Application of Targeted Next-generation Sequencing, TruSeq Custom Amplicon Assay for Molecular Pathology Diagnostics on Formalin-fixed and Paraffin-embedded Samples

被引:7
作者
Csernak, Erzsebet [1 ]
Molnar, Janos [2 ]
Tusnady, Gabor E. [2 ]
Toth, Erika [1 ]
机构
[1] Natl Inst Oncol, Dept Surg & Mol Pathol, Rath Gy U 7-9, H-1122 Budapest, Hungary
[2] Hungarian Acad Sci, Inst Enzymol, Momentum Membrane Prot Bioinformat Res Grp, Res Ctr Nat Sci, Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
massively parallel sequencing; TruSeq Custom Amplicon assay; molecular pathology; FFPE tissue;
D O I
10.1097/PAI.0000000000000325
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The implementation of targeted therapies revolutionized oncology. As the number of new oncogenic driver mutations, which provide molecular targets for prediction of effective and selective therapies, is increasing, the implementation of fast and reliable methods by molecular pathology labs is very important. Here we report our results with TruSeq Custom Amplicon assay performed on formalin-fixed and paraffin-embedded material. The oligo capture probes targeted the hotspot regions of 10 well-known oncogenes linked to clinical diagnosis and treatment of lung and colorectal adenocarcinomas, melanomas, and gastrointestinal stromal tumors. Fifteen previously genotyped formalin-fixed and paraffin-embedded DNA samples from different tumor types were selected for massively parallel sequencing. A bioinformatics pipeline was developed to identify high-quality variants and remove sequence artifacts. With the exception of 1 sample, which was of lower quality than the others, relevant mutations corresponding to tumor types could be reliable detected by the developed bioinformatical pipeline. This study indicates that the application of TruSeq Custom Amplicon assay is a promising tool in molecular pathology diagnostics, but it is important to standardize sample processing (including fixation, isolation procedure, sample selection based on quality assessment, and rigorous variant calling) to achieve the highest success rate and avoid false results.
引用
收藏
页码:460 / 466
页数:7
相关论文
共 12 条
[1]   Ensembl 2014 [J].
Flicek, Paul ;
Amode, M. Ridwan ;
Barrell, Daniel ;
Beal, Kathryn ;
Billis, Konstantinos ;
Brent, Simon ;
Carvalho-Silva, Denise ;
Clapham, Peter ;
Coates, Guy ;
Fitzgerald, Stephen ;
Gil, Laurent ;
Giron, Carlos Garcia ;
Gordon, Leo ;
Hourlier, Thibaut ;
Hunt, Sarah ;
Johnson, Nathan ;
Juettemann, Thomas ;
Kaehaeri, Andreas K. ;
Keenan, Stephen ;
Kulesha, Eugene ;
Martin, Fergal J. ;
Maurel, Thomas ;
McLaren, William M. ;
Murphy, Daniel N. ;
Nag, Rishi ;
Overduin, Bert ;
Pignatelli, Miguel ;
Pritchard, Bethan ;
Pritchard, Emily ;
Riat, Harpreet S. ;
Ruffier, Magali ;
Sheppard, Daniel ;
Taylor, Kieron ;
Thormann, Anja ;
Trevanion, Stephen J. ;
Vullo, Alessandro ;
Wilder, Steven P. ;
Wilson, Mark ;
Zadissa, Amonida ;
Aken, Bronwen L. ;
Birney, Ewan ;
Cunningham, Fiona ;
Harrow, Jennifer ;
Herrero, Javier ;
Hubbard, Tim J. P. ;
Kinsella, Rhoda ;
Muffato, Matthieu ;
Parker, Anne ;
Spudich, Giulietta ;
Yates, Andy .
NUCLEIC ACIDS RESEARCH, 2014, 42 (D1) :D749-D755
[2]   Next-Generation Sequencing of RNA and DNA Isolated from Paired Fresh-Frozen and Formalin-Fixed Paraffin-Embedded Samples of Human Cancer and Normal Tissue [J].
Hedegaard, Jakob ;
Thorsen, Kasper ;
Lund, Mette Katrine ;
Hein, Anne-Mette K. ;
Hamilton-Dutoit, Stephen Jacques ;
Vang, Soren ;
Nordentoft, Iver ;
Birkenkamp-Demtroder, Karin ;
Kruhoffer, Mogens ;
Hager, Henrik ;
Knudsen, Bjarne ;
Andersen, Claus Lindbjerg ;
Sorensen, Karina Dalsgaard ;
Pedersen, Jakob Skou ;
Orntoft, Torben Falck ;
Dyrskjot, Lars .
PLOS ONE, 2014, 9 (05)
[3]   Linear amplification for deep sequencing [J].
Hoeijmakers, Wieteke A. M. ;
Bartfai, Richard ;
Francoijs, Kees-Jan ;
Stunnenberg, Hendrik G. .
NATURE PROTOCOLS, 2011, 6 (07) :1026-1036
[4]   Targeted high throughput sequencing in clinical cancer Settings: formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity [J].
Kerick, Martin ;
Isau, Melanie ;
Timmermann, Bernd ;
Sueltmann, Holger ;
Herwig, Ralf ;
Krobitsch, Sylvia ;
Schaefer, Georg ;
Verdorfer, Irmgard ;
Bartsch, Georg ;
Klocker, Helmut ;
Lehrach, Hans ;
Schweiger, Michal R. .
BMC MEDICAL GENOMICS, 2011, 4
[5]  
Li H, 2009, BIOINFORMATICS, V25, P1094, DOI [10.1093/bioinformatics/btp100, 10.1093/bioinformatics/btp324]
[6]   Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor [J].
McLaren, William ;
Pritchard, Bethan ;
Rios, Daniel ;
Chen, Yuan ;
Flicek, Paul ;
Cunningham, Fiona .
BIOINFORMATICS, 2010, 26 (16) :2069-2070
[7]  
Meldrum Cliff, 2011, Clin Biochem Rev, V32, P177
[8]   Integrative genomics viewer [J].
Robinson, James T. ;
Thorvaldsdottir, Helga ;
Winckler, Wendy ;
Guttman, Mitchell ;
Lander, Eric S. ;
Getz, Gad ;
Mesirov, Jill P. .
NATURE BIOTECHNOLOGY, 2011, 29 (01) :24-26
[9]   A high frequency of sequence alterations is due to formalin fixation of archival specimens [J].
Williams, C ;
Pontén, F ;
Moberg, C ;
Söderkvist, P ;
Uhlén, M ;
Pontén, J ;
Sitbon, G ;
Lundeberg, J .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (05) :1467-1471
[10]   Targeted-capture massively-parallel sequencing enables robust detection of clinically informative mutations from formalin-fixed tumours [J].
Wong, Stephen Q. ;
Li, Jason ;
Salemi, Renato ;
Sheppard, Karen E. ;
Do, Hongdo ;
Tothill, Richard W. ;
McArthur, Grant A. ;
Dobrovic, Alexander .
SCIENTIFIC REPORTS, 2013, 3