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Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC
In non-small cell lung cancer (NSCLC) the usage of plasma-derived circulating tumor DNA (ctDNA) have come into focus to obtain a comprehensive genetic profile of a given lung cancer. Despite the usage of specific sampling tubes, archived plasma samples as well as inappropriately treated blood sample...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409026/ https://www.ncbi.nlm.nih.gov/pubmed/32708545 http://dx.doi.org/10.3390/cancers12071917 |
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author | Mayer, Stefanie Schmidtke-Schrezenmeier, Gerlinde Buske, Christian Rücker, Frank G. Barth, Thomas F.E. Möller, Peter Marienfeld, Ralf |
author_facet | Mayer, Stefanie Schmidtke-Schrezenmeier, Gerlinde Buske, Christian Rücker, Frank G. Barth, Thomas F.E. Möller, Peter Marienfeld, Ralf |
author_sort | Mayer, Stefanie |
collection | PubMed |
description | In non-small cell lung cancer (NSCLC) the usage of plasma-derived circulating tumor DNA (ctDNA) have come into focus to obtain a comprehensive genetic profile of a given lung cancer. Despite the usage of specific sampling tubes, archived plasma samples as well as inappropriately treated blood samples still cause a loss of information due to cell lysis and contamination with cellular DNA. Our aim was to establish a reliable protocol to rescue ctDNA from such non-informative samples to monitor the mutational landscape in NSCLC. As a proof-of-concept study we used archived plasma samples derived from whole blood EDTA samples of 51 patients suffering from NSCLC. Analysis of the isolated plasma DNA determined only a small fraction of ctDNA in a range of 90–250 bp. By applying a specific purification procedure, we were able to increase the informative ctDNA content and improve in a cohort of 42 patients the detection of driver mutations from 32% to 79% of the mutations found in tissue biopsies. Thus, we present here an easy to perform, time and cost effective procedure to rescue non-informative ctDNA samples, which is sufficient to detect oncogenic mutations in NGS approaches and is therefore a valuable technical improvement for laboratories handling liquid biopsy samples. |
format | Online Article Text |
id | pubmed-7409026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74090262020-08-26 Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC Mayer, Stefanie Schmidtke-Schrezenmeier, Gerlinde Buske, Christian Rücker, Frank G. Barth, Thomas F.E. Möller, Peter Marienfeld, Ralf Cancers (Basel) Article In non-small cell lung cancer (NSCLC) the usage of plasma-derived circulating tumor DNA (ctDNA) have come into focus to obtain a comprehensive genetic profile of a given lung cancer. Despite the usage of specific sampling tubes, archived plasma samples as well as inappropriately treated blood samples still cause a loss of information due to cell lysis and contamination with cellular DNA. Our aim was to establish a reliable protocol to rescue ctDNA from such non-informative samples to monitor the mutational landscape in NSCLC. As a proof-of-concept study we used archived plasma samples derived from whole blood EDTA samples of 51 patients suffering from NSCLC. Analysis of the isolated plasma DNA determined only a small fraction of ctDNA in a range of 90–250 bp. By applying a specific purification procedure, we were able to increase the informative ctDNA content and improve in a cohort of 42 patients the detection of driver mutations from 32% to 79% of the mutations found in tissue biopsies. Thus, we present here an easy to perform, time and cost effective procedure to rescue non-informative ctDNA samples, which is sufficient to detect oncogenic mutations in NGS approaches and is therefore a valuable technical improvement for laboratories handling liquid biopsy samples. MDPI 2020-07-16 /pmc/articles/PMC7409026/ /pubmed/32708545 http://dx.doi.org/10.3390/cancers12071917 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mayer, Stefanie Schmidtke-Schrezenmeier, Gerlinde Buske, Christian Rücker, Frank G. Barth, Thomas F.E. Möller, Peter Marienfeld, Ralf Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC |
title | Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC |
title_full | Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC |
title_fullStr | Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC |
title_full_unstemmed | Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC |
title_short | Rescue of Non-Informative Circulating Tumor DNA to Monitor the Mutational Landscape in NSCLC |
title_sort | rescue of non-informative circulating tumor dna to monitor the mutational landscape in nsclc |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409026/ https://www.ncbi.nlm.nih.gov/pubmed/32708545 http://dx.doi.org/10.3390/cancers12071917 |
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