| Literature DB >> 32556361 |
Lihi Atzmony1, Lilach Moyal, Meora Feinmesser, Batya Gorovitz, Avraham Hirshberg, Iris Amitay-Laish, Hadas Prag-Naveh, Aviv Barzilai, Emmilia Hodak.
Abstract
Recent studies suggest that folliculotropic mycosis fungoides (FMF), the most common variant of mycosis fungoides (MF), presents with 2 distinct clinicopathological stages: early indolent stage and more aggressive advanced/tumour stage. To further characterize these stages, miR-155 expression was studied with qRT-PCR and found to be significantly higher in biopsies of tumour-stage FMF compared with early-stage FMF and inflammatory dermatoses. There was no statistically significant difference in miR-155 expression between early-stage FMF and early-stage MF, nor between tumour-stage FMF and tumour-stage MF. Immunohistochemical analysis revealed a significantly increased number of dermal Ki-67+ proliferating lymphocytes in tumour-stage FMF, together with an increased number of CD20+ B cells and CD68+ macrophages compared with early-stage FMF. Thus, similar to classic MF, miR-155, Ki-67 tumour cell immunoreactivity, and certain tumour-infiltrating inflammatory cells are differentially expressed in early- vs tumour-stage FMF. The results of this study corroborate the notion that FMF presents with 2 distinct stages.Entities:
Keywords: Ki-67; cutaneous T-cell lymphoma; microenvironment; stage, microRNA-155; folliculotropic mycosis fungoides
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Year: 2020 PMID: 32556361 PMCID: PMC9207631 DOI: 10.2340/00015555-3578
Source DB: PubMed Journal: Acta Derm Venereol ISSN: 0001-5555 Impact factor: 3.875