Abstract

In recent years the blood proteome has been increasingly researched for biomarkers for early detection of colorectal cancer (CRC). Blood samples from screening studies are often subject to preanalytical variability and repeated freeze–thaw cycles. We aimed to assess the correlation of repeat measurements of 27 candidate protein markers for CRC screening taken three years and multiple freeze–thaw cycles apart. The concentrations of 27 protein markers were measured in plasma samples of 39 newly detected CRC cases from a cohort of 9245 participants of screening colonoscopies. The proteins were measured using proximity extension assays (PEA) carried out on the same set of samples twice, three years apart, with an average of three freeze–thaw cycles in between the two measurements. Pearson’s product moment correlation coefficients were calculated. Correlation coefficients ranged from +0.43 to +0.97, with a median of 0.67 and an interquartile range of +0.58 to +0.84, with all p-values of correlation being <0.01 (<0.0005 for 22 proteins, <0.001 for 4 proteins). Repeat measurements of the 27 protein biomarkers for CRC screening performed three years later, and on average three freeze–thaw cycles apart, showed moderate to high levels of correlation. Apart from the effects of freeze–thaw cycles, slightly different preprocessing performed on the data may have contributed to recorded differences between measurements.

Highlights

  • Published: 2 March 2022In recent years the blood proteome has been increasingly researched for biomarkers for early detection of various cancers, including colorectal cancer (CRC) [1–5]

  • In order to determine the effect of freeze–thaw cycles and prolonged sample storage times on expressions of candidate plasma proteins for CRC early detection, concentrations of 27 proteins were directly compared for paired samples from proximity extension assays (PEA) measurements performed in the year 2015 and, after an additional three freeze

  • Paired measurements were available for 39 CRC cases detected at screening colonoscopy

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Summary

Introduction

In recent years the blood proteome has been increasingly researched for biomarkers for early detection of various cancers, including colorectal cancer (CRC) [1–5]. It is often the case in cancer screening studies for blood samples to be stored in freezers and used for multiple measurements of candidate biomarkers for early detection. If the samples are stored in bigger aliquots as a result of space constraints in large-scale screening studies, they may undergo several freeze–thaw cycles before being used for measurements of candidate biomarkers for early detection of cancer. The objective of this study was to assess the effects of preanalytical freeze–thaw cycles on plasma proteins measured as potential biomarkers for CRC early detection among Adverse effects of freeze–thaw cycles are plausible, no previous study has, to the best of our knowledge, empirically assessed their possible impact in cancer screening studies.

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