Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/81276

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dc.contributor.authorFogde, Ditte L.por
dc.contributor.authorXavier, Cristina P. R.por
dc.contributor.authorBalnyte, Kristinapor
dc.contributor.authorHolland, Lya K. K.por
dc.contributor.authorStahl-Meyer, Kamillapor
dc.contributor.authorDinant, Christoffelpor
dc.contributor.authorCorcelle-Termeau, Elisabethpor
dc.contributor.authorPereira-Wilson, Cristinapor
dc.contributor.authorMaeda, Kenjipor
dc.contributor.authorJäättelä, Marjapor
dc.date.accessioned2022-12-20T09:23:44Z-
dc.date.available2022-12-20T09:23:44Z-
dc.date.issued2022-12-14-
dc.identifier.citationFogde, D.L.; Xavier, C.P.R.; Balnytė, K.; Holland, L.K.K.; Stahl-Meyer, K.; Dinant, C.; Corcelle-Termeau, E.; Pereira-Wilson, C.; Maeda, K.; Jäättelä, M. Ursolic Acid Impairs Cellular Lipid Homeostasis and Lysosomal Membrane Integrity in Breast Carcinoma Cells. Cells 2022, 11, 4079. https://doi.org/10.3390/cells11244079por
dc.identifier.urihttps://hdl.handle.net/1822/81276-
dc.descriptionThe following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/cells11244079/s1, Figure S1: UA kills MCF7 cells partly through apoptosis; Figure S2: UA causes LC3 puncta formation in MCF7 and HCT15 cells; Figure S3: UA causes LMP prior to MOMP and alters lysosomal localization in HeLa cells; Figure S4: Additional lipidomics data; Table S1: List of resources; Table S2: Internal lipid and drug standards; Table S3: Precursor ion, fragment ion, and neutral loss for lipid identification; Table S4: All experiments.por
dc.description.abstractCancer is one of the leading causes of death worldwide, thus the search for new cancer therapies is of utmost importance. Ursolic acid is a naturally occurring pentacyclic triterpene with a wide range of pharmacological activities including anti-inflammatory and anti-neoplastic effects. The latter has been assigned to its ability to promote apoptosis and inhibit cancer cell proliferation by poorly defined mechanisms. In this report, we identify lysosomes as the essential targets of the anti-cancer activity of ursolic acid. The treatment of MCF7 breast cancer cells with ursolic acid elevates lysosomal pH, alters the cellular lipid profile, and causes lysosomal membrane permeabilization and leakage of lysosomal enzymes into the cytosol. Lysosomal membrane permeabilization precedes the essential hallmarks of apoptosis placing it as an initial event in the cascade of effects induced by ursolic acid. The disruption of the lysosomal function impairs the autophagic pathway and likely partakes in the mechanism by which ursolic acid kills cancer cells. Furthermore, we find that combining treatment with ursolic acid and cationic amphiphilic drugs can significantly enhance the degree of lysosomal membrane permeabilization and cell death in breast cancer cells.por
dc.description.sponsorshipThis work was supported by grants from the Danish National Research Foundation (DNRF125), European Research Council (AdG340751), Danish Cancer Society (R167-A11061) and, Novo Nordisk Foundation (NNF19OC0054296), to M.J., K.M. was supported by the Independent Research Fund Denmark (6108–00542B) and Novo Nordisk Foundation (NNF17OC0029432).por
dc.language.isoengpor
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)por
dc.rightsopenAccesspor
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/por
dc.subjectAutophagypor
dc.subjectCationic amphiphilic drugspor
dc.subjectCell deathpor
dc.subjectCancerpor
dc.subjectLysosomal membrane permeabilizationpor
dc.subjectUrsolic acidpor
dc.titleUrsolic acid impairs cellular lipid homeostasis and lysosomal membrane integrity in breast carcinoma cellspor
dc.typearticle-
dc.peerreviewedyespor
dc.relation.publisherversionhttps://www.mdpi.com/journal/cellspor
dc.commentsCEB55989por
oaire.citationStartPage4079por
oaire.citationIssue24por
oaire.citationConferencePlaceSwitzerland-
oaire.citationVolume11por
dc.date.updated2022-12-19T18:45:02Z-
dc.identifier.eissn2073-4409por
dc.identifier.doi10.3390/cells11244079por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersion-
dc.subject.wosScience & Technologypor
sdum.journalCellspor
oaire.versionVoRpor
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DBio - Artigos/Papers

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