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dc.contributor.authorKastinen, Meeri
dc.contributor.authorSirniö, Päivi
dc.contributor.authorElomaa, Hanna
dc.contributor.authorAhtiainen, Maarit
dc.contributor.authorVäyrynen, Sara A.
dc.contributor.authorHerzig, Karl-Heinz
dc.contributor.authorMeriläinen, Sanna
dc.contributor.authorAro, Raila
dc.contributor.authorHäivälä, Reetta
dc.contributor.authorRautio, Tero
dc.contributor.authorSaarnio, Juha
dc.contributor.authorWirta, Erkki-Ville
dc.contributor.authorHelminen, Olli
dc.contributor.authorSeppälä, Toni T.
dc.contributor.authorKuopio, Teijo
dc.contributor.authorBöhm, Jan
dc.contributor.authorTuomisto, Anne
dc.contributor.authorMecklin, Jukka-Pekka
dc.contributor.authorMäkinen, Markus J.
dc.contributor.authorVäyrynen, Juha P.
dc.date.accessioned2023-04-14T11:02:33Z
dc.date.available2023-04-14T11:02:33Z
dc.date.issued2023
dc.identifier.citationKastinen, M., Sirniö, P., Elomaa, H., Ahtiainen, M., Väyrynen, S. A., Herzig, K.-H., Meriläinen, S., Aro, R., Häivälä, R., Rautio, T., Saarnio, J., Wirta, E.-V., Helminen, O., Seppälä, T. T., Kuopio, T., Böhm, J., Tuomisto, A., Mecklin, J.-P., Mäkinen, M. J., & Väyrynen, J. P. (2023). Immunological and prognostic significance of tumour necrosis in colorectal cancer. <i>British Journal of Cancer</i>, <i>128</i>(12), 2218-2226. <a href="https://doi.org/10.1038/s41416-023-02258-2" target="_blank">https://doi.org/10.1038/s41416-023-02258-2</a>
dc.identifier.otherCONVID_182700447
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/86353
dc.description.abstractBackground Colorectal cancer (CRC) causes the second most cancer deaths worldwide, but the disease course varies according to tumour characteristics and immunological factors. Our objective was to examine the associations of tumour necrosis with tumour characteristics, immune cell infiltrates, serum cytokine concentrations, as well as prognosis in CRC. Methods Three independent CRC cohorts, including 1413 patients, were analysed. Associations of the areal percentage of tumour necrosis with clinicopathologic parameters, tumour infiltrating immune cells, cytokine concentrations in systemic and mesenteric vein blood, and survival were examined. Results Higher tumour necrosis percentage associated with shorter colorectal cancer-specific survival independent of tumour grade, T, N or M-class, mismatch repair status, BRAF status, and other possible confounding factors. In the largest cohort (N = 1100), the HR for high tumour necrosis percentage (≥40% vs. <3%) was 3.22 (95% CI 1.68–6.17, Ptrend < 0.0001). Tumour necrosis percentage positively correlated with peripheral serum levels of CXCL8, a proinflammatory chemokine, and negatively correlated with mesenteric serum levels of CXCL10 and mast cell densities in the invasive margin of the tumour. Conclusions Our results support the value of tumour necrosis as a prognostic factor in colorectal cancer. CXCL8 may have a role in the systemic effects of tumour necrosis.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.ispartofseriesBritish Journal of Cancer
dc.rightsCC BY 4.0
dc.subject.othercancer microenvironment
dc.subject.othercolorectal cancer
dc.subject.othertumour biomarkers
dc.titleImmunological and prognostic significance of tumour necrosis in colorectal cancer
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202304142479
dc.contributor.laitosMatemaattis-luonnontieteellinen tiedekuntafi
dc.contributor.laitosBio- ja ympäristötieteiden laitosfi
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosFaculty of Mathematics and Scienceen
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.pagerange2218-2226
dc.relation.issn0007-0920
dc.relation.numberinseries12
dc.relation.volume128
dc.type.versionpublishedVersion
dc.rights.copyright© 2023 the Authors
dc.rights.accesslevelopenAccessfi
dc.subject.ysosyöpätaudit
dc.subject.ysobiomarkkerit
dc.subject.ysokasvaimet
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p678
jyx.subject.urihttp://www.yso.fi/onto/yso/p12288
jyx.subject.urihttp://www.yso.fi/onto/yso/p2299
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1038/s41416-023-02258-2
jyx.fundinginformationThis study was funded by Cancer Foundation Finland (59-5619 to JPV). Open Access funding provided by University of Oulu including Oulu University Hospital.
dc.type.okmA1


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