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Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development

2003; Springer Nature; Volume: 89; Issue: 10 Linguagem: Inglês

10.1038/sj.bjc.6601374

1532-1827

Wieke Zuidervaart, Pieter A. van der Velden, Monique H.M.H. Hurks, Frans A. van Nieuwpoort, Coby Out‐Luiting, Amartya Singh, Rune R. Frants, Martine J. Jager, Nelleke A. Gruis,

melanin and skin pigmentation

Microarray is a powerful tool to compare the gene expression of different tumour specimens and cell lines simultaneously and quantitatively. To get a better insight into genes that are involved in uveal melanoma tumorigenesis, we compared the gene expression profiles of 12 different uveal melanoma cell lines with three melanocyte cell cultures obtained from healthy donor eyes. Gene expression profiles were obtained by nylon filter arrays, containing 1176 gene spots related to cancer development. The expression levels of selected genes were validated on cell lines and primary uveal melanomas by real time RT–PCR, and were subsequently included in cluster analysis. Four candidate tumour markers, Laminin Receptor 1, Endothelin 2, Von Hippel Lindau Binding protein 1 and Cullin 2, have been selected from genes that were differentially expressed in the uveal melanoma cell lines compared to the normal uveal melanocytes. In primary uveal melanomas, these four markers could discriminate between two classes of uveal melanoma, which may be indicative of a differential disease process.