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Conjunctival melanoma copy number alterations and correlation with mutation status, tumor features and clinical outcome

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  • Nihal Kenawy
  • Helen Kalirai
  • Joseph J Sacco
  • Sarah L Lake
  • Steffen Heegaard
  • Ann-Cathrine Larsen
  • Paul T Finger
  • Tatyana Milman
  • Kimberly Chin
  • Carlo Mosci
  • Francesco Lanza
  • Alexandre Moulin
  • Caroline A Schmitt
  • Jean Pierre Caujolle
  • Célia Maschi
  • Marina Marinkovic
  • Azzam F Taktak
  • Heinrich Heimann
  • Bertil E Damato
  • Sarah E Coupland
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Relatively little is known about the genetic aberrations of conjunctival melanomas (CoM) and their correlation with clinical and histomorphological features as well as prognosis. The aim of this large collaborative multicenter study was to determine potential key biomarkers for metastatic risk and any druggable targets for high metastatic risk CoM. Using Affymetrix single nucleotide polymorphism genotyping arrays on 59 CoM, we detected frequent amplifications on chromosome (chr) 6p and deletions on 7q, and characterized mutation-specific copy number alterations. Deletions on chr 10q11.21-26.2, a region harboring the tumor suppressor genes, PDCD4, SUFU, NEURL1, PTEN, RASSF4, DMBT1, and C10orf90 and C10orf99, significantly correlated with metastasis (Fisher's exact, p ≤ 0.04), lymphatic invasion (Fisher's exact, p ≤ 0.02), increasing tumor thickness (Mann–Whitney, p ≤ 0.02), and BRAF mutation (Fisher's exact, p ≤ 0.05). This enhanced insight into CoM biology is a step toward identifying patients at risk of metastasis and potential therapeutic targets for systemic disease.

Original languageEnglish
JournalPigment Cell & Melanoma Research
Volume32
Issue number4
Pages (from-to)564-575
Number of pages12
ISSN1755-1471
DOIs
Publication statusPublished - 2019

Bibliographical note

© 2019 The Authors. Pigment Cell & Melanoma Research Published by John Wiley & Sons Ltd.

    Research areas

  • allele-specific copy number, BRAF/NRAS mutation, conjunctival melanoma, copy number alteration, metastasis

ID: 56583366