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IMPLICATIONS OF BAX, FAS, AND P53 IN THE PATHOGENESIS OF EARLY-STAGE MYCOSIS FUNGOIDES AND ALTERATIONS IN EXPRESSION FOLLOWING PHOTOCHEMOTHERAPY

BACKGROUND: The underlying molecular basis of mycosis fungoides (MF) has not yet been clarified. However, defects in apoptosis may contribute to its pathogenesis. AIM: We investigated the expression of Bax, Fas, and p53 in early-stage MF patients and any alterations in expression following photochem...

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Detalles Bibliográficos
Autores principales: Aydin, Fatma, Levent, Yildiz, Nilgun, Senturk, Pancar, Yuksel Esra, Yasar, Turanli Ahmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3221208/
https://www.ncbi.nlm.nih.gov/pubmed/22121263
http://dx.doi.org/10.4103/0019-5154.87130
Descripción
Sumario:BACKGROUND: The underlying molecular basis of mycosis fungoides (MF) has not yet been clarified. However, defects in apoptosis may contribute to its pathogenesis. AIM: We investigated the expression of Bax, Fas, and p53 in early-stage MF patients and any alterations in expression following photochemotherapy. MATERIALS AND METHODS: Bax, Fas, and p53 expressions were studied by immunohistochemistry in both keratinocytes and lymphocytes on paraffin-embedded skin specimens from 27 early-stage MF patients. RESULTS: Bax, Fas, and p53 staining was shown in the lymphocytes in 0/27, 26/27, and 11/27 patients at the time of diagnosis, whereas these ratios were 0/27, 9/27, and 0/27, respectively, after psoralen plus ultraviolet A (PUVA) treatment. The decrease in p53 and Fas expression in the lymphocytes was found statistically significant. Bax, Fas, and p53 staining in the keratinocytes was shown in 5/27, 27/27, and 25/27 patients at the time of diagnosis, whereas these ratios were 0/27, 22/27, and 4/27, respectively, after PUVA treatment. The decrease in p53, Fas, and Bax expression in the keratinocytes was found statistically significant. CONCLUSION: Although Bax seems unrelated with early-stage MF, Fas and p53 expression in the lymphocytes may contribute to the understanding of the pathogenesis of this disease.