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Development of a semi-conductor sequencing-based panel for genotyping of colon and lung cancer by the Onconetwork consortium.
Tops, Bastiaan B J; Normanno, Nicola; Kurth, Henriette; Amato, Eliana; Mafficini, Andrea; Rieber, Nora; Le Corre, Delphine; Rachiglio, Anna Maria; Reiman, Anne; Sheils, Orla; Noppen, Christoph; Lacroix, Ludovic; Cree, Ian A; Scarpa, Aldo; Ligtenberg, Marjolijn J L; Laurent-Puig, Pierre.
Afiliação
  • Tops BB; Department of Pathology, Radboud University Medical Centre (Radboudumc), PO box 9101, 6500 HB, Nijmegen, The Netherlands. bastiaan.tops@radboudumc.nl.
  • Normanno N; Cell Biology and Biotherapy Unit, Istituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione Giovanni Pascale", IRCCS, 80131, Naples, Italy. nicnorm@yahoo.com.
  • Kurth H; Pharmacogenomic Laboratory, CROM - Centro Ricerche Oncologiche di Mercogliano, Mercogliano, 83013, Avellino, Italy. nicnorm@yahoo.com.
  • Amato E; VIOLLIER, Department of Genetics/Molecular Biology, Basle, Switzerland. henriette.kurth@viollier.ch.
  • Mafficini A; ARC-NET Miriam Cherubini Research Centre, University of Verona, Verona, Italy. eliana.amato@univr.it.
  • Rieber N; ARC-NET Miriam Cherubini Research Centre, University of Verona, Verona, Italy. andrea.mafficini@univr.it.
  • Le Corre D; Division of Theoretical Bioinformatics, German Cancer Research Center (DKFZ), 69120, Heidelberg, Germany. n.rieber@dkfz-heidelberg.de.
  • Rachiglio AM; Paris Sorbonne Cité; INSERM UMR-S775, Bases moléculaires des la réponses aux xénobiotiques, Paris, France. delphine.lecorre@parisdescartes.fr.
  • Reiman A; Cell Biology and Biotherapy Unit, Istituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione Giovanni Pascale", IRCCS, 80131, Naples, Italy. anmarachiglio@yahoo.it.
  • Sheils O; Department of Pathology, Warwick Medical School, University Hospitals Coventry and Warwickshire, Coventry, CV2 2DX, UK. a.reiman@warwick.ac.uk.
  • Noppen C; Department of Histopathology, The University of Dublin, Trinity College, Dublin, Ireland. osheils@tcd.ie.
  • Lacroix L; VIOLLIER, Department of Genetics/Molecular Biology, Basle, Switzerland. christoph.noppen@viollier.ch.
  • Cree IA; Department of Medical Biology and Pathology, Translational research Laboratory and Biobank (UMS3655 CNRS/US23 INSERM), INSERM Unit U981, Gustave Roussy, Villejuif, France. ludovic.lacroix@igr.fr.
  • Scarpa A; Department of Pathology, Warwick Medical School, University Hospitals Coventry and Warwickshire, Coventry, CV2 2DX, UK. i.a.cree@warwick.ac.uk.
  • Ligtenberg MJ; ARC-NET Miriam Cherubini Research Centre, University of Verona, Verona, Italy. aldo.scarpa@univr.it.
  • Laurent-Puig P; Department of Pathology and Diagnostics, University of Verona, Verona, Italy. aldo.scarpa@univr.it.
BMC Cancer ; 15: 26, 2015 Jan 31.
Article em En | MEDLINE | ID: mdl-25637035
ABSTRACT

BACKGROUND:

The number of predictive biomarkers that will be necessary to assess in clinical practice will increase with the availability of drugs that target specific molecular alterations. Therefore, diagnostic laboratories are confronted with new challenges costs, turn-around-time and the amount of material required for testing will increase with the number of tests performed on a sample. Our consortium of European clinical research laboratories set out to test if semi-conductor sequencing provides a solution for these challenges.

METHODS:

We designed a multiplex PCR targeting 87 hotspot regions in 22 genes that are of clinical interest for lung and/or colorectal cancer. The gene-panel was tested by 7 different labs in their own clinical setting using ion-semiconductor sequencing.

RESULTS:

We analyzed 155 samples containing 112 previously identified mutations in the KRAS, EGFR en BRAF genes. Only 1 sample failed analysis due to poor quality of the DNA. All other samples were correctly genotyped for the known mutations, even as low as 2%, but also revealed other mutations. Optimization of the primers used in the multiplex PCR resulted in a uniform coverage distribution over the amplicons that allows for efficient pooling of samples in a sequencing run.

CONCLUSIONS:

We show that a semi-conductor based sequencing approach to stratify colon and lung cancer patients is feasible in a clinical setting.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / Sequenciamento de Nucleotídeos em Larga Escala / Técnicas de Genotipagem / Neoplasias Pulmonares Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias do Colo / Sequenciamento de Nucleotídeos em Larga Escala / Técnicas de Genotipagem / Neoplasias Pulmonares Idioma: En Ano de publicação: 2015 Tipo de documento: Article