Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysis. Export

@article{citeulike:4533466, abstract = {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.}, author = {Schweiger, Michal R. and Kerick, Martin and Timmermann, Bernd and Albrecht, Marcus W. and Borodina, Tatjana and Parkhomchuk, Dmitri and Zatloukal, Kurt and Lehrach, Hans}, citeulike-article-id = {4533466}, citeulike-linkout-0 = {http://dx.doi.org/10.1371/journal.pone.0005548}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/19440246}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=19440246}, doi = {10.1371/journal.pone.0005548}, issn = {1932-6203}, journal = {PloS one}, keywords = {copy-number, deep\_sequencing, ffpe, mutation, technology}, number = {5}, posted-at = {2009-11-08 23:11:35}, priority = {2}, title = {Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysis.}, url = {http://dx.doi.org/10.1371/journal.pone.0005548}, volume = {4}, year = {2009} }

TY - JOUR ID - citeulike:4533466 L3 - citeulike-article-id:4533466 N2 - 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. IS - 5 JF - PloS one SN - 1932-6203 TI - Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysis. VL - 4 KW - copy-number KW - deep_sequencing KW - ffpe KW - mutation KW - technology AU - Schweiger, Michal AU - Kerick, Martin AU - Timmermann, Bernd AU - Albrecht, Marcus AU - Borodina, Tatjana AU - Parkhomchuk, Dmitri AU - Zatloukal, Kurt AU - Lehrach, Hans PY - 2009/// UR - http://dx.doi.org/10.1371/journal.pone.0005548 ER -