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EPHA2, EPHA4, and EPHA6 Expression in Uveal Melanomas: Searching for the Culprits of Neoplasia

Authors :
Alexandros Pergaris
Eugene Danas
Pawel Gajdzis
Georgia Levidou
Malgorzata Gajdzis
Nathalie Cassoux
Sophie Gardrat
Piotr Donizy
Penelope Korkolopoulou
Nikolaos Kavantzas
Jerzy Klijanienko
Stamatios Theocharis
Source :
Diagnostics; Volume 12; Issue 5; Pages: 1025
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

Uveal melanomas (UMs) comprise the most common primary intraocular malignancies in adults, with the eye representing the second most common site for melanoma, following the skin. Prognosis remains poor, with approximately half of the cases presenting with metastatic disease at the time of diagnosis. Erythropoietin-producing human hepatocellular receptors (EPHs) comprise the largest known family of tyrosine receptors, in which, along with their ligands, ephrins, play an important role in a plethora of processes in human physiology, and are implicated in key steps of carcinogenesis. In the present study, EPHA2, EPHA4, and EPHA6 immunohistochemical expressions were investigated in UM tissues and further correlated to a multitude of clinicopathological parameters, including disease stage and patients’ overall survival (OS). High levels of EPHA2 expression were significantly associated with increased tumor vertical thickness (p = 0.03) and the presence of intrascleral involvement (p = 0.05), whereas high EPHA6 nuclear expression was associated with older age at diagnosis (p = 0.03) and absence of retinal detachment (p = 0.05). In a multivariate survival analysis, increased EPHA4 expression was associated with shortened OS along with the presence of metastasis (p < 0.001) and monosomy 3 (p = 0.02). In a separate model, the concurrent overexpression of at least two of the investigated EPHs (HR = 14.7, p = 0.03) also proved to be an independent poor prognostic factor. In conclusion, our results implicate these specific members of the EPHA group as potential biomarkers for disease prognosis as well as possible targets for the development of novel therapeutic interventions.

Details

ISSN :
20754418
Volume :
12
Database :
OpenAIRE
Journal :
Diagnostics
Accession number :
edsair.doi.dedup.....233273c3f43009fe149be20e47ecd185
Full Text :
https://doi.org/10.3390/diagnostics12051025