High expression of Dicer reveals a negative prognostic influence in certain subtypes of primary cutaneous T cell lymphomas
Abstract Background Aberrant expression of microRNAs (miRNAs) has been implicated in oncogenesis of various tumors and primary cutaneous T cell lymphomas. Dicer, a ribonuclease III-like enzyme is essential for miRNA processing. Objective We initiated a retrospective study to characterize the alterat...
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Published in | Journal of dermatological science Vol. 64; no. 3; pp. 185 - 190 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Ireland Ltd
01.12.2011
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Subjects | |
Online Access | Get full text |
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Summary: | Abstract Background Aberrant expression of microRNAs (miRNAs) has been implicated in oncogenesis of various tumors and primary cutaneous T cell lymphomas. Dicer, a ribonuclease III-like enzyme is essential for miRNA processing. Objective We initiated a retrospective study to characterize the alterations in the expression profile of Dicer in patients with primary cutaneous T cell lymphomas (CTCL). Methods A total of 50 consecutive patients with primary CTCL were studied, with the majority having mycosis fungoides ( n = 34). Five patients had primary cutaneous CD 30+ anaplastic large cell lymphoma, four patients each had lymphomatoid papulosis and primary cutaneous CD4-positive small/medium T-cell lymphoma, one primary cutaneous γδ T cell lymphoma, one Sézary syndrome and another subcutaneous panniculitis-like T cell lymphoma of αβ-phenotype. Immunohistochemistry was performed on paraffin sections using a commercially available antibody against Dicer. Intensity of expression was correlated with clinical parameters including disease specific survival (DSS) and time to progression (TTP). Results After a median follow-up of 74 months (range: 1–271), 12/50 patients (24%) have died. Univariate and multivariate analysis for disease-specific survival showed Dicer expression and stage as a negative predictive factor in the sole group of MF patients ( n = 34) as well as in the heterogeneous group of patients ( n = 50), but not gender, histological subtype, primary localization of disease, age and recurrence of lymphoma ( p > 0.05). Conclusion Our data suggest Dicer expression as a possible molecular marker in patients with MF and apparently indicate that miRNA(s) might be of clinical relevance in CTCL. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0923-1811 1873-569X |
DOI: | 10.1016/j.jdermsci.2011.08.011 |