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dc.contributor.authorWang, Ruoxi W.
dc.contributor.authorViganò, Sonia
dc.contributor.authorBen-David, Uri
dc.contributor.authorAmon, Angelika
dc.contributor.authorSantaguida, Stefano
dc.date.accessioned2024-11-07T15:22:09Z
dc.date.available2024-11-07T15:22:09Z
dc.date.issued2021-06-08
dc.identifier.urihttps://hdl.handle.net/1721.1/157501
dc.description.abstractThe immune system plays a major role in the protection against cancer. Identifying and characterizing the pathways mediating this immune surveillance are thus critical for understanding how cancer cells are recognized and eliminated. Aneuploidy is a hallmark of cancer, and we previously found that untransformed cells that had undergone senescence due to highly abnormal karyotypes are eliminated by natural killer (NK) cells in vitro. However, the mechanisms underlying this process remained elusive. Here, using an in vitro NK cell killing system, we show that non‐cell‐autonomous mechanisms in aneuploid cells predominantly mediate their clearance by NK cells. Our data indicate that in untransformed aneuploid cells, NF‐κB signaling upregulation is central to elicit this immune response. Inactivating NF‐κB abolishes NK cell‐mediated clearance of untransformed aneuploid cells. In cancer cell lines, NF‐κB upregulation also correlates with the degree of aneuploidy. However, such upregulation in cancer cells is not sufficient to trigger NK cell‐mediated clearance, suggesting that additional mechanisms might be at play during cancer evolution to counteract NF‐κB‐mediated immunogenicity.en_US
dc.publisherNature Publishing Group UKen_US
dc.relation.isversionofhttps://doi.org/10.15252/embr.202052032en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNature Publishing Group UKen_US
dc.titleAneuploid senescent cells activate NF-κB to promote their immune clearance by NK cellsen_US
dc.typeArticleen_US
dc.identifier.citationThe EMBO Reports. 2021 Jun 08;22(8):EMBR202052032en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentHoward Hughes Medical Instituteen_US
dc.relation.journalEmbo Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2024-10-27T17:21:54Z
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dspace.date.submission2024-10-27T17:21:54Z
mit.journal.volume22en_US
mit.journal.issue8en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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