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dc.contributor.authorKarjula, Topias
dc.contributor.authorElomaa, Hanna
dc.contributor.authorVäyrynen, Sara A.
dc.contributor.authorKuopio, Teijo
dc.contributor.authorAhtiainen, Maarit
dc.contributor.authorMustonen, Olli
dc.contributor.authorPuro, Iiris
dc.contributor.authorNiskakangas, Anne
dc.contributor.authorMecklin, Jukka-Pekka
dc.contributor.authorBöhm, Jan
dc.contributor.authorWirta, Erkki-Ville
dc.contributor.authorSeppälä, Toni T.
dc.contributor.authorSihvo, Eero
dc.contributor.authorYannopoulos, Fredrik
dc.contributor.authorHelminen, Olli
dc.contributor.authorVäyrynen, Juha P.
dc.date.accessioned2024-03-05T07:42:05Z
dc.date.available2024-03-05T07:42:05Z
dc.date.issued2024
dc.identifier.citationKarjula, T., Elomaa, H., Väyrynen, S. A., Kuopio, T., Ahtiainen, M., Mustonen, O., Puro, I., Niskakangas, A., Mecklin, J.-P., Böhm, J., Wirta, E.-V., Seppälä, T. T., Sihvo, E., Yannopoulos, F., Helminen, O., & Väyrynen, J. P. (2024). Multiplexed analysis of macrophage polarisation in pulmonary metastases of microsatellite stable colorectal cancer. <i>Cancer Immunology, Immunotherapy</i>, <i>73</i>, Article 59. <a href="https://doi.org/10.1007/s00262-024-03646-0" target="_blank">https://doi.org/10.1007/s00262-024-03646-0</a>
dc.identifier.otherCONVID_207402408
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/93802
dc.description.abstractTumour-associated macrophages (TAMs) express a continuum of phenotypes ranging from an anti-tumoural M1-like phenotype to a pro-tumoural M2-like phenotype. During cancer progression, TAMs may shift to a more M2-like polarisation state, but the role of TAMs in CRC metastases is unclear. We conducted a comprehensive spatial and prognostic analysis of TAMs in CRC pulmonary metastases and corresponding primary tumours using multiplexed immunohistochemistry and machine learning-based image analysis. We obtained data from 106 resected pulmonary metastases and 74 corresponding primary tumours. TAMs in the resected pulmonary metastases were located closer to the cancer cells and presented a more M2-like polarised state in comparison to the primary tumours. Higher stromal M2-like macrophage densities in the invasive margin of pulmonary metastases were associated with worse 5-year overall survival (HR 3.19, 95% CI 1.35–7.55, p = 0.008). The results of this study highlight the value of multiplexed analysis of macrophage polarisation in cancer metastases and might have clinical implications in future cancer therapy.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofseriesCancer Immunology, Immunotherapy
dc.rightsCC BY 4.0
dc.subject.otherPulmonary metastases
dc.subject.othercolorectal cancer
dc.subject.othertumour-associated macrophages
dc.subject.othermacrophage polarisation
dc.subject.othercancer immunology
dc.titleMultiplexed analysis of macrophage polarisation in pulmonary metastases of microsatellite stable colorectal cancer
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202403052269
dc.contributor.laitosBio- ja ympäristötieteiden laitosfi
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosMatemaattis-luonnontieteellinen tiedekuntafi
dc.contributor.laitosDepartment of Biological and Environmental Scienceen
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.contributor.laitosFaculty of Mathematics and Scienceen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn0340-7004
dc.relation.volume73
dc.type.versionpublishedVersion
dc.rights.copyright© The Author(s) 2024
dc.rights.accesslevelopenAccessfi
dc.subject.ysomakrofagit
dc.subject.ysosuolistosyövät
dc.subject.ysoimmunologia
dc.subject.ysoetäpesäkkeet
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p27579
jyx.subject.urihttp://www.yso.fi/onto/yso/p25845
jyx.subject.urihttp://www.yso.fi/onto/yso/p18810
jyx.subject.urihttp://www.yso.fi/onto/yso/p2298
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1007/s00262-024-03646-0
jyx.fundinginformationOpen Access funding provided by University of Oulu (including Oulu University Hospital). This study was funded by Instrumentarium Science Foundation (O.H), Mary and Georg C. Ehrnrooth Foundation (O.H), Finnish State Research Funding (O.H, J-P.M), Cancer Foundation Finland (J.P.V), Sigrid Jusélius Foundation (J.P.V), and J&A Erkko Foundation (J-P.M, T.T.S).
dc.type.okmA1


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