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dc.contributor.authorBerle, Magnus
dc.contributor.authorHestetun, Kjersti Elvestad
dc.contributor.authorVethe, Heidrun
dc.contributor.authorChera, Simona
dc.contributor.authorPaulo, Joao A.
dc.contributor.authorDahl, Olav
dc.contributor.authorMyklebust, Mette Pernille
dc.date.accessioned2023-01-31T13:34:35Z
dc.date.available2023-01-31T13:34:35Z
dc.date.created2022-05-20T14:42:41Z
dc.date.issued2022
dc.identifier.issn1109-6535
dc.identifier.urihttps://hdl.handle.net/11250/3047463
dc.description.abstractBackground/Aim: Better stratification of the risk of relapse will help select the right patients for adjuvant treatment and improve targeted therapies for patients with colon cancer. Materials and Methods: To understand why a subset of tumors relapse, we compared the proteome of two groups of patients with colon cancer with similar stage, stratified based on the presence or absence of recurrence. Results: Using tumor biopsies from the primary operation, we identified dissimilarity between recurrent and nonrecurrent mismatch satellite stable colon cancer and found that signaling related to immune activation and inflammation was associated with relapse. Conclusion: Immune modulation may have an effect on mismatch satellite stable colon cancer. At present, immune therapy is offered primarily to microsatellite instable colon cancer. Hopefully, immune therapy in mismatch satellite stable colon cancer beyond PD-1 and PD-L1 inhibitors can be implemented.en_US
dc.language.isoengen_US
dc.publisherInternational Institute of Anticancer Researchen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleMapping Proteome Changes in Microsatellite Stable, Recurrent Colon Cancer Reveals a Significant Immune System Signatureen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.21873/cgp.20309
dc.identifier.cristin2026013
dc.source.journalCancer Genomics & Proteomicsen_US
dc.source.pagenumber130-144en_US
dc.relation.projectNorges forskningsråd: 251041en_US
dc.relation.projectNovo Nordisk Fonden: NNF15OC0015054en_US
dc.relation.projectNovo Nordisk Fonden: NNF21OC0067325en_US
dc.relation.projectNorges forskningsråd: 304615en_US
dc.identifier.citationCancer Genomics & Proteomics. 2022, 19 (2), 130-144.en_US
dc.source.volume19en_US
dc.source.issue2en_US


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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