Soluble triggering receptor expressed on myeloid cells 1 in lung cancer

dc.contributor.authorKuemmel, Andreas
dc.contributor.authorAlflen, Astrid
dc.contributor.authorSchmidt, Lars Henning
dc.contributor.authorSebastian, Martin
dc.contributor.authorWiewrodt, Rainer
dc.contributor.authorSchulze, Arik Bernard
dc.contributor.authorBuhl, Roland
dc.contributor.authorRadsak, Markus
dc.date.accessioned2018-12-19T12:30:04Z
dc.date.available2018-12-19T13:30:04Z
dc.date.issued2018
dc.description.abstractSoluble Triggering Receptor Expressed on Myeloid Cells 1 (sTREM-1) can be found in the sera of patients with infectious, autoimmune and malignant diseases. The primary objective of this study was to investigate the prognostic significance of sTREM-1 in lung cancer patients. We analyzed the sera of 164 patients with lung cancer of all histologies and all stages at the time of diagnosis. We employed an ELISA using the anti-TREM-1 clone 6B1.1G12 mAb and recombinant human TREM-1. Patient data was collected retrospectively by chart review. In ROC-analysis, a sTREM-1 serum level of 163.1  pg/ml showed the highest Youden-Index. At this cut-off value sTREM-1 was a marker of short survival in patients with NSCLC (median survival 8.5 vs. 13.3 months, p = 0.04). A Cox regression model showed stage (p < 0.001) and sTREM-1 (p = 0.011) to indicate short survival. There were no differences in sTREM-1 serum values among patients with or without infection, pleural effusion or COPD. sTREM-1 was not associated with metastasis at the time of diagnosis and was not a predictor of subsequent metastasis. In SCLC patients sTREM-1 levels were lower than in NSCLC patients (p = 0.001) and did not predict survival. sTREM-1 did not correlate with CRP or the number of neutrophils. In non-small cell lung cancer patients, sTREM-1 in serum has prognostic significance.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizin
dc.identifier.doihttp://doi.org/10.25358/openscience-252
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/254
dc.language.isoeng
dc.rightsCC-BY-4.0de_DE
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleSoluble triggering receptor expressed on myeloid cells 1 in lung canceren_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.journal.titleScientific reports
jgu.journal.volume8
jgu.organisation.departmentFB 04 Medizin
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternativeArt. 10766
jgu.publisher.doi10.1038/s41598-018-28971-0
jgu.publisher.issn2045-2322
jgu.publisher.nameMacmillan Publishers Limited, part of Springer Nature
jgu.publisher.placeLondon
jgu.publisher.urihttp://dx.doi.org/10.1038/s41598-018-28971-0
jgu.publisher.year2018
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode610
jgu.type.dinitypeArticle
jgu.type.resourceText
jgu.type.versionPublished versionen_GB
opus.affiliatedBuhl, Roland
opus.affiliatedRadsak, Markus
opus.date.accessioned2018-12-19T12:30:04Z
opus.date.available2018-12-19T13:30:04
opus.date.modified2019-01-10T10:23:24Z
opus.identifier.opusid58708
opus.institute.number0412
opus.institute.number0427
opus.metadataonlyfalse
opus.organisation.stringFB 04: Medizin: Institut für Immunologiede_DE
opus.organisation.stringFB 04: Medizin: III. Medizinische Klinik und Poliklinikde_DE
opus.subject.dfgcode00-000
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_GB

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