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Survivin protein in UVB induced apoptosis of melanoma cells and in melanoma progression.
Linköping University, Faculty of Health Sciences. Linköping University, Department of Biomedicine and Surgery, Division of dermatology and venereology.
2005 (English)In: Oncology Reports, ISSN 1021-335X, Vol. 13, no 6, 1121-1126 p.Article in journal (Refereed) Published
Abstract [en]

A model system of cultivated melanoma cells and melanomas from patients were used in this study to clarify whether survivin protein was involved in UVB induced cell damage and in melanoma progression. The melanoma cells in culture were exposed to different doses of UVB and post-cultivated for various periods of time. Cell viability, apoptotic index and expression of survivin proteins were estimated. Expression of the survivin in normal tissue, nevi, primary and metastatic melanomas from the patients were also examined by immunohistochemistry. Results showed that UVB induced cell damage and apoptosis in melanoma cells. Primary and wt p53 cells were more sensitive than metastatic and mutant p53 melanoma cells. Expression of survivin protein was markedly decreased in the primary melanoma cells after exposure to UVB compared to the metastasis. The expression was markedly decreased in wt p53 melanoma cells, but not in the mutant p53 melanoma cells. Survivin protein was expressed in nevi, primary and metastatic melanomas. However, the normal tissues were not expressed in the survivin protein. Survivin plays an important role in UVB-induced apoptosis. Overexpression of survivin might be a biomarker for early diagnosis for melanoma.

Place, publisher, year, edition, pages
2005. Vol. 13, no 6, 1121-1126 p.
National Category
Medical and Health Sciences
URN: urn:nbn:se:liu:diva-31077Local ID: 16803OAI: diva2:251900
Available from: 2009-10-09 Created: 2009-10-09 Last updated: 2011-01-12

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Zhang, Hong
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