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CGH arrays compared for DNA isolated from formalin-fixed, paraffin-embedded material.
Krijgsman, Oscar; Israeli, Danielle; Haan, Josien C; van Essen, Hendrik F; Smeets, Serge J; Eijk, Paul P; Steenbergen, Renske D M; Kok, Klaas; Tejpar, Sabine; Meijer, Gerrit A; Ylstra, Bauke.
Afiliação
  • Krijgsman O; Department of Pathology, VU University Medical Center, Amsterdam, The Netherlands.
Genes Chromosomes Cancer ; 51(4): 344-52, 2012 Apr.
Article em En | MEDLINE | ID: mdl-22162309
ABSTRACT
Formalin-fixed, paraffin-embedded (FFPE) archival tissue is an important source of DNA material. The most commonly used technique to identify copy number aberrations from chromosomal DNA in tumorigenesis is array comparative genomic hybridization (aCGH). Although copy number analysis using DNA from FFPE archival tissue is challenging, several research groups have reported high quality and reproducible DNA copy number results using aCGH. Aim of this study is to compare the commercially available aCGH platforms suitable for high-resolution copy number analysis using FFPE-derived DNA. Two dual channel aCGH platforms (Agilent and NimbleGen) and a single channel SNP-based platform (Affymetrix) were evaluated using seven FFPE colon cancer samples, and median absolute deviation (MAD), deflection, signal-to-noise ratio, and DNA input requirements were used as quality criteria. Large differences were observed between platforms; Agilent and NimbleGen showed better MAD values (0.13 for both) compared with Affymetrix (0.22). On the contrary, Affymetrix showed a better deflection of 0.94, followed by 0.71 for Agilent and 0.51 for NimbleGen. This resulted in signal-to-nose ratios that were comparable between the three commercially available platforms. Interestingly, DNA input amounts from FFPE material lower than recommended still yielded high quality profiles on all platforms. Copy number analysis using DNA derived from FFPE archival material is feasible using all three high-resolution copy number platforms and shows reproducible results, also with DNA input amounts lower than recommended.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Preservação de Tecido / DNA / Neoplasias do Colo / Hibridização Genômica Comparativa / Variações do Número de Cópias de DNA Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Genes Chromosomes Cancer Assunto da revista: BIOLOGIA MOLECULAR / NEOPLASIAS Ano de publicação: 2012 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Preservação de Tecido / DNA / Neoplasias do Colo / Hibridização Genômica Comparativa / Variações do Número de Cópias de DNA Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Genes Chromosomes Cancer Assunto da revista: BIOLOGIA MOLECULAR / NEOPLASIAS Ano de publicação: 2012 Tipo de documento: Article País de afiliação: Holanda