Identification of a Noncanonical Necrotic Cell Death Triggered Via Enhanced Proteolysis by a Novel Sapogenol Derivative

dc.contributor.author Üner, Göklem
dc.contributor.author Tağ, Özgür
dc.contributor.author Erzurumlu, Yalçın
dc.contributor.author Ballar Kırmızıbayrak, Petek
dc.contributor.author Bedir, Erdal
dc.coverage.doi 10.1021/acs.chemrestox.0c00339
dc.date.accessioned 2021-01-24T18:33:14Z
dc.date.available 2021-01-24T18:33:14Z
dc.date.issued 2020
dc.description.abstract Small molecules which activate distinct cell death pathways have promising high potential for anticancer drug research. Especially, regulated necrosis draws attention as an alternative cell death mechanism to overcome the drug resistance. Here, we report that a new semisynthetic saponin analogue (AG-08) triggers necrotic cell death with unprecedented pathways. AG-08-mediated necrosis depends on enhanced global proteolysis involving calpains, cathepsins, and caspases. Moreover, AG-08 generates several alterations in lysosomal function and physiology including membrane permeabilization, redistribution toward the perinuclear area, and lastly excessive tubulation. As a consequence of lysosomal impairment, the autophagic process was abolished via AG-08 treatment. Collectively, in addition to its ability to induce necrotic cell death, which makes AG-08 a promising candidate to cope with drug resistance, its unique activity mechanisms including autophagy/lysosome impairment and enhancement of proteolysis leading a strong death capacity emphasizes its potential for anticancer drug research. © en_US
dc.description.sponsorship This project was supported by The Scientific and Technological Research Council of Turkey (TUBITAK, Project No: 118S709) as a continuation of a prior project (TUBITAK, Project No: 109S345). en_US
dc.identifier.doi 10.1021/acs.chemrestox.0c00339
dc.identifier.issn 0893-228X
dc.identifier.issn 1520-5010
dc.identifier.scopus 2-s2.0-85096203166
dc.identifier.uri https://doi.org/10.1021/acs.chemrestox.0c00339
dc.identifier.uri https://hdl.handle.net/11147/10245
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.relation.ispartof Chemical Research in Toxicology en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.title Identification of a Noncanonical Necrotic Cell Death Triggered Via Enhanced Proteolysis by a Novel Sapogenol Derivative en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Üner, Göklem
gdc.author.institutional Bedir, Erdal
gdc.bip.impulseclass C4
gdc.bip.influenceclass C5
gdc.bip.popularityclass C4
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Bioengineering en_US
gdc.description.endpage 2891 en_US
gdc.description.issue 11 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 2880 en_US
gdc.description.volume 33 en_US
gdc.description.wosquality Q2
gdc.identifier.openalex W3097024051
gdc.identifier.pmid 33136369
gdc.identifier.wos WOS:000599310100019
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.diamondjournal false
gdc.oaire.impulse 5.0
gdc.oaire.influence 2.8258587E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Cell Death
gdc.oaire.keywords Molecular Conformation
gdc.oaire.keywords Saponins
gdc.oaire.keywords Mice
gdc.oaire.keywords Necrosis
gdc.oaire.keywords [No Keyword]
gdc.oaire.keywords Chlorocebus aethiops
gdc.oaire.keywords Proteolysis
gdc.oaire.keywords Animals
gdc.oaire.keywords Humans
gdc.oaire.keywords Cells, Cultured
gdc.oaire.popularity 8.169582E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 0303 health sciences
gdc.oaire.sciencefields 03 medical and health sciences
gdc.openalex.collaboration National
gdc.openalex.fwci 1.07571523
gdc.openalex.normalizedpercentile 0.76
gdc.opencitations.count 8
gdc.plumx.crossrefcites 6
gdc.plumx.mendeley 4
gdc.plumx.pubmedcites 3
gdc.plumx.scopuscites 5
gdc.scopus.citedcount 5
gdc.wos.citedcount 4
relation.isAuthorOfPublication.latestForDiscovery 461a570d-2493-4349-b634-a876ced8cd22
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4015-8abe-a4dfe192da5e

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