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

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• 作者：Lana Ghanipour^* ; ^{arezo_g@hotmail.com" class="auth_mail" title="E-mail the corresponding author} ; Spyros Darmanis^&dagger ; ; Ulf Landegren^&dagger ; ; Bengt Glimelius^&Dagger ; ; Lars På ; hlman^* ; Helgi Birgisson^*
• 刊名：Translational Oncology
• 出版年：2016
• 出版时间：June 2016
• 年：2016
• 卷：9
• 期：3
• 页码：251-255
• 全文大小：277 K

文摘

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.