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dc.contributor.authorTahkola, Kyösti
dc.contributor.authorAhtiainen, Maarit
dc.contributor.authorKellokumpu, Ilmo
dc.contributor.authorMecklin, Jukka-Pekka
dc.contributor.authorLaukkarinen Johanna
dc.contributor.authorLaakkonen, Joni
dc.contributor.authorKenessey, Istvan
dc.contributor.authorJalkanen, Sirpa
dc.contributor.authorSalmi, Marko
dc.contributor.authorBöhm, Jan
dc.date.accessioned2020-07-21T08:51:38Z
dc.date.available2020-07-21T08:51:38Z
dc.date.issued2021
dc.identifier.citationTahkola, Kyösti, Ahtiainen, Maarit, Kellokumpu, Ilmo, Mecklin, Jukka-Pekka, Laukkarinen Johanna, Laakkonen, Joni, Kenessey, Istvan, Jalkanen, Sirpa, Salmi, Marko, Böhm, Jan. (2021). Prognostic impact of CD73 expression and its relationship to PD-L1 in patients with radically treated pancreatic cancer. <i>Virchows Archiv</i>, <i>478</i>(2), 209-217. <a href="https://doi.org/10.1007/s00428-020-02888-4" target="_blank">https://doi.org/10.1007/s00428-020-02888-4</a>
dc.identifier.otherCONVID_41613261
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/71213
dc.description.abstractImmune suppressing molecule CD73 is overexpressed in various cancers and associated with poor survival. Little is so far known about the predictive value of CD73 in pancreatic ductal adenocarcinoma (PDAC). The purpose of this study was to investigate the prognostic significance of CD73 in PDAC. The study material consisted of 110 radically treated patients for PDAC. Tissue microarray blocks were constructed and stained immunohistochemically using CD73 antibody. Staining intensity and numbers of stained tumour cells, inflammatory cells, stroma, and blood vessels were assessed. High-level CD73 expression in tumour cells was positively associated with PD-L1 expression, perineural invasion, and histopathological grade. CD73 positivity in tumour-infiltrating lymphocytes was significantly associated with lymph node metastasis. Lymphocytic CD73 positivity was also associated with staining positivity in both stroma and vascular structures. In addition, CD73 positivity in vascular structures and stroma were associated with each other. There were no significant associations between CD73 positive tumour cells and CD73 positivity in any other cell types. PD-L1 expression was associated with CD73 staining positivity in stroma (p = 0.007) and also with histopathological grade (p = 0.033) and T class (p = 0.016) of the primary tumour. CD73 positivity in tumour cells was significantly associated with poor disease-specific (p = 0.021) and overall survival (p = 0.016). In multivariate analysis, CD73 positivity in tumour cells was an independent negative prognostic factor together with histopathological grade, TNM stage, and low immune cell score. In conclusion, high CD73 expression in tumour cells is associated with poor survival in PDAC independently of the number of tumour-infiltrating lymphocytes or TNM stage.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofseriesVirchows Archiv
dc.rightsCC BY 4.0
dc.subject.otherpancreatic cancer
dc.subject.othermicroenvironment
dc.subject.otherCD73
dc.subject.otherPD-L1
dc.subject.otherprognosis
dc.titlePrognostic impact of CD73 expression and its relationship to PD-L1 in patients with radically treated pancreatic cancer
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202007215367
dc.contributor.laitosLiikuntatieteellinen tiedekuntafi
dc.contributor.laitosFaculty of Sport and Health Sciencesen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange209-217
dc.relation.issn0945-6317
dc.relation.numberinseries2
dc.relation.volume478
dc.type.versionpublishedVersion
dc.rights.copyright© 2020 the Author(s)
dc.rights.accesslevelopenAccessfi
dc.subject.ysoimmuunijärjestelmä
dc.subject.ysohaimasyöpä
dc.subject.ysoentsyymit
dc.subject.ysosyöpäsolut
dc.subject.ysoennusteet
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p16041
jyx.subject.urihttp://www.yso.fi/onto/yso/p20163
jyx.subject.urihttp://www.yso.fi/onto/yso/p4769
jyx.subject.urihttp://www.yso.fi/onto/yso/p23898
jyx.subject.urihttp://www.yso.fi/onto/yso/p3297
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1007/s00428-020-02888-4
jyx.fundinginformationThis study received funding from the Finnish Cancer Foundation, the Jane and Aatos Erkko Foundation and the State Research Funding.
dc.type.okmA1


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