Spectrally separated dual-label upconversion luminescence lateral flow assay for cancer-specific STn-glycosylation in CA125 and CA15-3

dc.contributor.authorEkman Miikka
dc.contributor.authorSalminen Teppo
dc.contributor.authorRaiko Kirsti
dc.contributor.authorSoukka Tero
dc.contributor.authorGidwani Kamlesh
dc.contributor.authorMartiskainen Iida
dc.contributor.organizationfi=InFLAMES Lippulaiva|en=InFLAMES Flagship|
dc.contributor.organizationfi=biotekniikka|en=Biotechnology|
dc.contributor.organization-code1.2.246.10.2458963.20.98373201676
dc.contributor.organization-code2607051
dc.contributor.organization-code2610102
dc.converis.publication-id387617668
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/387617668
dc.date.accessioned2025-08-28T00:34:13Z
dc.date.available2025-08-28T00:34:13Z
dc.description.abstractMultiplexed lateral flow assays (LFAs) offer efficient on-site testing by simultaneously detecting multiple biomarkers from a single sample, reducing costs. In cancer diagnostics, where biomarkers can lack specificity, multiparameter detection provides more information at the point-of-care. Our research focuses on epithelial ovarian cancer (EOC), where STn-glycosylated forms of CA125 and CA15-3 antigens can better discriminate cancer from benign conditions. We have developed a dual-label LFA that detects both CA125-STn and CA15-3-STn within a single anti-STn antibody test line. This utilizes spectral separation of green (540 nm) and blue (450 nm) emitting erbium (NaYF<sub>4</sub>:Yb<sup>3+</sup>, Er<sup>3+</sup>)- and thulium (NaYF<sub>4</sub>: Yb<sup>3+</sup>, Tm<sup>3+</sup>)-doped upconverting nanoparticle (UCNP) reporters conjugated with antibodies against the protein epitopes in CA125 or CA15-3. This technology allows the simultaneous detection of different antigen variants from a single test line. The developed proof-of-concept dual-label LFA was able to distinguish between the ascites fluid samples from diagnosed ovarian cancer patients (n = 10) and liver cirrhosis ascites fluid samples (n = 3) used as a negative control. The analytical sensitivity of CA125-STn for the dual-label LFA was 1.8 U/ml in buffer and 3.6 U/ml in ascites fluid matrix. Here we demonstrate a novel approach of spectrally separated measurement of STn-glycosylated forms of two different cancer-associated protein biomarkers by using UCNP reporter technology.
dc.format.pagerange3251
dc.format.pagerange3260
dc.identifier.eissn1618-2650
dc.identifier.jour-issn1618-2642
dc.identifier.olddbid205961
dc.identifier.oldhandle10024/188988
dc.identifier.urihttps://www.utupub.fi/handle/11111/38088
dc.identifier.urlhttps://link.springer.com/article/10.1007/s00216-024-05275-z
dc.identifier.urnURN:NBN:fi-fe2025082787178
dc.language.isoen
dc.okm.affiliatedauthorEkman, Miikka
dc.okm.affiliatedauthorSalminen, Teppo
dc.okm.affiliatedauthorRaiko, Kirsti
dc.okm.affiliatedauthorSoukka, Tero
dc.okm.affiliatedauthorGidwani, Kamlesh
dc.okm.affiliatedauthorMartiskainen, Iida
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSpringer Nature
dc.publisher.countryGermanyen_GB
dc.publisher.countrySaksafi_FI
dc.publisher.country-codeDE
dc.relation.doi10.1007/s00216-024-05275-z
dc.relation.ispartofjournalAnalytical and Bioanalytical Chemistry
dc.relation.issue13
dc.relation.volume416
dc.source.identifierhttps://www.utupub.fi/handle/10024/188988
dc.titleSpectrally separated dual-label upconversion luminescence lateral flow assay for cancer-specific STn-glycosylation in CA125 and CA15-3
dc.year.issued2024

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