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dc.contributor.authorJunttila, Anna
dc.contributor.authorHelminen, Olli
dc.contributor.authorVäyrynen, Juha P.
dc.contributor.authorAhtiainen, Maarit
dc.contributor.authorKenessey, Istvan
dc.contributor.authorJalkanen, Sirpa
dc.contributor.authorMecklin, Jukka-Pekka
dc.contributor.authorKellokumpu, Ilmo
dc.contributor.authorKuopio, Teijo
dc.contributor.authorBöhm, Jan
dc.contributor.authorMrena, Johanna
dc.date.accessioned2021-09-27T10:08:13Z
dc.date.available2021-09-27T10:08:13Z
dc.date.issued2020
dc.identifier.citationJunttila, A., Helminen, O., Väyrynen, J. P., Ahtiainen, M., Kenessey, I., Jalkanen, S., Mecklin, J.-P., Kellokumpu, I., Kuopio, T., Böhm, J., & Mrena, J. (2020). Immunophenotype based on inflammatory cells, PD-1/PD-L1 signalling pathway and M2 macrophages predicts survival in gastric cancer. <i>British Journal of Cancer</i>, <i>123</i>(11), 1625-1632. <a href="https://doi.org/10.1038/s41416-020-01053-7" target="_blank">https://doi.org/10.1038/s41416-020-01053-7</a>
dc.identifier.otherCONVID_42417111
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/77920
dc.description.abstractBackground: Immune response against cancer has prognostic impact but its role in gastric cancer is poorly known. The aim of the study was to assess the prognostic significance of immune cell score (CD3+, CD8+), tumour immune escape (PD-L1, PD-1) and immune tolerance (Clever-1). Methods: After exclusion of Epstein-Barr virus positive (n = 4) and microsatellite instable (n = 6) tumours, the study included 122 patients with GC undergoing D2 gastrectomy. CD3+ and CD8+ based ICS, PD-L1, PD-1 and Clever-1 expressions were evaluated. Differences in survival were examined using Cox regression adjusted for confounders. The primary outcome was 5-year survival. Results: The 5-year overall survival rate was 43.4%. High ICS was associated with improved overall survival (adjusted HR 0.48 (95% CI 0.26-0.87)) compared to low ICS. In the high ICS group, patients with PD-L1 expression (5-year survival 69.2 vs. 53.1%, p = 0.317), high PD-1 (5-year survival 70.6 vs. 55.3% p = 0.312) and high Clever-1 (5-year survival 72.0% vs. 45.5% (p = 0.070) had poor prognosis. Conclusions: High ICS was associated with improved survival. In the high ICS group, patients with high PD-L1, PD-1 and Clever-1 had poor prognosis highlighting the importance of immune escape and immune tolerance in GC.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.ispartofseriesBritish Journal of Cancer
dc.rightsCC BY 4.0
dc.titleImmunophenotype based on inflammatory cells, PD-1/PD-L1 signalling pathway and M2 macrophages predicts survival in gastric cancer
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202109274988
dc.contributor.laitosBio- ja ympäristötieteiden laitosfi
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosDepartment of Biological and Environmental Scienceen
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.contributor.oppiaineSolu- ja molekyylibiologiafi
dc.contributor.oppiaineCell and Molecular Biologyen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange1625-1632
dc.relation.issn0007-0920
dc.relation.numberinseries11
dc.relation.volume123
dc.type.versionpublishedVersion
dc.rights.copyright© The Author(s), under exclusive licence to Cancer Research UK 2020
dc.rights.accesslevelopenAccessfi
dc.subject.ysoennusteet
dc.subject.ysosyöpätaudit
dc.subject.ysoimmuunivaste
dc.subject.ysomahasyöpä
dc.subject.ysofenotyyppi
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p3297
jyx.subject.urihttp://www.yso.fi/onto/yso/p678
jyx.subject.urihttp://www.yso.fi/onto/yso/p21599
jyx.subject.urihttp://www.yso.fi/onto/yso/p6111
jyx.subject.urihttp://www.yso.fi/onto/yso/p13074
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1038/s41416-020-01053-7
jyx.fundinginformationThis study was funded by the Finnish State Research Funding (O.H.), the Instrumentarium Science Foundation (O.H.) and the Mary and Georg C. Ehrnrooth Foundation (O.H.).
dc.type.okmA1


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