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Detection of Biomarkers with Solid-Phase Proximity Ligation Assay in Patients with Colorectal Cancer

BACKGROUND: In the search for prognostic biomarkers, a significant amount of precious biobanked blood samples is needed for conventional analyses. Solid-phase proximity ligation assay (SP-PLA) is an analytic method with the ability to analyze many proteins at the same time in small amounts of plasma...

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Autores principales: Ghanipour, Lana, Darmanis, Spyros, Landegren, Ulf, Glimelius, Bengt, Påhlman, Lars, Birgisson, Helgi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907971/
https://www.ncbi.nlm.nih.gov/pubmed/27267845
http://dx.doi.org/10.1016/j.tranon.2016.04.001
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author Ghanipour, Lana
Darmanis, Spyros
Landegren, Ulf
Glimelius, Bengt
Påhlman, Lars
Birgisson, Helgi
author_facet Ghanipour, Lana
Darmanis, Spyros
Landegren, Ulf
Glimelius, Bengt
Påhlman, Lars
Birgisson, Helgi
author_sort Ghanipour, Lana
collection PubMed
description BACKGROUND: In the search for prognostic biomarkers, a significant amount of precious biobanked blood samples is needed for conventional analyses. Solid-phase proximity ligation assay (SP-PLA) is an analytic method with the ability to analyze many proteins at the same time in small amounts of plasma. The aim of this study was to explore the potential use of SP-PLA for biomarker validation in patients with colorectal cancer (CRC). MATERIAL AND METHODS: Plasma samples from patients with stage I to IV CRC, with (n = 31) and without (n = 29) disease dissemination at diagnosis or later, were analyzed with SP-PLA using 35 antibodies targeting an equal number of proteins in 5-μl plasma samples. Carcinoembryonic antigen (CEA), analyzed earlier in this cohort using a different technology, was used as a reference. RESULTS: A total of 21 of the 35 investigated proteins were detectable with SP-PLA. Patients in stage II to III with disseminated disease had lower plasma concentrations of HCC-4 (P = .025). Low plasma levels of tissue inhibitor of metalloproteinases–1 were seen in patients with disseminated disease stage II (P = .003). The level of CEA was higher in patients with disease dissemination compared with those without (P = .007). CONCLUSION: SP-PLA has the ability to analyze many protein markers simultaneously in a small amount of blood. However, none of the markers selected for the present SP-PLA analyses gave better prognostic information than CEA.
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spelling pubmed-49079712016-06-22 Detection of Biomarkers with Solid-Phase Proximity Ligation Assay in Patients with Colorectal Cancer Ghanipour, Lana Darmanis, Spyros Landegren, Ulf Glimelius, Bengt Påhlman, Lars Birgisson, Helgi Transl Oncol Original article BACKGROUND: In the search for prognostic biomarkers, a significant amount of precious biobanked blood samples is needed for conventional analyses. Solid-phase proximity ligation assay (SP-PLA) is an analytic method with the ability to analyze many proteins at the same time in small amounts of plasma. The aim of this study was to explore the potential use of SP-PLA for biomarker validation in patients with colorectal cancer (CRC). MATERIAL AND METHODS: Plasma samples from patients with stage I to IV CRC, with (n = 31) and without (n = 29) disease dissemination at diagnosis or later, were analyzed with SP-PLA using 35 antibodies targeting an equal number of proteins in 5-μl plasma samples. Carcinoembryonic antigen (CEA), analyzed earlier in this cohort using a different technology, was used as a reference. RESULTS: A total of 21 of the 35 investigated proteins were detectable with SP-PLA. Patients in stage II to III with disseminated disease had lower plasma concentrations of HCC-4 (P = .025). Low plasma levels of tissue inhibitor of metalloproteinases–1 were seen in patients with disseminated disease stage II (P = .003). The level of CEA was higher in patients with disease dissemination compared with those without (P = .007). CONCLUSION: SP-PLA has the ability to analyze many protein markers simultaneously in a small amount of blood. However, none of the markers selected for the present SP-PLA analyses gave better prognostic information than CEA. Neoplasia Press 2016-06-04 /pmc/articles/PMC4907971/ /pubmed/27267845 http://dx.doi.org/10.1016/j.tranon.2016.04.001 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original article
Ghanipour, Lana
Darmanis, Spyros
Landegren, Ulf
Glimelius, Bengt
Påhlman, Lars
Birgisson, Helgi
Detection of Biomarkers with Solid-Phase Proximity Ligation Assay in Patients with Colorectal Cancer
title Detection of Biomarkers with Solid-Phase Proximity Ligation Assay in Patients with Colorectal Cancer
title_full Detection of Biomarkers with Solid-Phase Proximity Ligation Assay in Patients with Colorectal Cancer
title_fullStr Detection of Biomarkers with Solid-Phase Proximity Ligation Assay in Patients with Colorectal Cancer
title_full_unstemmed Detection of Biomarkers with Solid-Phase Proximity Ligation Assay in Patients with Colorectal Cancer
title_short Detection of Biomarkers with Solid-Phase Proximity Ligation Assay in Patients with Colorectal Cancer
title_sort detection of biomarkers with solid-phase proximity ligation assay in patients with colorectal cancer
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907971/
https://www.ncbi.nlm.nih.gov/pubmed/27267845
http://dx.doi.org/10.1016/j.tranon.2016.04.001
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