Expression profiling of formalin-fixed paraffin embedded primary human uveal melanomas using DASL matrices

Expression profiling of formalin-fixed paraffin embedded primary human uveal melanomas using DASL matrices

Autor Di Cesare, Sebastian Google Scholar
Nantel, Andre Google Scholar
Marshall, Jean-Claude Google Scholar
Fernandes, Bruno F. Autor UNIFESP Google Scholar
Antecka, Emilia Google Scholar
Orellana, Maria E. Google Scholar
Abourbih, Daniel Google Scholar
Saornil, Antonia M. Google Scholar
Burnier, Miguel N. Autor UNIFESP Google Scholar
Instituição McGill Univ
Natl Res Council Canada
NCI
Universidade Federal de São Paulo (UNIFESP)
Univ Valladolid
Resumo Fresh biopsied ocular tumor tissues are difficult to obtain for the purpose of performing microarray experiments on extracted nucleic acids. Present technology allows for extraction of total RNA from formalin-fixed paraffin embedded (FFPE) tissue analyzed by the cDNA mediated Annealing Sectioning and Ligation (DASL) method. We aimed to correlate gene transcript differences between two uveal melanoma (UM) clinical-histopathological parameters (metastasis, cell type).A total of 43 FFPE UM were used. the expression of RPL13a, a ribosomal protein gene, for each sample was used to evaluate the quality of RNA extracted from FFPE tissue. Gene expression values generated from the array were analyzed using the GeneSpring GX software (Agilent). Immunohistochemistry was used in order to validate transcriptional findings at the protein level.A total of 106 genes were identified with (P < 0.05, Welch ANOVA test) a difference in transcript abundance for the metastasis clinical parameter. Furthermore, we identified 64 genes with a statistically significant (P < 0.05) difference in transcript abundance between the spindle and epithelioid cell types. Each individual sample for both groups (metastasis, cell type) exhibited distinct transcriptional profiles that were separated on a PCA. Positive nuclear immunostaining for LIG4-metastasis, ErbB3-cell type was found to be associated with better patient prognosis and outcome.To the best of our knowledge, this is the first time that a successful retrospective analysis has been done with UM FFPE RNA. This data may lead to future customized therapeutic targets, which may improve the now unchanged mortality rate of this particular malignancy.
Palavra-chave Uveal melanoma
FFPE
DASL
Expression profiling
Histopathology
Clinical parameters
Idioma Inglês
Financiador Cedars Cancer Institute
Hellen Keller Foundation
Data de publicação 2010-04-01
Publicado em Journal of Cancer Research and Clinical Oncology. New York: Springer, v. 136, n. 4, p. 577-586, 2010.
ISSN 0171-5216 (Sherpa/Romeo, fator de impacto)
Publicador Springer
Extensão 577-586
Fonte http://dx.doi.org/10.1007/s00432-009-0692-3
Direito de acesso Acesso restrito
Tipo Artigo
Web of Science WOS:000274686800012
Endereço permanente http://repositorio.unifesp.br/handle/11600/32408

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