPase) to the plasma membrane, where it mediates the acidification of the tumor microenvironment (TME), is a recognized feature involved in the acquisition of a metastatic phenotype in breast cancer. Therefore, inhibitors of this pump have emerged as promising anticancer drugs. Lactoferrin (Lf) is a natural pro-apoptotic iron-binding glycoprotein with strong anticancer activity whose mechanism of action is not fully understood. Here, we show that bovine Lf (bLf) preferentially induces apoptosis in the highly metastatic breast cancer cell lines Hs 578T and MDA-MB-231, which display a prominent localisation of V-H+-ATPase at the plasma membrane, but not in the lowly metastatic T-47D or in the non-tumorigenic MCF-10-2A cell lines. We also demonstrate that bLf decreases the extracellular acidification rate and causes intracellular acidification in metastatic breast cancer cells and, much like the well-known proton pump inhibitors concanamycin A and bafilomycin A1, inhibits V-H+-ATPase in sub-cellular fractions. These data further support that bLf targets V-H+-ATPase and explain the selectivity of bLf for cancer cells, especially for highly metastatic breast cancer cells. Altogether, our results pave the way for more rational in vivo studies aiming to explore this natural non-toxic compound for metastatic breast cancer therapy.
TypeArticle
URIhttp://hdl.handle.net/1822/42765
DOI10.18632/oncotarget.11394
ISSN1949-2553
e-ISSN1949-2553
Publisher versionhttp://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=index
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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