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 inJournal of dermatological science Vol. 64; no. 3; pp. 185 - 190
Main Authors Valencak, Julia, Schmid, Katharina, Trautinger, Franz, Wallnöfer, Werner, Muellauer, Leonhard, Soleiman, Afschin, Knobler, Robert, Haitel, Andrea, Pehamberger, Hubert, Raderer, Markus
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ireland Ltd 01.12.2011
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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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ISSN:0923-1811
1873-569X
DOI:10.1016/j.jdermsci.2011.08.011