Microarray analysis of RNA extracted from formalin-fixed, paraffin-embedded and matched fresh-frozen ovarian adenocarcinomas

<p>Abstract</p> <p>Background</p> <p>Gene expression profiling of formalin-fixed, paraffin-embedded (FFPE) samples represents a valuable approach for advancing oncology diagnostics and enhancing retrospective clinical studies; however, at present, this methodology still...

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Main Authors: Wu Thomas D, Guerrero Steve, Fedorowicz Grazyna, Modrusan Zora
Format: Article
Language:English
Published: BMC 2009-05-01
Series:BMC Medical Genomics
Online Access:http://www.biomedcentral.com/1755-8794/2/23
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spelling doaj-2503711843a14122b2e3ea408c1a80612021-04-02T15:11:55ZengBMCBMC Medical Genomics1755-87942009-05-01212310.1186/1755-8794-2-23Microarray analysis of RNA extracted from formalin-fixed, paraffin-embedded and matched fresh-frozen ovarian adenocarcinomasWu Thomas DGuerrero SteveFedorowicz GrazynaModrusan Zora<p>Abstract</p> <p>Background</p> <p>Gene expression profiling of formalin-fixed, paraffin-embedded (FFPE) samples represents a valuable approach for advancing oncology diagnostics and enhancing retrospective clinical studies; however, at present, this methodology still requires optimization and thus has not been extensively used. Here, we utilized thorough quality control methods to assess RNA extracted from FFPE samples and then compared it to RNA extracted from matched fresh-frozen (FF) counterparts. We preformed genome-wide expression profiling of FF and FFPE ovarian serous adenocarcinoma sample pairs and compared their gene signatures to normal ovary samples.</p> <p>Methods</p> <p>RNA from FFPE samples was extracted using two different methods, Ambion and Agencourt, and its quality was determined by profiling starting total RNA on Bioanalyzer and by amplifying increasing size fragments of <it>beta actin </it>(<it>ACTB</it>) and <it>claudin 3 </it>(<it>CLDN3</it>) by reverse-transcriptase polymerase chain reaction. Five matched FF and FFPE ovarian serous adenocarcinoma samples, as well as a set of normal ovary samples, were profiled using whole genome Agilent microarrays. Reproducibility of the FF and FFPE replicates was measured using Pearson correlation, whereas comparison between the FF and FFPE samples was done using a Z-score analysis.</p> <p>Results</p> <p>Data analysis showed high reproducibility of expression within each FF and FFPE method, whereas matched FF and FFPE pairs demonstrated lower similarity, emphasizing an inherent difference between the two sample types. Z-score analysis of matched FF and FFPE samples revealed good concordance of top 100 differentially expressed genes with the highest correlation of 0.84. Genes characteristic of ovarian serous adenocarcinoma, including a well known marker <it>CLDN3</it>, as well as potentially some novel markers, were identified by comparing gene expression profiles of ovarian adenocarcinoma to those of normal ovary.</p> <p>Conclusion</p> <p>Conclusively, we showed that systematic assessment of FFPE samples at the RNA level is essential for obtaining good quality gene expression microarray data. We also demonstrated that profiling of not only FF but also of FFPE samples can be successfully used to identify differentially expressed genes characteristic of ovarian carcinoma.</p> http://www.biomedcentral.com/1755-8794/2/23
collection DOAJ
language English
format Article
sources DOAJ
author Wu Thomas D
Guerrero Steve
Fedorowicz Grazyna
Modrusan Zora
spellingShingle Wu Thomas D
Guerrero Steve
Fedorowicz Grazyna
Modrusan Zora
Microarray analysis of RNA extracted from formalin-fixed, paraffin-embedded and matched fresh-frozen ovarian adenocarcinomas
BMC Medical Genomics
author_facet Wu Thomas D
Guerrero Steve
Fedorowicz Grazyna
Modrusan Zora
author_sort Wu Thomas D
title Microarray analysis of RNA extracted from formalin-fixed, paraffin-embedded and matched fresh-frozen ovarian adenocarcinomas
title_short Microarray analysis of RNA extracted from formalin-fixed, paraffin-embedded and matched fresh-frozen ovarian adenocarcinomas
title_full Microarray analysis of RNA extracted from formalin-fixed, paraffin-embedded and matched fresh-frozen ovarian adenocarcinomas
title_fullStr Microarray analysis of RNA extracted from formalin-fixed, paraffin-embedded and matched fresh-frozen ovarian adenocarcinomas
title_full_unstemmed Microarray analysis of RNA extracted from formalin-fixed, paraffin-embedded and matched fresh-frozen ovarian adenocarcinomas
title_sort microarray analysis of rna extracted from formalin-fixed, paraffin-embedded and matched fresh-frozen ovarian adenocarcinomas
publisher BMC
series BMC Medical Genomics
issn 1755-8794
publishDate 2009-05-01
description <p>Abstract</p> <p>Background</p> <p>Gene expression profiling of formalin-fixed, paraffin-embedded (FFPE) samples represents a valuable approach for advancing oncology diagnostics and enhancing retrospective clinical studies; however, at present, this methodology still requires optimization and thus has not been extensively used. Here, we utilized thorough quality control methods to assess RNA extracted from FFPE samples and then compared it to RNA extracted from matched fresh-frozen (FF) counterparts. We preformed genome-wide expression profiling of FF and FFPE ovarian serous adenocarcinoma sample pairs and compared their gene signatures to normal ovary samples.</p> <p>Methods</p> <p>RNA from FFPE samples was extracted using two different methods, Ambion and Agencourt, and its quality was determined by profiling starting total RNA on Bioanalyzer and by amplifying increasing size fragments of <it>beta actin </it>(<it>ACTB</it>) and <it>claudin 3 </it>(<it>CLDN3</it>) by reverse-transcriptase polymerase chain reaction. Five matched FF and FFPE ovarian serous adenocarcinoma samples, as well as a set of normal ovary samples, were profiled using whole genome Agilent microarrays. Reproducibility of the FF and FFPE replicates was measured using Pearson correlation, whereas comparison between the FF and FFPE samples was done using a Z-score analysis.</p> <p>Results</p> <p>Data analysis showed high reproducibility of expression within each FF and FFPE method, whereas matched FF and FFPE pairs demonstrated lower similarity, emphasizing an inherent difference between the two sample types. Z-score analysis of matched FF and FFPE samples revealed good concordance of top 100 differentially expressed genes with the highest correlation of 0.84. Genes characteristic of ovarian serous adenocarcinoma, including a well known marker <it>CLDN3</it>, as well as potentially some novel markers, were identified by comparing gene expression profiles of ovarian adenocarcinoma to those of normal ovary.</p> <p>Conclusion</p> <p>Conclusively, we showed that systematic assessment of FFPE samples at the RNA level is essential for obtaining good quality gene expression microarray data. We also demonstrated that profiling of not only FF but also of FFPE samples can be successfully used to identify differentially expressed genes characteristic of ovarian carcinoma.</p>
url http://www.biomedcentral.com/1755-8794/2/23
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