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Expression and prognostic value of putative cancer stem cell markers CD117 and CD15 in choroidal and ciliary body melanoma
  1. Adrian Lukenda1,
  2. Snjezana Dotlic2,
  3. Nenad Vukojevic3,
  4. Borna Saric4,
  5. Semir Vranic5,
  6. Kamelija Zarkovic6
  1. 1Ocna poliklinika Opto Centar, Zagreb, Croatia
  2. 2Department of Pathology and Cytology, University Hospital Center Zagreb, Zagreb, Croatia
  3. 3Department of Ophthalmology, University Hospital Center Zagreb, Zagreb, Croatia
  4. 4Ophthalmology Clinic, University Hospital “Sveti Duh”, Zagreb, Croatia
  5. 5Department of Pathology, Clinical Center of the University of Sarajevo, Sarajevo, Bosnia and Herzegovina
  6. 6Department of Pathology, Zagreb University School of Medicine, Zagreb, Croatia
  1. Correspondence to Dr Adrian Lukenda, Ocna poliklinika Opto Centar, Vlaska 64, Livadiceva 33, Zagreb 10000, Croatia; alukenda{at}opto-centar.hr

Abstract

Aims The aim of the present study was to immunohistochemically investigate the expression and prognostic significance of putative cancer stem cell markers CD117 (c-kit), CD34, CD20 and CD15 in a cohort of patients with primary choroidal and ciliary body melanoma.

Methods The immunohistochemical expression of these markers was evaluated using 3,3′-diaminobenzidine tetrahydrochloride (DAB) and 3-amino-9-ethylcarbazole (AEC) chromogens on paraffin-embedded tissue samples from 40 patients who underwent enucleation in the period from 1985 through 2000. Thirty-one patients had adequate tissue specimens for the analysis.

Results CD117 overexpression was observed in 12 of the 31 samples (39%) when AEC chromogen was used and in 14 of 26 (54%) samples when DAB was used. CD15 positivity was seen in three out of 30 (10%) samples with AEC and in six out of 26 (23%) samples with DAB. CD20 and CD34 exhibited no positivity in the tested samples. During the average follow-up time of 8.7 years (range 0.5–22 years), 17 patients (55%) died due to metastatic disease. The Kaplan–Meier plots showed a significantly shorter overall and disease-free survival in CD117-positive patients when the AEC chromogen was used. CD15 expression was not associated with patients’ survival. In multivariate analysis, patients expressing the CD117 AEC had 4.13 times higher risk of lethal outcome in comparison with CD117 AEC negative patients.

Conclusions Our retrospective cohort study has for the first time demonstrated a small proportion of CD15-positive uveal melanomas. CD117 AEC overexpression was associated with a worse outcome in patients with choroidal and ciliary body melanoma. Further studies should confirm the validity of these observations and their potential for targeted treatment modalities.

  • IMMUNOHISTOCHEMISTRY
  • MELANOMA
  • EYE
  • c-kit expression

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