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dc.contributor.authorPark, Sang-Hyun
dc.contributor.authorHwang, Inhong
dc.contributor.authorMcNaughton, Daniel A.
dc.contributor.authorKinross, Airlie J.
dc.contributor.authorHowe, Ethan N.W.
dc.contributor.authorXiong, Shenglun
dc.contributor.authorKilde, Martin Drøhse
dc.contributor.authorLynch, Vincent M.
dc.contributor.authorGale, Philip A.
dc.contributor.authorSessler, Jonathan L.
dc.contributor.authorShin, Injae
dc.contributor.authorHe, Qing
dc.date.accessioned2022-01-19T01:06:05Z
dc.date.available2022-01-19T01:06:05Z
dc.date.issued2021en
dc.identifier.urihttps://hdl.handle.net/2123/27336
dc.description.abstractA number of artificial cation ionophores (or transporters) have been developed for basic research and biomedical applications. However, their mechanisms of action and the putative correlations between changes in intracellular cation concentrations and induced cell death remain poorly understood. Here we show that three hemispherand-strapped calix[4]pyrrole based ion pair receptors act as efficient Na+/K+ exchangers in the presence of Cl- in liposomal models, and promote Na+ influx and K+ efflux (Na+/K+ exchange) in cancer cells to induce apoptosis. Mechanistic studies reveal that these cation exchangers induce endoplasmic reticulum (ER) stress in cancer cells by perturbing intracellular cation homeostasis, promote generation of reactive oxygen species, and eventually enhance mitochondria-mediated apoptosis. However, they neither induce osmotic stress nor affect autophagy. The present study provides support for the notion that synthetic receptors which perturb cellular cation homeostasis may provide a new approach to generating agents with potentially useful apoptotic activity.en
dc.language.isoenen
dc.publisherCell Pressen
dc.relation.ispartofChemical Communicationsen
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0en
dc.subjectcation transporten
dc.subjectsupramolecular chemistryen
dc.titleSynthetic Na+/K+ exchangers promote apoptosis by disturbing cellular cation homeostasisen
dc.typeArticleen
dc.subject.asrc0399 Other Chemical Sciencesen
dc.identifier.doi10.1016/j.chempr.2021.08.018
dc.type.pubtypeAuthor accepted manuscripten
dc.relation.arcDP200100453
usyd.facultySeS faculties schools::Faculty of Science::School of Chemistryen
usyd.facultySeS faculties schools::The University of Sydney Multidisciplinary Centres and Institutes::The University of Sydney Nano Instituteen
usyd.citation.volume7en
usyd.citation.issue12en
usyd.citation.spage3325en
usyd.citation.epage3339en
workflow.metadata.onlyNoen


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