4.1 Article

Short- and long-term reproducibility of the COMET assay for measuring DNA damage biomarkers in frozen blood samples of the EPIC-Heidelberg cohort

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ELSEVIER
DOI: 10.1016/j.mrgentox.2022.503442

Keywords

EPIC; Biobank; Comet assay; Human biomonitoring; DNA damage

Funding

  1. hCOMET (COST Action) [15132]
  2. German Federal Ministry of Education and Research (BMBF) [01ER0809]

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The comet assay is commonly used to evaluate genomic damage, with peripheral blood mononuclear cells (PBMCs) as the preferred cell type. A research center in Germany has a large collection of frozen blood samples from 25 years ago, allowing for retrospective assessment of disease risk factors. Analysis of the Heidelberg-EPIC samples revealed poor correlation in DNA damage between different sampling time points for buffy coat samples, but good correlation for PBMC samples. High BMI was associated with increased DNA damage in PBMCs.
The comet assay is widely used for quantification of genomic damage in humans. Peripheral blood derived mononuclear cells (PBMCs) are the most often used cell type for this purpose. Since the comet assay can be performed in an enhanced throughput format, it can be applied to large sample collections such as biobanks. The European Prospective Investigation into Cancer and Nutrition (EPIC) study is one of the largest existing pro-spective cohort studies, and the German Cancer Research Institute (DKFZ) in Heidelberg is a participating center with 25.000 frozen blood samples stored from around 25 years ago, enabling retrospective assessment of disease risk factors. However, experience with decades long frozen samples in the comet assay is so far missing. In Heidelberg, 800 study participants were re-invited twice between 2010 and 2012 to donate further blood samples. Here, we analyzed 299 Heidelberg-EPIC samples, compiled from frozen PBMC and buffy coat prepa-rations selected from the different sampling time points. In addition, 47 frozen PBMC samples from morbidly obese individuals were included. For buffy coat samples, we observed a poor correlation between DNA damage in the same donors assessed at two sampling time points. Additionally, no correlation between DNA damage in buffy coat samples and PBMCs was found. For PBMCs, a good correlation was observed between samples of the same donors at the two time points. DNA damage was not affected by age and smoking status, but high BMI (>30; obesity) was associated with increased DNA damage in PBMCs. There was no indication for a threshold of a certain BMI for increased DNA damage. In conclusion, while 25 year-long stored buffy coat preparations may require adaptation of certain experimental parameters such as cell density and electrophoresis conditions, frozen PBMC biobank samples can be analyzed in the comet assay even after a decade of storage.

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