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Validation of a prognostic multi-gene signature in high-risk neuroblastoma using the high throughput digital NanoString nCounter™ system.
Stricker, Thomas P; Morales La Madrid, Andres; Chlenski, Alexandre; Guerrero, Lisa; Salwen, Helen R; Gosiengfiao, Yasmin; Perlman, Elizabeth J; Furman, Wayne; Bahrami, Armita; Shohet, Jason M; Zage, Peter E; Hicks, M John; Shimada, Hiroyuki; Suganuma, Rie; Park, Julie R; So, Sara; London, Wendy B; Pytel, Peter; Maclean, Kirsteen H; Cohn, Susan L.
Afiliação
  • Stricker TP; Department of Pathology, Microbiology and Immunology, Vanderbilt University, Nashville, TN, USA.
  • Morales La Madrid A; Department of Pediatrics, Comer Children's Hospital, University of Chicago, Chicago, IL, USA.
  • Chlenski A; Department of Pediatrics, Comer Children's Hospital, University of Chicago, Chicago, IL, USA.
  • Guerrero L; Department of Pediatrics, Comer Children's Hospital, University of Chicago, Chicago, IL, USA.
  • Salwen HR; Department of Pediatrics, Comer Children's Hospital, University of Chicago, Chicago, IL, USA.
  • Gosiengfiao Y; Department of Pediatrics, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Perlman EJ; Department of Pathology, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Furman W; Department of Hematology/Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Bahrami A; Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Shohet JM; Department of Pediatrics, Texas Children's Cancer Center, Baylor College of Medicine, Houston, TX, USA.
  • Zage PE; Department of Pediatrics, Texas Children's Cancer Center, Baylor College of Medicine, Houston, TX, USA.
  • Hicks MJ; Department of Pathology, Texas Children's Cancer Center, Baylor College of Medicine, Houston, TX, USA.
  • Shimada H; Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, CA, USA.
  • Suganuma R; Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, CA, USA.
  • Park JR; Department of Pediatrics, Seattle Children's Hospital, University of Washington, Seattle, WA, USA; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • So S; Department of Pediatrics, Seattle Children's Hospital, University of Washington, Seattle, WA, USA; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • London WB; Children's Oncology Group Statistics and Data Center, Boston, MA, USA; Boston Children's Hospital/Dana-Farber Cancer Institute, Boston, MA, USA.
  • Pytel P; Department of Pathology, Comer Children's Hospital, University of Chicago, Chicago, IL, USA.
  • Maclean KH; NanoString Technologies, Seattle, WA, USA.
  • Cohn SL; Department of Pediatrics, Comer Children's Hospital, University of Chicago, Chicago, IL, USA. Electronic address: scohn@peds.bsd.uchicago.edu.
Mol Oncol ; 8(3): 669-78, 2014 May.
Article em En | MEDLINE | ID: mdl-24560446
Microarray-based molecular signatures have not been widely integrated into neuroblastoma diagnostic classification systems due to the complexities of the assay and requirement for high-quality RNA. New digital technologies that accurately quantify gene expression using RNA isolated from formalin-fixed paraffin embedded (FFPE) tissues are now available. In this study, we describe the first use of a high-throughput digital system to assay the expression of genes in an "ultra-high risk" microarray classifier in FFPE high-risk neuroblastoma tumors. Customized probes corresponding to the 42 genes in a published multi-gene neuroblastoma signature were hybridized to RNA isolated from 107 FFPE high-risk neuroblastoma samples using the NanoString nCounter™ Analysis System. For classification of each patient, the Pearson's correlation coefficient was calculated between the standardized nCounter™ data and the molecular signature from the microarray data. We demonstrate that the nCounter™ 42-gene panel sub-stratified the high-risk cohort into two subsets with statistically significantly different overall survival (p = 0.0027) and event-free survival (p = 0.028). In contrast, none of the established prognostic risk markers (age, stage, tumor histology, MYCN status, and ploidy) were significantly associated with survival. We conclude that the nCounter™ System can reproducibly quantify expression levels of signature genes in FFPE tumor samples. Validation of this microarray signature in our high-risk patient cohort using a completely different technology emphasizes the prognostic relevance of this classifier. Prospective studies testing the prognostic value of molecular signatures in high-risk neuroblastoma patients using FFPE tumor samples and the nCounter™ System are warranted.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência com Séries de Oligonucleotídeos / Neuroblastoma Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Infant Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência com Séries de Oligonucleotídeos / Neuroblastoma Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans / Infant Idioma: En Ano de publicação: 2014 Tipo de documento: Article