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Reduced Expression of Autotaxin Predicts Survival in Uveal Melanoma
  1. Arun D. Singh (singha{at}ccf.org),
  2. Karen Sisley,
  3. Yaomin Xu,
  4. Jianbo Li,
  5. Pieter Faber,
  6. Sarah J. Plummer,
  7. Hardeep S. Mudhar,
  8. Ian G. Rennie,
  9. Patricia M. Kessler,
  10. Graham Casey,
  11. Bryan G. Williams
  1. Cole Eye Institute, Cleveland Clinic Foundation, United States
  2. Royal Hallamshire Hospital, Sheffield, United Kingdom
  3. Quantitative Health Sciences Cleveland Clinic Foundation, United States
  4. Quantitative Health Sciences Cleveland Clinic Foundation, United States
  5. Cancer Biology, Cleveland Clinic Foundation, United States
  6. Cancer Biology, Cleveland Clinic Foundation, United States
  7. Royal Hallamshire Hospital, Sheffield, United Kingdom
  8. Royal Hallamshire Hospital, Sheffield, United Kingdom
  9. Cancer Biology, Cleveland Clinic Foundation, United States
  10. Cancer Biology, Cleveland Clinic Foundation, United States
  11. Monash Institute of Medical Research, Monash University, Melbourne, Australia, Australia

    Abstract

    Aim: In an effort to identify patients with uveal melanoma at high risk of metastasis, we under took correlation of gene expression profiles with histopathology data and tumour-related mortality.

    Methods: The RNA was isolated from 27 samples of uveal melanoma from patients who had consented to undergo enucleation and transcripts profiled using a cDNA array comprised of sequence-verified cDNA clones representing approximately 4,000 genes implicated in cancer development. Two multivariate data mining techniques, Hierarchical cluster analysis and Multidimensional scaling, were used to investigate the grouping structure in the gene expression data. Cluster analysis was performed with 10,000 randomly selected subset of genes and the cumulative contribution of all the genes in making the correct grouping were recorded.

    Results: Hierarchical cluster analysis and Multidimensional scaling revealed two distinct classes. When correlated with the data on metastasis, the two molecular classes corresponded very well to the survival data for the 27 patients. Thirty two discrete genes (corresponding to 44 probe sets) that correctly defined the molecular classes were selected. A single gene (ectonucleotide pyrophosphatase/phosphodiesterase 2; autotaxin) could classify the molecular classes. The expression pattern was confirmed using real time quantitative PCR.

    Conclusions: Gene expression profiling identifies two distinct prognostic classes of uveal melanoma. Underexpression of Autotaxin in class 2 uveal melanoma with a poor prognosis needs to be explored further.

    • autotoxin
    • gene expression
    • metastasis
    • survival
    • uveal melanoma

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