May 2008
Volume 49, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2008
Epigenetic Regulation Identifies RASEF as Tumor Suppressor Gene in Uveal Melanoma
Author Affiliations & Notes
  • P. A. van der Velden
    LUMC, Leiden, The Netherlands
    Ophthalmology,
  • W. Maat
    LUMC, Leiden, The Netherlands
    Ophthalmology,
  • S. H. W. Beiboer
    Hogeschool Leiden, Leiden, The Netherlands
  • G. P. M. Luyten
    LUMC, Leiden, The Netherlands
    Ophthalmology,
  • N. A. Gruis
    LUMC, Leiden, The Netherlands
    Dermatology,
  • M. J. Jager
    LUMC, Leiden, The Netherlands
    Ophthalmology,
  • Footnotes
    Commercial Relationships  P.A. van der Velden, None; W. Maat, None; S.H.W. Beiboer, None; G.P.M. Luyten, None; N.A. Gruis, None; M.J. Jager, None.
  • Footnotes
    Support  KWF Grant RUL 2001-2472
Investigative Ophthalmology & Visual Science May 2008, Vol.49, 1502. doi:
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      P. A. van der Velden, W. Maat, S. H. W. Beiboer, G. P. M. Luyten, N. A. Gruis, M. J. Jager; Epigenetic Regulation Identifies RASEF as Tumor Suppressor Gene in Uveal Melanoma. Invest. Ophthalmol. Vis. Sci. 2008;49(13):1502.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Recently, a segregation study in families with uveal and cutaneous melanoma identified 9q21 as potential locus to harbor a tumor suppressor gene (TSG). One of the genes in this area, RASEF, was then analyzed as a candidate tumor suppressor gene but lack of point mutations and copy number changes could not confirm this. We investigated the RASEF gene for potential mutations and gene silencing by promotor methylation in uveal melanoma.

Methods: : Eleven uveal melanoma cell lines and 35 primary uveal melanoma samples were screened for mutations in the RASEF gene by high resolution melting curve and digestion analysis. Expression of RASEF was determined by real time RT-PCR in all cell lines and 16 primary uveal melanoma samples, while the methylation status of the promoter of the RASEF gene was analyzed and confirmed by direct sequencing.

Results: : Mutation screening revealed a known polymorphism (R262C; C→T) in exon 5 of the RASEF gene that displayed a normal frequency (54%). Of the primary uveal melanomas, 46% presented a heterozygous genotype, while ten out of eleven cell lines (91%) showed a homozygous genotype. Melting-curve analysis indicated loss of heterozygosity in at least two primary tumors. A low RASEF expression in the cell lines and primary tumors was correlated with methylation of the RASEF promoter region. Homozygosity as well as methylation of the RASEF gene in primary tumors were associated with a decreased survival (P= .019).

Conclusions: : Homozygosity in combination with methylation appears to be the mechanism targeting RASEF in uveal melanoma and allelic imbalance at this locus supports a TSG role for RASEF.

Keywords: candidate gene analysis • melanoma • mutations 
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