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dc.contributor.authorRodilla, Ananda M.
dc.contributor.authorKorrodi Gregório, Luís
dc.contributor.authorHernando Santa Cruz, Elsa 
dc.contributor.authorManuel Manresa, Pilar .
dc.contributor.authorQuesada Pato, Roberto 
dc.contributor.authorPérez Tomás, Ricardo
dc.contributor.authorSoto Cerrato, Vanessa
dc.date.accessioned2017-03-09T09:35:27Z
dc.date.available2018-02-01T03:45:06Z
dc.date.issued2017-02
dc.identifier.urihttp://hdl.handle.net/10259/4353
dc.description.abstractCurrent pharmacological treatments for lung cancer show very poor clinical outcomes, therefore, the development of novel anticancer agents with innovative mechanisms of action is urgently needed. Cancer cells have a reversed pH gradient compared to normal cells, which favours cancer progression by promoting proliferation, metabolic adaptation and evasion of apoptosis. In this regard, the use of ionophores to modulate intracellular pH appears as a promising new therapeutic strategy. Indeed, there is a growing body of evidence supporting ionophores as novel antitumour drugs. Despite this, little is known about the implications of pH deregulation and homeostasis imbalance triggered by ionophores at the cellular level. In this work, we deeply analyse for the first time the anticancer effects of tambjamine analogues, a group of highly effective anion selective ionophores, at the cellular and molecular levels. First, their effects on cell viability were determined in several lung cancer cell lines and patient-derived cancer stem cells, demonstrating their potent cytotoxic effects. Then, we have characterized the induced lysosomal deacidification, as well as, the massive cytoplasmic vacuolization observed after treatment with these compounds, which is consistent with mitochondrial swelling. Finally, the activation of several proteins involved in stress response, autophagy and apoptosis was also detected, although they were not significantly responsible for the cell death induced. Altogether, these evidences suggest that tambjamine analogues provoke an imbalance in cellular ion homeostasis that triggers mitochondrial dysfunction and lysosomal deacidification leading to a potent cytotoxic effect through necrosis in lung cancer cell lines and cancer stem cells.en
dc.description.sponsorshipSpanish government and the EU (FIS PI13/00089), Consejería de Educación de la Junta de Castilla y León (BU340U13 and BU092U16).en
dc.format.mimetypeapplication/pdf
dc.language.isoenges
dc.publisherElsevieren
dc.relation.ispartofBiochemical Pharmacology. 2017. V. 126, p. 23–33en
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAnionophoresen
dc.subjectSynthetictambjamine analoguesen
dc.subjectLysosomal dysfunctionen
dc.subjectAutophagy blockadeen
dc.subjectNecrosisen
dc.subject.otherChemistry, Organicen
dc.subject.otherQuímica orgánicaes
dc.titleSynthetic tambjamine analogues induce mitochondrial swelling and lysosomal dysfunction leading to autophagy blockade and necrotic cell death in lung canceren
dc.typeinfo:eu-repo/semantics/article
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.relation.publisherversionhttp://dx.doi.org/10.1016/j.bcp.2016.11.022
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersionen


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