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Ann Diagn Pathol ; 72: 152332, 2024 Oct.
Article in English | MEDLINE | ID: mdl-38776734

ABSTRACT

Tubulin ß-3 staining pattern and staining intensity of 5-hydroxymethyl cytosine (5-hmC) are potential diagnostic and prognostic markers in melanocytic lesions that need further evaluation. Melanocytic nevi and primary cutaneous melanomas were immunohistochemically stained for tubulin-ß-3 and 5-hmC. Immunoreactivity and staining patterns were correlated with Breslow-thickness, clinical and pathological characteristics, and progression-free survival. Melanocytes showed positive tubulin ß-3 staining. However, in most nevi, tubulin ß-3 staining appeared as a gradient with intense cytoplasmic staining in cells of the superficial part of the lesion that faded to weak staining in the deep dermal part, while no gradient was found in deep penetrating nevi and melanomas. In 53 % of the melanomas, areas with loss of tubulin ß-3 staining were found. 5-hmC staining intensity was significantly higher in melanocytic nevi compared to melanomas. Breslow thickness in combination with low 5-hmC score and loss of tubulin-ß-3 staining was predictive for poor prognosis. As single markers, tubulin-ß-3 and 5-hmC can be useful to distinguish between melanocytic nevi and melanoma, but staining variability limits the use of 5-hmC. In melanomas measuring >1.5 mm, combination of low 5-hmC score and loss of tubulin-ß-3 staining may have prognostic value.


Subject(s)
5-Methylcytosine , Biomarkers, Tumor , Melanoma , Skin Neoplasms , Tubulin , Humans , Melanoma/diagnosis , Melanoma/metabolism , Melanoma/pathology , Biomarkers, Tumor/metabolism , Biomarkers, Tumor/analysis , Prognosis , Male , Female , Tubulin/metabolism , Tubulin/analysis , Skin Neoplasms/diagnosis , Skin Neoplasms/pathology , Skin Neoplasms/metabolism , Middle Aged , 5-Methylcytosine/analogs & derivatives , 5-Methylcytosine/metabolism , 5-Methylcytosine/analysis , Aged , Adult , Immunohistochemistry/methods , Nevus, Pigmented/diagnosis , Nevus, Pigmented/pathology , Nevus, Pigmented/metabolism , Melanoma, Cutaneous Malignant , Aged, 80 and over , Melanocytes/pathology , Melanocytes/metabolism
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