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Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue
Formalin-fixed, paraffin-embedded (FFPE) tissues are an invaluable resource for clinical research. However, nucleic acids extracted from FFPE tissues are fragmented and chemically modified making them challenging to use in molecular studies. We analysed 23 fresh-frozen (FF), 35 FFPE and 38 paired FF...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039489/ https://www.ncbi.nlm.nih.gov/pubmed/24878701 http://dx.doi.org/10.1371/journal.pone.0098187 |
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author | Hedegaard, Jakob Thorsen, Kasper Lund, Mette Katrine Hein, Anne-Mette K. Hamilton-Dutoit, Stephen Jacques Vang, Søren Nordentoft, Iver Birkenkamp-Demtröder, Karin Kruhøffer, Mogens Hager, Henrik Knudsen, Bjarne Andersen, Claus Lindbjerg Sørensen, Karina Dalsgaard Pedersen, Jakob Skou Ørntoft, Torben Falck Dyrskjøt, Lars |
author_facet | Hedegaard, Jakob Thorsen, Kasper Lund, Mette Katrine Hein, Anne-Mette K. Hamilton-Dutoit, Stephen Jacques Vang, Søren Nordentoft, Iver Birkenkamp-Demtröder, Karin Kruhøffer, Mogens Hager, Henrik Knudsen, Bjarne Andersen, Claus Lindbjerg Sørensen, Karina Dalsgaard Pedersen, Jakob Skou Ørntoft, Torben Falck Dyrskjøt, Lars |
author_sort | Hedegaard, Jakob |
collection | PubMed |
description | Formalin-fixed, paraffin-embedded (FFPE) tissues are an invaluable resource for clinical research. However, nucleic acids extracted from FFPE tissues are fragmented and chemically modified making them challenging to use in molecular studies. We analysed 23 fresh-frozen (FF), 35 FFPE and 38 paired FF/FFPE specimens, representing six different human tissue types (bladder, prostate and colon carcinoma; liver and colon normal tissue; reactive tonsil) in order to examine the potential use of FFPE samples in next-generation sequencing (NGS) based retrospective and prospective clinical studies. Two methods for DNA and three methods for RNA extraction from FFPE tissues were compared and were found to affect nucleic acid quantity and quality. DNA and RNA from selected FFPE and paired FF/FFPE specimens were used for exome and transcriptome analysis. Preparations of DNA Exome-Seq libraries was more challenging (29.5% success) than that of RNA-Seq libraries, presumably because of modifications to FFPE tissue-derived DNA. Libraries could still be prepared from RNA isolated from two-decade old FFPE tissues. Data were analysed using the CLC Bio Genomics Workbench and revealed systematic differences between FF and FFPE tissue-derived nucleic acid libraries. In spite of this, pairwise analysis of DNA Exome-Seq data showed concordance for 70–80% of variants in FF and FFPE samples stored for fewer than three years. RNA-Seq data showed high correlation of expression profiles in FF/FFPE pairs (Pearson Correlations of 0.90 +/- 0.05), irrespective of storage time (up to 244 months) and tissue type. A common set of 1,494 genes was identified with expression profiles that were significantly different between paired FF and FFPE samples irrespective of tissue type. Our results are promising and suggest that NGS can be used to study FFPE specimens in both prospective and retrospective archive-based studies in which FF specimens are not available. |
format | Online Article Text |
id | pubmed-4039489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40394892014-06-02 Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue Hedegaard, Jakob Thorsen, Kasper Lund, Mette Katrine Hein, Anne-Mette K. Hamilton-Dutoit, Stephen Jacques Vang, Søren Nordentoft, Iver Birkenkamp-Demtröder, Karin Kruhøffer, Mogens Hager, Henrik Knudsen, Bjarne Andersen, Claus Lindbjerg Sørensen, Karina Dalsgaard Pedersen, Jakob Skou Ørntoft, Torben Falck Dyrskjøt, Lars PLoS One Research Article Formalin-fixed, paraffin-embedded (FFPE) tissues are an invaluable resource for clinical research. However, nucleic acids extracted from FFPE tissues are fragmented and chemically modified making them challenging to use in molecular studies. We analysed 23 fresh-frozen (FF), 35 FFPE and 38 paired FF/FFPE specimens, representing six different human tissue types (bladder, prostate and colon carcinoma; liver and colon normal tissue; reactive tonsil) in order to examine the potential use of FFPE samples in next-generation sequencing (NGS) based retrospective and prospective clinical studies. Two methods for DNA and three methods for RNA extraction from FFPE tissues were compared and were found to affect nucleic acid quantity and quality. DNA and RNA from selected FFPE and paired FF/FFPE specimens were used for exome and transcriptome analysis. Preparations of DNA Exome-Seq libraries was more challenging (29.5% success) than that of RNA-Seq libraries, presumably because of modifications to FFPE tissue-derived DNA. Libraries could still be prepared from RNA isolated from two-decade old FFPE tissues. Data were analysed using the CLC Bio Genomics Workbench and revealed systematic differences between FF and FFPE tissue-derived nucleic acid libraries. In spite of this, pairwise analysis of DNA Exome-Seq data showed concordance for 70–80% of variants in FF and FFPE samples stored for fewer than three years. RNA-Seq data showed high correlation of expression profiles in FF/FFPE pairs (Pearson Correlations of 0.90 +/- 0.05), irrespective of storage time (up to 244 months) and tissue type. A common set of 1,494 genes was identified with expression profiles that were significantly different between paired FF and FFPE samples irrespective of tissue type. Our results are promising and suggest that NGS can be used to study FFPE specimens in both prospective and retrospective archive-based studies in which FF specimens are not available. Public Library of Science 2014-05-30 /pmc/articles/PMC4039489/ /pubmed/24878701 http://dx.doi.org/10.1371/journal.pone.0098187 Text en © 2014 Hedegaard et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hedegaard, Jakob Thorsen, Kasper Lund, Mette Katrine Hein, Anne-Mette K. Hamilton-Dutoit, Stephen Jacques Vang, Søren Nordentoft, Iver Birkenkamp-Demtröder, Karin Kruhøffer, Mogens Hager, Henrik Knudsen, Bjarne Andersen, Claus Lindbjerg Sørensen, Karina Dalsgaard Pedersen, Jakob Skou Ørntoft, Torben Falck Dyrskjøt, Lars Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue |
title | Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue |
title_full | Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue |
title_fullStr | Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue |
title_full_unstemmed | Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue |
title_short | Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue |
title_sort | next-generation sequencing of rna and dna isolated from paired fresh-frozen and formalin-fixed paraffin-embedded samples of human cancer and normal tissue |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039489/ https://www.ncbi.nlm.nih.gov/pubmed/24878701 http://dx.doi.org/10.1371/journal.pone.0098187 |
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