Familial Cancer

, Volume 9, Issue 4, pp 663–667

Contribution of CDKN2A/P16INK4A, P14ARF, CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma

  • B. Buecher
  • M. Gauthier-Villars
  • L. Desjardins
  • L. Lumbroso-Le Rouic
  • C. Levy
  • A. De Pauw
  • J. Bombled
  • C. Tirapo
  • C. Houdayer
  • B. Bressac-de Paillerets
  • D. Stoppa-Lyonnet
Article

DOI: 10.1007/s10689-010-9379-9

Cite this article as:
Buecher, B., Gauthier-Villars, M., Desjardins, L. et al. Familial Cancer (2010) 9: 663. doi:10.1007/s10689-010-9379-9

Abstract

Uveal melanoma arises from melanocytes of the uveal tract (iris, ciliary body and choroid) and represents the most common intraocular malignancy in adults. Some rare clinical situations (young age at diagnosis, bilateral or multifocal forms, association with cutaneous malignant melanoma and/or familial aggregations of melanomas) are suggestive of genetic susceptibility. The aim of this study was to evaluate the contribution of CDKN2A/P16INK4A, P14ARF and CDK4 gene germline mutations in a series of patients with uveal melanoma recruited in a single institution with a clinical presentation indicative of genetic predisposition. Molecular analyses were proposed to 36 patients and were performed in 25 cases. The contribution of BRCA1/2 gene germline mutations in patients with uveal melanoma and a personal and/or family history of breast/ovarian cancers was also evaluated. Molecular analysis of BRCA1/2 genes was proposed to 35 patients and was performed in 25 patients. No deleterious germline mutation was identified in either group of patients. These results indicate that the CDKN2A/P16INK4A, P14ARF, CDK4 genes are not responsible for the vast majority of genetic susceptibility to uveal melanoma. They also suggest that one case of uveal melanoma in a family with a history of breast cancer is not sufficient to justify BRCA1/2 genetic testing when the classical criteria for molecular analysis are not present. International studies are ongoing in melanoma-prone families in an attempt to identify uveal melanoma susceptibility loci and genes.

Keywords

BRCA1 BRCA2 CDK4 CDKN2A genes Hereditary predisposition Uveal melanoma 

Copyright information

© Springer Science+Business Media B.V. 2010

Authors and Affiliations

  • B. Buecher
    • 1
  • M. Gauthier-Villars
    • 1
  • L. Desjardins
    • 2
  • L. Lumbroso-Le Rouic
    • 2
  • C. Levy
    • 2
  • A. De Pauw
    • 1
  • J. Bombled
    • 3
  • C. Tirapo
    • 1
  • C. Houdayer
    • 1
    • 4
  • B. Bressac-de Paillerets
    • 3
  • D. Stoppa-Lyonnet
    • 1
    • 4
  1. 1.Service de Génétique OncologiqueInstitut CurieParis Cedex 05France
  2. 2.Service d’Oncologie OphtalmologiqueInstitut CurieParis Cedex 05France
  3. 3.Service de GénétiqueInstitut de Cancérologie Gustave RoussyParis CedexFrance
  4. 4.Université Paris DescartesParisFrance

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