Oligonucleotide array outperforms SNP array on formalin-fixed paraffin-embedded clinical samples

被引:10
|
作者
Nasri, Soroush [1 ]
Anjomshoaa, Ahmad [1 ]
Song, Sarah [1 ]
Guilford, Parry [1 ]
McNoe, Les
Black, Michael
Phillips, Vicky [2 ]
Reeve, Anthony [1 ]
Humar, Bostjan [1 ]
机构
[1] Univ Otago, Canc Genet Lab, Dept Biochem, Dunedin 9054, New Zealand
[2] Otago Sch Med, Dept Surg, Dunedin 9016, New Zealand
关键词
COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER; WIDE; DNA; SINGLE;
D O I
10.1016/j.cancergencyto.2009.12.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Compromised quality of formalin-fixed paraffin-embedded (FFPE)-derived DNA has compounded the use of archival specimens for array-based genomic studies. Recent technological advances have led to first successes in this field; however, there is currently no general agreement on the most suitable platform for the array-based analysis of FFPE DNA. In this study, FFPE and matched fresh-frozen (FF) specimens were separately analyzed with Affymetrix single nucleotide polymorphism (SNP) 6.0 and Agilent 4x44 K oligonucleotide arrays to compare the genomic profiles from the two tissue sources and to assess the relative performance of the two platforms on FFPE material. Genomic DNA was extracted from matched FFPE FF pairs of normal intestinal epithelium from four patients and were applied to the SNP and oligonucleotide platforms according to the manufacturer-recommended protocols. On the Affymetrix platform, a substantial increase in apparent copy number alterations was observed in all FFPE tissues relative to their matched FF counterparts. In contrast, FFPE and matched FF genomic profiles obtained via the Agilent platform were very similar. Both the SNP and the oligonucleotide platform performed comparably on FF material. This study demonstrates that Agilent oligonucleotide array comparative genomic hybridization generates reliable results from FFPE extracted DNA, whereas the Affymetrix SNP-based array seems less suitable for the analysis of FFPE material. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
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