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dc.contributor.authorIanevski, Aleksandr
dc.contributor.authorKulesskiy, Evgeny
dc.contributor.authorKrpina, Klara
dc.contributor.authorLou, Guofeng
dc.contributor.authorAman, Yahyah
dc.contributor.authorBugai, Andrii
dc.contributor.authorAasumets, Koit
dc.contributor.authorAkimov, Yevhen
dc.contributor.authorBulanova, Daria
dc.contributor.authorGildemann, Kiira
dc.contributor.authorArutyunyan, Albert F.
dc.contributor.authorSusova, Olga Yu.
dc.contributor.authorZhuze, Alexei L.
dc.contributor.authorJi, Ping
dc.contributor.authorWang, Wei
dc.contributor.authorHolien, Toril
dc.contributor.authorBugge, Marit
dc.contributor.authorZusinaite, Eva
dc.contributor.authorOksenych, Valentyn
dc.contributor.authorLysvand, Hilde
dc.contributor.authorGerhold, Joachim M.
dc.contributor.authorBjørås, Magnar
dc.contributor.authorJohansen, Pål
dc.contributor.authorWaage, Anders
dc.contributor.authorHeckman, Caroline A.
dc.contributor.authorFang, Evandro Fei
dc.contributor.authorKainov, Denis
dc.date.accessioned2021-02-08T09:38:01Z
dc.date.available2021-02-08T09:38:01Z
dc.date.created2020-07-22T14:32:31Z
dc.date.issued2020
dc.identifier.citationCancers. 2020, 12 (6), 1-19.en_US
dc.identifier.issn2072-6694
dc.identifier.urihttps://hdl.handle.net/11250/2726557
dc.description.abstractBackground: The evidence that pan-Bcl-2 or Bcl-xL-specific inhibitors prematurely kill virus-infected or RNA/DNA-transfected cells provides rationale for investigating these apoptotic inducers further. We hypothesized that not only invasive RNA or DNA (biological factors) but also DNA/RNA-damaging chemical or physical factors could trigger apoptosis that have been sensitized with pan-Bcl-2 or Bcl-xL-specific agents; Methods: We tested chemical and physical factors plus Bcl-xL-specific inhibitor A-1155463 in cells of various origins and the small roundworms (C. elegans); Results: We show that combination of a A-1155463 along with a DNA-damaging agent, 4-nitroquinoline-1-oxide (4NQO), prematurely kills cells of various origins as well as C. elegans. The synergistic effect is p53-dependent and associated with the release of Bad and Bax from Bcl-xL, which trigger mitochondrial outer membrane permeabilization. Furthermore, we found that combining Bcl-xL-specific inhibitors with various chemical compounds or physical insults also induced cell death; Conclusions: Thus, we were able to identify several biological, chemical and physical triggers of the evolutionarily conserved Bcl-xL-mediated apoptotic pathway, shedding light on strategies and targets for novel drug development.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleChemical, Physical and Biological Triggers of Evolutionary Sonserved Bcl-xL-Mediated Apoptosisen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber1-19en_US
dc.source.volume12en_US
dc.source.journalCancersen_US
dc.source.issue6en_US
dc.identifier.doi10.3390/cancers12061694
dc.identifier.cristin1820197
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal