Cargando…

Genome-Wide Massively Parallel Sequencing of Formaldehyde Fixed-Paraffin Embedded (FFPE) Tumor Tissues for Copy-Number- and Mutation-Analysis

BACKGROUND: Cancer re-sequencing programs rely on DNA isolated from fresh snap frozen tissues, the preparation of which is combined with additional preservation efforts. Tissue samples at pathology departments are routinely stored as formalin-fixed and paraffin-embedded (FFPE) samples and their use...

Descripción completa

Detalles Bibliográficos
Autores principales: Schweiger, Michal R., Kerick, Martin, Timmermann, Bernd, Albrecht, Marcus W., Borodina, Tatjana, Parkhomchuk, Dmitri, Zatloukal, Kurt, Lehrach, Hans
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2678265/
https://www.ncbi.nlm.nih.gov/pubmed/19440246
http://dx.doi.org/10.1371/journal.pone.0005548
_version_ 1782166839230464000
author Schweiger, Michal R.
Kerick, Martin
Timmermann, Bernd
Albrecht, Marcus W.
Borodina, Tatjana
Parkhomchuk, Dmitri
Zatloukal, Kurt
Lehrach, Hans
author_facet Schweiger, Michal R.
Kerick, Martin
Timmermann, Bernd
Albrecht, Marcus W.
Borodina, Tatjana
Parkhomchuk, Dmitri
Zatloukal, Kurt
Lehrach, Hans
author_sort Schweiger, Michal R.
collection PubMed
description BACKGROUND: Cancer re-sequencing programs rely on DNA isolated from fresh snap frozen tissues, the preparation of which is combined with additional preservation efforts. Tissue samples at pathology departments are routinely stored as formalin-fixed and paraffin-embedded (FFPE) samples and their use would open up access to a variety of clinical trials. However, FFPE preparation is incompatible with many down-stream molecular biology techniques such as PCR based amplification methods and gene expression studies. METHODOLOGY/PRINCIPAL FINDINGS: Here we investigated the sample quality requirements of FFPE tissues for massively parallel short-read sequencing approaches. We evaluated key variables of pre-fixation, fixation related and post-fixation processes that occur in routine medical service (e.g. degree of autolysis, duration of fixation and of storage). We also investigated the influence of tissue storage time on sequencing quality by using material that was up to 18 years old. Finally, we analyzed normal and tumor breast tissues using the Sequencing by Synthesis technique (Illumina Genome Analyzer, Solexa) to simultaneously localize genome-wide copy number alterations and to detect genomic variations such as substitutions and point-deletions and/or insertions in FFPE tissue samples. CONCLUSIONS/SIGNIFICANCE: The application of second generation sequencing techniques on small amounts of FFPE material opens up the possibility to analyze tissue samples which have been collected during routine clinical work as well as in the context of clinical trials. This is in particular important since FFPE samples are amply available from surgical tumor resections and histopathological diagnosis, and comprise tissue from precursor lesions, primary tumors, lymphogenic and/or hematogenic metastases. Large-scale studies using this tissue material will result in a better prediction of the prognosis of cancer patients and the early identification of patients which will respond to therapy.
format Text
id pubmed-2678265
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-26782652009-05-14 Genome-Wide Massively Parallel Sequencing of Formaldehyde Fixed-Paraffin Embedded (FFPE) Tumor Tissues for Copy-Number- and Mutation-Analysis Schweiger, Michal R. Kerick, Martin Timmermann, Bernd Albrecht, Marcus W. Borodina, Tatjana Parkhomchuk, Dmitri Zatloukal, Kurt Lehrach, Hans PLoS One Research Article BACKGROUND: Cancer re-sequencing programs rely on DNA isolated from fresh snap frozen tissues, the preparation of which is combined with additional preservation efforts. Tissue samples at pathology departments are routinely stored as formalin-fixed and paraffin-embedded (FFPE) samples and their use would open up access to a variety of clinical trials. However, FFPE preparation is incompatible with many down-stream molecular biology techniques such as PCR based amplification methods and gene expression studies. METHODOLOGY/PRINCIPAL FINDINGS: Here we investigated the sample quality requirements of FFPE tissues for massively parallel short-read sequencing approaches. We evaluated key variables of pre-fixation, fixation related and post-fixation processes that occur in routine medical service (e.g. degree of autolysis, duration of fixation and of storage). We also investigated the influence of tissue storage time on sequencing quality by using material that was up to 18 years old. Finally, we analyzed normal and tumor breast tissues using the Sequencing by Synthesis technique (Illumina Genome Analyzer, Solexa) to simultaneously localize genome-wide copy number alterations and to detect genomic variations such as substitutions and point-deletions and/or insertions in FFPE tissue samples. CONCLUSIONS/SIGNIFICANCE: The application of second generation sequencing techniques on small amounts of FFPE material opens up the possibility to analyze tissue samples which have been collected during routine clinical work as well as in the context of clinical trials. This is in particular important since FFPE samples are amply available from surgical tumor resections and histopathological diagnosis, and comprise tissue from precursor lesions, primary tumors, lymphogenic and/or hematogenic metastases. Large-scale studies using this tissue material will result in a better prediction of the prognosis of cancer patients and the early identification of patients which will respond to therapy. Public Library of Science 2009-05-14 /pmc/articles/PMC2678265/ /pubmed/19440246 http://dx.doi.org/10.1371/journal.pone.0005548 Text en Schweiger 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
Schweiger, Michal R.
Kerick, Martin
Timmermann, Bernd
Albrecht, Marcus W.
Borodina, Tatjana
Parkhomchuk, Dmitri
Zatloukal, Kurt
Lehrach, Hans
Genome-Wide Massively Parallel Sequencing of Formaldehyde Fixed-Paraffin Embedded (FFPE) Tumor Tissues for Copy-Number- and Mutation-Analysis
title Genome-Wide Massively Parallel Sequencing of Formaldehyde Fixed-Paraffin Embedded (FFPE) Tumor Tissues for Copy-Number- and Mutation-Analysis
title_full Genome-Wide Massively Parallel Sequencing of Formaldehyde Fixed-Paraffin Embedded (FFPE) Tumor Tissues for Copy-Number- and Mutation-Analysis
title_fullStr Genome-Wide Massively Parallel Sequencing of Formaldehyde Fixed-Paraffin Embedded (FFPE) Tumor Tissues for Copy-Number- and Mutation-Analysis
title_full_unstemmed Genome-Wide Massively Parallel Sequencing of Formaldehyde Fixed-Paraffin Embedded (FFPE) Tumor Tissues for Copy-Number- and Mutation-Analysis
title_short Genome-Wide Massively Parallel Sequencing of Formaldehyde Fixed-Paraffin Embedded (FFPE) Tumor Tissues for Copy-Number- and Mutation-Analysis
title_sort genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (ffpe) tumor tissues for copy-number- and mutation-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2678265/
https://www.ncbi.nlm.nih.gov/pubmed/19440246
http://dx.doi.org/10.1371/journal.pone.0005548
work_keys_str_mv AT schweigermichalr genomewidemassivelyparallelsequencingofformaldehydefixedparaffinembeddedffpetumortissuesforcopynumberandmutationanalysis
AT kerickmartin genomewidemassivelyparallelsequencingofformaldehydefixedparaffinembeddedffpetumortissuesforcopynumberandmutationanalysis
AT timmermannbernd genomewidemassivelyparallelsequencingofformaldehydefixedparaffinembeddedffpetumortissuesforcopynumberandmutationanalysis
AT albrechtmarcusw genomewidemassivelyparallelsequencingofformaldehydefixedparaffinembeddedffpetumortissuesforcopynumberandmutationanalysis
AT borodinatatjana genomewidemassivelyparallelsequencingofformaldehydefixedparaffinembeddedffpetumortissuesforcopynumberandmutationanalysis
AT parkhomchukdmitri genomewidemassivelyparallelsequencingofformaldehydefixedparaffinembeddedffpetumortissuesforcopynumberandmutationanalysis
AT zatloukalkurt genomewidemassivelyparallelsequencingofformaldehydefixedparaffinembeddedffpetumortissuesforcopynumberandmutationanalysis
AT lehrachhans genomewidemassivelyparallelsequencingofformaldehydefixedparaffinembeddedffpetumortissuesforcopynumberandmutationanalysis