dc.creatorCárdenas, César
dc.creatorMüller, Marioly
dc.creatorMcNeal, Andrew
dc.creatorLovy, Alenka
dc.creatorJaňa, Fabian
dc.creatorBustos, Galdo
dc.creatorUrra, Felix
dc.creatorSmith, Natalia
dc.creatorMolgó, Jordi
dc.creatorDiehl, J. Alan
dc.creatorRidky, Todd W.
dc.creatorFoskett, J. Kevin
dc.date.accessioned2019-03-18T11:53:50Z
dc.date.available2019-03-18T11:53:50Z
dc.date.created2019-03-18T11:53:50Z
dc.date.issued2016
dc.identifierCell Reports, Volumen 14, Issue 10, 2018, Pages 2313-2324
dc.identifier22111247
dc.identifier10.1016/j.celrep.2016.02.030
dc.identifierhttps://repositorio.uchile.cl/handle/2250/166747
dc.description.abstract© 2016 The Authors.In the absence of low-level ER-to-mitochondrial Ca2+ transfer, ATP levels fall, and AMPK-dependent, mTOR-independent autophagy is induced as an essential survival mechanism in many cell types. Here, we demonstrate that tumorigenic cancer cell lines, transformed primary human fibroblasts, and tumors in vivo respond similarly but that autophagy is insufficient for survival, and cancer cells die while their normal counterparts are spared. Cancer cell death is due to compromised bioenergetics that can be rescued with metabolic substrates or nucleotides and caused by necrosis associated with mitotic catastrophe during their proliferation. Our findings reveal an unexpected dependency on constitutive Ca2+ transfer to mitochondria for viability of tumorigenic cells and suggest that mitochondrial Ca2+ addiction is a feature of cancer cells. Cárdenas et al. show that inhibition of low-level ER-to-mitochondria Ca2+ transfer is toxic, specifically to cancer cells. Their study re
dc.languageen
dc.publisherElsevier B.V.
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceCell Reports
dc.subjectBiochemistry, Genetics and Molecular Biology (all)
dc.titleSelective Vulnerability of Cancer Cells by Inhibition of Ca2+ Transfer from Endoplasmic Reticulum to Mitochondria
dc.typeArtículos de revistas


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