Investigation of CCL18 and A1AT as potential urinary biomarkers for bladder cancer detection

dc.contributor.authorMiyake, Makito
dc.contributor.authorRoss, Shanti
dc.contributor.authorLawton, Adrienne
dc.contributor.authorChang, Myron
dc.contributor.authorDai, Yunfeng
dc.contributor.authorMengual Brichs, Lourdes
dc.contributor.authorAlcaraz Asensio, Antonio
dc.contributor.authorGiacoia, Eva Gomes
dc.contributor.authorGoodison, Steve
dc.contributor.authorRosser, Charles J.
dc.date.accessioned2015-01-12T08:53:06Z
dc.date.available2015-01-12T08:53:06Z
dc.date.issued2013-09-05
dc.date.updated2015-01-12T08:53:06Z
dc.description.abstractBACKGROUND: In this study, we further investigated the association of two biomarkers, CCL18 and A1AT, with bladder cancer (BCa) and evaluated the influence of potentially confounding factors in an experimental model. METHODS: In a cohort of 308 subjects (102 with BCa), urinary concentrations of CCL18 and A1AT were assessed by enzyme-linked immunosorbent assay (ELISA). In an experimental model, benign or cancerous cells, in addition to blood, were added to urines from healthy controls and analyzed by ELISA. Lastly, immunohistochemical staining for CCL18 and A1AT in human bladder tumors was performed. RESULTS: Median urinary protein concentrations of CCL18 (52.84 pg/ml vs. 11.13 pg/ml, p < 0.0001) and A1AT (606.4 ng/ml vs. 120.0 ng/ml, p < 0.0001) were significantly elevated in BCa subjects compared to controls. Furthermore, the addition of whole blood to pooled normal urine resulted in a significant increase in both CCL18 and A1AT. IHC staining of bladder tumors revealed CCL18 immunoreactivity in inflammatory cells only, and there was no significant increase in these immunoreactive cells within benign and cancerous tissue and no association with BCa grade nor stage was noted. A1AT immunoreactivity was observed in the cytoplasm of epithelia cells and intensity of immunostaining increased with tumor grade, but not tumor stage. CONCLUSIONS: Further development of A1AT as a diagnostic biomarker for BCa is warranted.
dc.format.extent10 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec637783
dc.identifier.issn1471-2490
dc.identifier.pmid24011266
dc.identifier.urihttps://hdl.handle.net/2445/61144
dc.language.isoeng
dc.publisherBioMed Central
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.1186/1471-2490-13-42
dc.relation.ispartofBMC Urology , 2013, vol. 13, num. 1, p. 42
dc.relation.urihttp://dx.doi.org/10.1186/1471-2490-13-42
dc.rightscc-by (c) Miyake, M. et al., 2013
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Ciències Fisiològiques)
dc.subject.classificationCàncer de bufeta
dc.subject.classificationMarcadors tumorals
dc.subject.classificationAssaigs clínics
dc.subject.classificationOrina
dc.subject.otherBladder cancer
dc.subject.otherTumor markers
dc.subject.otherClinical trials
dc.subject.otherUrine
dc.titleInvestigation of CCL18 and A1AT as potential urinary biomarkers for bladder cancer detection
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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