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Abstract Title:

Hydroxytyrosol inhibits cancer stem cells and the metastatic capacity of triple-negative breast cancer cell lines by the simultaneous targeting of epithelial-to-mesenchymal transition, Wnt/β-catenin and TGFβ signaling pathways.

Abstract Source:

Eur J Nutr. 2018 Nov 21. Epub 2018 Nov 21. PMID: 30460610

Abstract Author(s):

Marina Cruz-Lozano, Adrián González-González, Juan A Marchal, Esperanza Muñoz-Muela, Maria P Molina, Francisca E Cara, Anthony M Brown, Gerardo García-Rivas, Carmen Hernández-Brenes, Jose A Lorente, Pedro Sanchez-Rovira, Jenny C Chang, Sergio Granados-Principal

Article Affiliation:

Marina Cruz-Lozano

Abstract:

PURPOSE: This study was aimed to determine the impact of hydroxytyrosol (HT), a minor compound found in olive oil, on breast cancer stem cells (BCSCs) and the migration capacity of triple-negative breast cancer (TNBC) cell lines through the alteration of epithelial-to-mesenchymal transition (EMT) and embryonic signaling pathways.

METHODS: BCSCs self-renewal was determined by the mammosphere-forming efficiency in SUM159PT, BT549, MDA-MB-231 and Hs578T TNBC cell lines. Flow cytometric analysis of CD44/CD24and aldehyde dehydrogenase positive (ALDH) subpopulations, migration by the"wound healing assay", invasion and Western blot of EMT markers and TGFβ signaling were investigated in SUM159PT, BT549 and MDA-MB-231 cell lines. Wnt/β-catenin signaling was assessed by Western blot in BT549 cells expressing WNT1 and MDA-MB-231 cells. Changes in TGFβ activity was determined by SMAD Binding Element (SBE) reporter assay.

RESULTS: HT reduced BCSCs self-renewal, ALDH(aldehyde dehydrogenase) and CD44/CD24subpopulations, tumor cell migration and invasion. Consistently, HT suppressed Wnt/β-catenin signaling by decreasing p-LRP6, LRP6, β-catenin and cyclin D1 protein expression and the EMT markers SLUG, ZEB1, SNAIL and VIMENTIN. Finally, HT inhibited p-SMAD2/3 and SMAD2/3 in SUM159PT, BT549 and MDA-MB-231 cells, what was correlated with a less TGFβ activity.

CONCLUSION: In conclusion, we report for the first time the inhibitory role of HT on BCSCs and tumor cell migration by targeting EMT, Wnt/β-catenin and TGFβ signaling pathways. Our findings highlight the importance of the chemopreventive compound HT as a novel candidate to be investigated as an alternative targeted therapy for TNBC.

Study Type : In Vitro Study

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Sayer Ji
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