Differential Immunoexpression of BRAF/V600E, Senescence Markers, PTEN, and T-type Calcium Channels in Acquired Naevi According to their Histopathological and Dermoscopic Classification

4Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

BRAF/V600E mutation and other cell growth/growth-control mechanisms are involved in naevogenesis and melanomagenesis. Immunoexpression of BRAF/V600E and other molecules (p16, phosphatase and tensin homologue (PTEN), Ki67, hTERT and Cav3.1 and 3.2 calcium channels) were investigated in 80 histopatho-logically and dermoscopically classified acquired naevi. Regarding BRAF/V600E, dysplastic naevi showed lower immunostaining than common naevi, which was significant in comparison with intradermal nae-vi, which showed the highest BRAF/V600E histosco-re. Junctional naevi showed the lowest BRAF/V600E levels. Globular/cobblestone and reticular dermo-scopic patterns were consistently associated with high and low BRAF/V600E immunoexpression, respective-ly, but Zalaudek’s peripheral globule pattern (CR/PG) showed the highest BRAF/V600E immunoexpression. Among global patterns, the previously not investigated multicomponent pattern showed the lowest BRAF/ V600E immunoexpression. Regarding the remaining biomarkers, new immunohistochemical features were found, in particular p16 and PTEN low expression in multicomponent pattern; and Ki67, hTERT and Cav.3.1 high expression in CR/PG. In conclusion, histopatho-logy and dermoscopy provide complementary informa-tion regarding the biology of melanocytic naevi.

Cite

CITATION STYLE

APA

Moreno, S., Maiques, O., Barcelo, C., Romero, M., Santacana, M., Gomez, I., … Marti, R. M. (2021). Differential Immunoexpression of BRAF/V600E, Senescence Markers, PTEN, and T-type Calcium Channels in Acquired Naevi According to their Histopathological and Dermoscopic Classification. Acta Dermato-Venereologica, 101(11). https://doi.org/10.2340/ACTADV.V101.361

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free