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Increased Production of the Soluble Tumor-Associated Antigens CA19-9, CA125, and CA15-3 in Rheumatoid Arthritis

dc.contributor.authorSzekanecz, Évaen_US
dc.contributor.authorSándor, Zsuzsaen_US
dc.contributor.authorAntal-Szalmás, Péteren_US
dc.contributor.authorSoós, Lillaen_US
dc.contributor.authorLakos, Gabriellaen_US
dc.contributor.authorBesenyei, Timeaen_US
dc.contributor.authorSzentpétery, Ágnesen_US
dc.contributor.authorSimkovics, Eniköen_US
dc.contributor.authorSzántó, Jánosen_US
dc.contributor.authorKiss, Emeseen_US
dc.contributor.authorKoch, Alisa E.en_US
dc.contributor.authorSzekanecz, Zoltánen_US
dc.date.accessioned2010-06-01T20:05:56Z
dc.date.available2010-06-01T20:05:56Z
dc.date.issued2007-06en_US
dc.identifier.citationSZEKANECZ, ÉVA; SÁNDOR, ZSUZSA; ANTAL-SZALMÁS, PÉTER; SOÓS, LILLA; LAKOS, GABRIELLA; BESENYEI, TIMEA; SZENTPÉTERY, ÁGNES; SIMKOVICS, ENIKÖ; SZÁNTÓ, JÁNOS; KISS, EMESE; KOCH, ALISA E.; SZEKANECZ, ZOLTÁN (2007). "Increased Production of the Soluble Tumor-Associated Antigens CA19-9, CA125, and CA15-3 in Rheumatoid Arthritis." Annals of the New York Academy of Sciences 1108(1 Autoimmunity, Part D: Autoimmune Disease, Annus Mirabilis ): 359-371. <http://hdl.handle.net/2027.42/73224>en_US
dc.identifier.issn0077-8923en_US
dc.identifier.issn1749-6632en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/73224
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=17893999&dopt=citationen_US
dc.description.abstractSome tumor-associated antigens (TAAs) are expressed on inflammatory cells. We previously detected carcinoembryonic antigen (CEA; CD66) in the rheumatoid (RA) synovium. The production of CEA, CA19-9, CA125, and CA15.3, may be increased in patients with RA, scleroderma, lupus, and SjÖgren's syndrome (SS). Some of these TAAs contain sialylated carbohydrate motifs and they are involved in tumor-associated cell adhesion and metastasis. We assessed levels of TAAs in the sera of RA patients and healthy subjects. Serum TAA levels were correlated with disease markers including serum rheumatoid factor (RF), C-reactive protein (CRP), and anti-CCP antibody levels, DAS28, age disease duration. TAAs including CEA, CA15-3, CA72-4, CA125, and CA19-9, and neuron-specific enolase (NSE) were assessed by immunoassay in the sera of 75 patients with RA and 50 age- and sex-matched healthy controls. Normal upper limits for these TAAs were 3.4 Μg/L, 25 kU/L, 6.9 kU/L, 35 kU/L, 34 kU/L, and 16.3 Μg/L, respectively. There were significantly more RA patients showing abnormally high levels of CA125 (10.8% versus 7.1%), CA19-9 (8.1% versus 0%), and CA15-3 (17.6% versus 14.3%) in comparison to controls ( P < 0.05). The mean absolute serum levels of CA125 (23.9 ± 1.8 versus 16.8 ± 2.2 kU/L) and CA19-9 (14.2 ± 1.2 versus 10.5 ± 1.6 kU/L) were also significantly higher in RA compared to controls ( P < 0.05). Among RA patients, serum CEA showed significant correlation with RF ( r = 0.270; P < 0.05). None of the assessed TAAs showed any correlation with CRP, anti-CCP, DAS28, age or disease duration. The concentration of some TAAs may be elevated in the sera of patients with established RA in comparison to healthy subjects. CEA, CA19-9, CA125, and CA15-3 contain carbohydrate motifs and thus they may be involved in synovitis-associated adhesive events. Furthermore, some TAAs, such as CEA, may also correlate with prognostic factors, such as serum RF levels.en_US
dc.format.extent203699 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Incen_US
dc.rights2007 New York Academy of Sciencesen_US
dc.subject.otherRheumatoid Arthritisen_US
dc.subject.otherTumor Antigensen_US
dc.subject.otherAnti-CCP Antibodyen_US
dc.subject.otherRheumatoid Factoren_US
dc.subject.otherCarcinoembryonic Antigenen_US
dc.titleIncreased Production of the Soluble Tumor-Associated Antigens CA19-9, CA125, and CA15-3 in Rheumatoid Arthritisen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelScience (General)en_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan Health System, Department of Internal Medicine, Division of Rheumatology, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherDepartment of Oncology, University of Debrecen Medical and Health Science Center, Debrecen, Hungaryen_US
dc.contributor.affiliationotherRheumatology Division, University of Debrecen Medical and Health Science Center, Debrecen, Hungaryen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Debrecen Medical and Health Science Center, Debrecen, Hungaryen_US
dc.contributor.affiliationotherDepartment of Clinical Biochemistry and Molecular Pathology, Third Department of Medicine, University of Debrecen Medical and Health Science Center, Debrecen, Hungaryen_US
dc.contributor.affiliationotherLaboratory of Immunology, University of Debrecen Medical and Health Science Center, Debrecen, Hungaryen_US
dc.identifier.pmid17893999en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/73224/1/annals.1422.037.pdf
dc.identifier.doi10.1196/annals.1422.037en_US
dc.identifier.sourceAnnals of the New York Academy of Sciencesen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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