Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/40324

TitleTargeting lactate transport suppresses in vivo breast tumour growth.
Author(s)Moreira, António Herculano Jesus
Pinheiro, Céline
Baltazar, Fátima
Vilaça, João L.
Longatto Filho, Adhemar
Santos, Luísa Filipa Morais dos
Queirós, Sandro Filipe Monteiro
Granja, Sara Costa
Gonçalves, Vera M.
KeywordsMonocarboxylate transporters
Breast carcinoma
Hypoxia
Lactate
Warburg effect
Issue date18-Aug-2015
PublisherImpact Journals LLC
JournalOncotarget
CitationMorais-Santos, F., Granja, S., Miranda-Goncalves, V., Moreira, A. H. J., Queiros, S., Vilaca, J. L., . . . Pinheiro, C. (2015). Targeting lactate transport suppresses in vivo breast tumour growth. Oncotarget, 6(22), 19177-19189.
Abstract(s)BACKGROUND Most cancers, including breast cancer, have high rates of glucose consumption, associated with lactate production, a process referred as "Warburg effect". Acidification of the tumour microenvironment by lactate extrusion, performed by lactate transporters (MCTs), is associated with higher cell proliferation, migration, invasion, angiogenesis and increased cell survival. Previously, we have described MCT1 up-regulation in breast carcinoma samples and demonstrated the importance of in vitro MCT inhibition. In this study, we performed siRNA knockdown of MCT1 and MCT4 in basal-like breast cancer cells in both normoxia and hypoxia conditions to validate the potential of lactate transport inhibition in breast cancer treatment. RESULTS The effect of MCT knockdown was evaluated on lactate efflux, proliferation, cell biomass, migration and invasion and induction of tumour xenografts in nude mice. MCT knockdown led to a decrease in in vitro tumour cell aggressiveness, with decreased lactate transport, cell proliferation, migration and invasion and, importantly, to an inhibition of in vivo tumour formation and growth. CONCLUSIONS This work supports MCTs as promising targets in cancer therapy, demonstrates the contribution of MCTs to cancer cell aggressiveness and, more importantly, shows, for the first time, the disruption of in vivo breast tumour growth by targeting lactate transport.
TypeArticle
URIhttp://hdl.handle.net/1822/40324
DOI10.18632/oncotarget.3910
ISSN1949-2553
Publisher versionhttp://www.impactjournals.com/oncotarget/index.php?journal=oncotarget&page=article&op=view&path%5B%5D=3910&path%5B%5D=11694
Peer-Reviewedyes
AccessOpen access
Appears in Collections:ICVS - Artigos em Revistas Internacionais com Referee

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