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The immune checkpoint VISTA is associated with prognosis in patients with malignant uveal melanoma

INTRODUCTION: Uveal melanoma (UM) is a rare yet deadly tumor. It is known for its high metastatic potential, which makes it one of the most aggressive and lethal cancers. Recently, immune checkpoints such as Programmed cell Death protein-1 (PD1) and Cytotoxic T-Lymphocyte-Associated significantly in...

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Autores principales: Issam Salah, Nour el Imane, Marnissi, Farida, Lakhdar, Abdelhakim, Karkouri, Mehdi, ElBelhadji, Mohamed, Badou, Abdallah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471992/
https://www.ncbi.nlm.nih.gov/pubmed/37662962
http://dx.doi.org/10.3389/fimmu.2023.1225140
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author Issam Salah, Nour el Imane
Marnissi, Farida
Lakhdar, Abdelhakim
Karkouri, Mehdi
ElBelhadji, Mohamed
Badou, Abdallah
author_facet Issam Salah, Nour el Imane
Marnissi, Farida
Lakhdar, Abdelhakim
Karkouri, Mehdi
ElBelhadji, Mohamed
Badou, Abdallah
author_sort Issam Salah, Nour el Imane
collection PubMed
description INTRODUCTION: Uveal melanoma (UM) is a rare yet deadly tumor. It is known for its high metastatic potential, which makes it one of the most aggressive and lethal cancers. Recently, immune checkpoints such as Programmed cell Death protein-1 (PD1) and Cytotoxic T-Lymphocyte-Associated significantly increasing patient survival in multiple human cancers, especially cutaneous melanoma. However, patients with UMs were excluded from these studies because of their molecular characteristics, which tend to be widely different from those of cutaneous melanoma. This study aimed to analyze the expression of V domain Ig Suppressor T-cell Activation (VISTA), a novel immune checkpoint, to evaluate its prognosis significance and its correlation with PD1 and CTLA-4. METHODS: Evaluation of VISTA, CTLA-4, and PD1 expression was performed through TCGA database analysis and immunohistochemistry using two independent cohorts with primary malignant UM. RESULTS AND DISCUSSION: Our results showed that VISTA expression was associated with tumor aggressiveness, T cell exhaustion, and the shortest median overall survival among patients. Surprisingly, PD1 protein expression was negative in all patients, whereas CTLA-4 expression was high in patients with advanced stages. Our findings suggest that VISTA may be a prognostic marker and an attractive treatment strategy for immunotherapy in patients with UM. Exploring its expression profile may predict response to immunotherapy and may lead to the improvement of precision therapy in malignant uveal melanoma patients.
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spelling pubmed-104719922023-09-02 The immune checkpoint VISTA is associated with prognosis in patients with malignant uveal melanoma Issam Salah, Nour el Imane Marnissi, Farida Lakhdar, Abdelhakim Karkouri, Mehdi ElBelhadji, Mohamed Badou, Abdallah Front Immunol Immunology INTRODUCTION: Uveal melanoma (UM) is a rare yet deadly tumor. It is known for its high metastatic potential, which makes it one of the most aggressive and lethal cancers. Recently, immune checkpoints such as Programmed cell Death protein-1 (PD1) and Cytotoxic T-Lymphocyte-Associated significantly increasing patient survival in multiple human cancers, especially cutaneous melanoma. However, patients with UMs were excluded from these studies because of their molecular characteristics, which tend to be widely different from those of cutaneous melanoma. This study aimed to analyze the expression of V domain Ig Suppressor T-cell Activation (VISTA), a novel immune checkpoint, to evaluate its prognosis significance and its correlation with PD1 and CTLA-4. METHODS: Evaluation of VISTA, CTLA-4, and PD1 expression was performed through TCGA database analysis and immunohistochemistry using two independent cohorts with primary malignant UM. RESULTS AND DISCUSSION: Our results showed that VISTA expression was associated with tumor aggressiveness, T cell exhaustion, and the shortest median overall survival among patients. Surprisingly, PD1 protein expression was negative in all patients, whereas CTLA-4 expression was high in patients with advanced stages. Our findings suggest that VISTA may be a prognostic marker and an attractive treatment strategy for immunotherapy in patients with UM. Exploring its expression profile may predict response to immunotherapy and may lead to the improvement of precision therapy in malignant uveal melanoma patients. Frontiers Media S.A. 2023-08-18 /pmc/articles/PMC10471992/ /pubmed/37662962 http://dx.doi.org/10.3389/fimmu.2023.1225140 Text en Copyright © 2023 Issam Salah, Marnissi, Lakhdar, Karkouri, ElBelhadji and Badou https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Issam Salah, Nour el Imane
Marnissi, Farida
Lakhdar, Abdelhakim
Karkouri, Mehdi
ElBelhadji, Mohamed
Badou, Abdallah
The immune checkpoint VISTA is associated with prognosis in patients with malignant uveal melanoma
title The immune checkpoint VISTA is associated with prognosis in patients with malignant uveal melanoma
title_full The immune checkpoint VISTA is associated with prognosis in patients with malignant uveal melanoma
title_fullStr The immune checkpoint VISTA is associated with prognosis in patients with malignant uveal melanoma
title_full_unstemmed The immune checkpoint VISTA is associated with prognosis in patients with malignant uveal melanoma
title_short The immune checkpoint VISTA is associated with prognosis in patients with malignant uveal melanoma
title_sort immune checkpoint vista is associated with prognosis in patients with malignant uveal melanoma
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471992/
https://www.ncbi.nlm.nih.gov/pubmed/37662962
http://dx.doi.org/10.3389/fimmu.2023.1225140
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