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Evaluation of commercial kits for isolation and bisulfite conversion of circulating cell-free tumor DNA from blood
BACKGROUND: DNA methylation biomarkers in circulating cell-free DNA (cfDNA) have great clinical potential for cancer management. Most methods for DNA methylation analysis require bisulfite conversion, causing DNA degradation and loss. This is particularly challenging for cfDNA, which is naturally fr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503171/ https://www.ncbi.nlm.nih.gov/pubmed/37710283 http://dx.doi.org/10.1186/s13148-023-01563-0 |
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author | Kresse, Stine H. Brandt-Winge, Sara Pharo, Heidi Flatin, Bjørnar T. B. Jeanmougin, Marine Vedeld, Hege Marie Lind, Guro E. |
author_facet | Kresse, Stine H. Brandt-Winge, Sara Pharo, Heidi Flatin, Bjørnar T. B. Jeanmougin, Marine Vedeld, Hege Marie Lind, Guro E. |
author_sort | Kresse, Stine H. |
collection | PubMed |
description | BACKGROUND: DNA methylation biomarkers in circulating cell-free DNA (cfDNA) have great clinical potential for cancer management. Most methods for DNA methylation analysis require bisulfite conversion, causing DNA degradation and loss. This is particularly challenging for cfDNA, which is naturally fragmented and normally present in low amounts. The aim of the present study was to identify an optimal combination of cfDNA isolation and bisulfite conversion kits for downstream analysis of DNA methylation biomarkers in plasma. RESULTS: Of the five tested bisulfite conversion kits (EpiJET Bisulfite Conversion Kit, EpiTect Plus DNA Bisulfite Kit (EpiTect), EZ DNA Methylation-Direct Kit, Imprint DNA Modification Kit (Imprint) and Premium Bisulfite Kit), the highest and lowest DNA yield and recovery were achieved using the EpiTect kit and the Imprint kit, respectively, with more than double the amount of DNA for the EpiTect kit. Of the three tested cfDNA isolation kits (Maxwell RSC ccfDNA Plasma Kit, QIAamp Circulating Nucleic Acid Kit (CNA) and QIAamp MinElute ccfDNA Mini Kit), the CNA kit yielded around twice as much cfDNA compared to the two others kits, although with more high molecular weight DNA present. When comparing various combinations of cfDNA isolation kits and bisulfite conversion kits, the CNA kit and the EpiTect kit were identified as the best-performing combination, resulting in the highest yield of bisulfite converted cfDNA from normal plasma, as measured by droplet digital PCR (ddPCR). As a proof of principle, this kit combination was used to process plasma samples from 13 colorectal cancer patients for subsequent ddPCR methylation analysis of BCAT1 and IKZF1. Methylation of BCAT1 and/or IKZF1 was identified in 6/10 (60%) stage IV patients and 1/3 (33%) stage III patients. CONCLUSIONS: Based on a thorough evaluation of five bisulfite conversion kits and three cfDNA isolation kits, both individually and in combination, the CNA kit and the EpiTect kit were identified as the best-performing kit combination, with highest DNA yield and recovery across a range of DNA input amounts. The combination was successfully used for detection of clinically relevant DNA methylation biomarkers in plasma from cancer patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-023-01563-0. |
format | Online Article Text |
id | pubmed-10503171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105031712023-09-16 Evaluation of commercial kits for isolation and bisulfite conversion of circulating cell-free tumor DNA from blood Kresse, Stine H. Brandt-Winge, Sara Pharo, Heidi Flatin, Bjørnar T. B. Jeanmougin, Marine Vedeld, Hege Marie Lind, Guro E. Clin Epigenetics Research BACKGROUND: DNA methylation biomarkers in circulating cell-free DNA (cfDNA) have great clinical potential for cancer management. Most methods for DNA methylation analysis require bisulfite conversion, causing DNA degradation and loss. This is particularly challenging for cfDNA, which is naturally fragmented and normally present in low amounts. The aim of the present study was to identify an optimal combination of cfDNA isolation and bisulfite conversion kits for downstream analysis of DNA methylation biomarkers in plasma. RESULTS: Of the five tested bisulfite conversion kits (EpiJET Bisulfite Conversion Kit, EpiTect Plus DNA Bisulfite Kit (EpiTect), EZ DNA Methylation-Direct Kit, Imprint DNA Modification Kit (Imprint) and Premium Bisulfite Kit), the highest and lowest DNA yield and recovery were achieved using the EpiTect kit and the Imprint kit, respectively, with more than double the amount of DNA for the EpiTect kit. Of the three tested cfDNA isolation kits (Maxwell RSC ccfDNA Plasma Kit, QIAamp Circulating Nucleic Acid Kit (CNA) and QIAamp MinElute ccfDNA Mini Kit), the CNA kit yielded around twice as much cfDNA compared to the two others kits, although with more high molecular weight DNA present. When comparing various combinations of cfDNA isolation kits and bisulfite conversion kits, the CNA kit and the EpiTect kit were identified as the best-performing combination, resulting in the highest yield of bisulfite converted cfDNA from normal plasma, as measured by droplet digital PCR (ddPCR). As a proof of principle, this kit combination was used to process plasma samples from 13 colorectal cancer patients for subsequent ddPCR methylation analysis of BCAT1 and IKZF1. Methylation of BCAT1 and/or IKZF1 was identified in 6/10 (60%) stage IV patients and 1/3 (33%) stage III patients. CONCLUSIONS: Based on a thorough evaluation of five bisulfite conversion kits and three cfDNA isolation kits, both individually and in combination, the CNA kit and the EpiTect kit were identified as the best-performing kit combination, with highest DNA yield and recovery across a range of DNA input amounts. The combination was successfully used for detection of clinically relevant DNA methylation biomarkers in plasma from cancer patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-023-01563-0. BioMed Central 2023-09-14 /pmc/articles/PMC10503171/ /pubmed/37710283 http://dx.doi.org/10.1186/s13148-023-01563-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kresse, Stine H. Brandt-Winge, Sara Pharo, Heidi Flatin, Bjørnar T. B. Jeanmougin, Marine Vedeld, Hege Marie Lind, Guro E. Evaluation of commercial kits for isolation and bisulfite conversion of circulating cell-free tumor DNA from blood |
title | Evaluation of commercial kits for isolation and bisulfite conversion of circulating cell-free tumor DNA from blood |
title_full | Evaluation of commercial kits for isolation and bisulfite conversion of circulating cell-free tumor DNA from blood |
title_fullStr | Evaluation of commercial kits for isolation and bisulfite conversion of circulating cell-free tumor DNA from blood |
title_full_unstemmed | Evaluation of commercial kits for isolation and bisulfite conversion of circulating cell-free tumor DNA from blood |
title_short | Evaluation of commercial kits for isolation and bisulfite conversion of circulating cell-free tumor DNA from blood |
title_sort | evaluation of commercial kits for isolation and bisulfite conversion of circulating cell-free tumor dna from blood |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10503171/ https://www.ncbi.nlm.nih.gov/pubmed/37710283 http://dx.doi.org/10.1186/s13148-023-01563-0 |
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