DNA Quality Assessment for Array CGH by Isothermal Whole Genome Amplification

Background: Array Comparative Genomic Hybridization (array CGH) is increasingly applied on DNA obtained from formalin-fixed paraffin-embedded (FFPE) tissue, but in a proportion of cases this type of DNA is unsuitable. Due to the high experimental costs of array CGH and unreliable methods for DNA qua...

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Main Authors: Tineke E. Buffart, Marianne Tijssen, Thijs Krugers, Beatriz Carvalho, Serge J. Smeets, Ruud H. Brakenhoff, Heike Grabsch, Gerrit A. Meijer, Henry B. Sadowski, Bauke Ylstra
Format: Article
Language:English
Published: Wiley 2007-01-01
Series:Cellular Oncology
Online Access:http://dx.doi.org/10.1155/2007/709290
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author Tineke E. Buffart
Marianne Tijssen
Thijs Krugers
Beatriz Carvalho
Serge J. Smeets
Ruud H. Brakenhoff
Heike Grabsch
Gerrit A. Meijer
Henry B. Sadowski
Bauke Ylstra
author_facet Tineke E. Buffart
Marianne Tijssen
Thijs Krugers
Beatriz Carvalho
Serge J. Smeets
Ruud H. Brakenhoff
Heike Grabsch
Gerrit A. Meijer
Henry B. Sadowski
Bauke Ylstra
author_sort Tineke E. Buffart
collection DOAJ
description Background: Array Comparative Genomic Hybridization (array CGH) is increasingly applied on DNA obtained from formalin-fixed paraffin-embedded (FFPE) tissue, but in a proportion of cases this type of DNA is unsuitable. Due to the high experimental costs of array CGH and unreliable methods for DNA quality testing, better prediction methods are needed. The aim of this study was to accurately determine the quality of FFPE DNA input in order to predict quality of array CGH outcome. Material and Methods: DNA quality was assessed by isothermal amplification and compared to array CGH quality on 59 FFPE gastric cancer samples, one FFPE colorectal cancer sample, two FFPE normal uvula samples, one fresh frozen and six FFPE HNSCC samples. Gastric cancer DNA was also quality tested by β-globin PCR. Results: Accurate prediction of DNA quality using the isothermal amplification was observed in the colorectal carcinoma, HNSCC and uvula samples. In gastric cancer samples, the isothermal amplification was a more accurate method for selecting good quality DNA for array CGH compared to using PCR product lengths. The isothermal amplification product was used for array CGH and compared to the results achieved using non-amplified DNA in four of the samples. DNAs before and after amplification yielded the same segmentation patterns of chromosomal copy number changes for both the fresh DNA sample and the FFPE samples. Conclusion: The efficiency of isothermal DNA amplification is a reliable predictor for array CGH quality. The amplification product itself can be used for array CGH, even starting with FFPE derived DNA samples.
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spelling doaj-art-f1390079120542e990a4edd08ba42c4d2025-02-03T01:01:56ZengWileyCellular Oncology1570-58701875-86062007-01-0129435135910.1155/2007/709290DNA Quality Assessment for Array CGH by Isothermal Whole Genome AmplificationTineke E. Buffart0Marianne Tijssen1Thijs Krugers2Beatriz Carvalho3Serge J. Smeets4Ruud H. Brakenhoff5Heike Grabsch6Gerrit A. Meijer7Henry B. Sadowski8Bauke Ylstra9Department of Pathology, VU University Medical Center, Amsterdam, The NetherlandsDepartment of Pathology, VU University Medical Center, Amsterdam, The NetherlandsDepartment of Pathology, VU University Medical Center, Amsterdam, The NetherlandsDepartment of Pathology, VU University Medical Center, Amsterdam, The NetherlandsDepartment of Otolaryngology/Head–Neck Surgery, VU University Medical Center, Amsterdam, The NetherlandsDepartment of Otolaryngology/Head–Neck Surgery, VU University Medical Center, Amsterdam, The NetherlandsPathology and Tumour Biology, Leeds Institute of Molecular Medicine, University of Leeds, UKDepartment of Pathology, VU University Medical Center, Amsterdam, The NetherlandsENZO Life Sciences, Farmingdale, NY, USADepartment of Pathology, VU University Medical Center, Amsterdam, The NetherlandsBackground: Array Comparative Genomic Hybridization (array CGH) is increasingly applied on DNA obtained from formalin-fixed paraffin-embedded (FFPE) tissue, but in a proportion of cases this type of DNA is unsuitable. Due to the high experimental costs of array CGH and unreliable methods for DNA quality testing, better prediction methods are needed. The aim of this study was to accurately determine the quality of FFPE DNA input in order to predict quality of array CGH outcome. Material and Methods: DNA quality was assessed by isothermal amplification and compared to array CGH quality on 59 FFPE gastric cancer samples, one FFPE colorectal cancer sample, two FFPE normal uvula samples, one fresh frozen and six FFPE HNSCC samples. Gastric cancer DNA was also quality tested by β-globin PCR. Results: Accurate prediction of DNA quality using the isothermal amplification was observed in the colorectal carcinoma, HNSCC and uvula samples. In gastric cancer samples, the isothermal amplification was a more accurate method for selecting good quality DNA for array CGH compared to using PCR product lengths. The isothermal amplification product was used for array CGH and compared to the results achieved using non-amplified DNA in four of the samples. DNAs before and after amplification yielded the same segmentation patterns of chromosomal copy number changes for both the fresh DNA sample and the FFPE samples. Conclusion: The efficiency of isothermal DNA amplification is a reliable predictor for array CGH quality. The amplification product itself can be used for array CGH, even starting with FFPE derived DNA samples.http://dx.doi.org/10.1155/2007/709290
spellingShingle Tineke E. Buffart
Marianne Tijssen
Thijs Krugers
Beatriz Carvalho
Serge J. Smeets
Ruud H. Brakenhoff
Heike Grabsch
Gerrit A. Meijer
Henry B. Sadowski
Bauke Ylstra
DNA Quality Assessment for Array CGH by Isothermal Whole Genome Amplification
Cellular Oncology
title DNA Quality Assessment for Array CGH by Isothermal Whole Genome Amplification
title_full DNA Quality Assessment for Array CGH by Isothermal Whole Genome Amplification
title_fullStr DNA Quality Assessment for Array CGH by Isothermal Whole Genome Amplification
title_full_unstemmed DNA Quality Assessment for Array CGH by Isothermal Whole Genome Amplification
title_short DNA Quality Assessment for Array CGH by Isothermal Whole Genome Amplification
title_sort dna quality assessment for array cgh by isothermal whole genome amplification
url http://dx.doi.org/10.1155/2007/709290
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