1. Cyclo-oxygenase-2 expression in photon-radiated and non-radiated uveal melanomas
- Author
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Daniela Suesskind, Frank Paulsen, Karl U. Bartz-Schmidt, Jens Martin Rohrbach, Bernhard Spitzer, Martin S. Spitzer, and Markus Buchgeister
- Subjects
Adult ,Male ,Uveal Neoplasms ,Pathology ,medicine.medical_specialty ,Adolescent ,Proliferative index ,medicine.medical_treatment ,Uveal Neoplasm ,Metastasis ,Immunoenzyme Techniques ,Radiotherapy, High-Energy ,In Situ Nick-End Labeling ,Adjuvant therapy ,medicine ,Humans ,Melanoma ,Aged ,Aged, 80 and over ,Photons ,business.industry ,General Medicine ,Middle Aged ,Uvea ,Prognosis ,medicine.disease ,Radiation therapy ,Ophthalmology ,Ki-67 Antigen ,medicine.anatomical_structure ,Cyclooxygenase 2 ,Immunohistochemistry ,Female ,Ruthenium Radioisotopes ,business - Abstract
Purpose: To determine and compare cyclo-oxygenase-2 (COX-2) expression in photon-radiated and non-radiated malignant uveal melanomas and to analyse the correlation between COX-2 expression and prognosis. Methods: Immunohistochemical staining for COX-2 was performed on 21 uveal melanomas that were endoresected after prior stereotactic radiotherapy with photons and on 22 tumours that were treated by endoresection without prior radiotherapy. COX-2 staining was further analysed in respect to cell type, maximal prominence, time interval between radiotherapy and surgery, apoptotic index (AI), proliferative index (PI) and the development of metastatic disease. Results: There was no difference in COX-2 expression between radiated and non-radiated melanomas (P > 0.15). COX-2 staining correlated with neither the tumour prominence (P > 0.40) nor the AI or the PI (both P > 0.35). Tumours with high COX-2 expression were significantly more likely to develop metastasis (P = 0.022). Conclusion: Radiotherapy with photons does not induce COX-2 expression in malignant melanomas of the uvea. But high COX-2 expression may be a marker for poor prognosis.
- Published
- 2009
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