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Gp-100 as a Novel Therapeutic Target in Uveal Melanoma
SIMPLE SUMMARY: Glycoprotein 100 (Gp-100) is a protein highly expressed in melanoma tissue that has recently been effectively targeted by tebentafusp, a first-in-class bispecific protein of the immune-mobilizing monoclonal T cell receptors against cancer (ImmTACs) family. Recently, a randomized phas...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8656894/ https://www.ncbi.nlm.nih.gov/pubmed/34885078 http://dx.doi.org/10.3390/cancers13235968 |
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author | Martinez-Perez, Daniel Viñal, David Solares, Isabel Espinosa, Enrique Feliu, Jaime |
author_facet | Martinez-Perez, Daniel Viñal, David Solares, Isabel Espinosa, Enrique Feliu, Jaime |
author_sort | Martinez-Perez, Daniel |
collection | PubMed |
description | SIMPLE SUMMARY: Glycoprotein 100 (Gp-100) is a protein highly expressed in melanoma tissue that has recently been effectively targeted by tebentafusp, a first-in-class bispecific protein of the immune-mobilizing monoclonal T cell receptors against cancer (ImmTACs) family. Recently, a randomized phase III trial reported an overall survival benefit for tebentafusp in patients with untreated metastatic uveal melanoma. ABSTRACT: Uveal melanoma is a rare neoplasm with poor prognosis in the metastatic setting. Unlike cutaneous melanoma, treatment with kinase inhibitors or immune checkpoint inhibitors is not effective. Glycoprotein 100 (Gp-100) is a protein highly expressed in melanocytes and melanoma that has recently been effectively targeted by tebentafusp, a first-in-class bispecific protein of the immune-mobilizing monoclonal T cell receptors against cancer (ImmTACs) family. Tebentafusp targets tumor cells that express a peptide of Gp-100 presented by HLA*A0201, creating an immune synapse that kills targeted tumor cells. Recently, a randomized phase III trial reported an overall survival benefit for tebentafusp in patients with untreated metastatic uveal melanoma. The aim of this comprehensive review is to summarize evidence of Gp-100 as a therapeutic target in melanoma, and the preclinical and clinical development of tebentafusp as a novel therapeutic strategy for patients with uveal melanoma. |
format | Online Article Text |
id | pubmed-8656894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86568942021-12-10 Gp-100 as a Novel Therapeutic Target in Uveal Melanoma Martinez-Perez, Daniel Viñal, David Solares, Isabel Espinosa, Enrique Feliu, Jaime Cancers (Basel) Review SIMPLE SUMMARY: Glycoprotein 100 (Gp-100) is a protein highly expressed in melanoma tissue that has recently been effectively targeted by tebentafusp, a first-in-class bispecific protein of the immune-mobilizing monoclonal T cell receptors against cancer (ImmTACs) family. Recently, a randomized phase III trial reported an overall survival benefit for tebentafusp in patients with untreated metastatic uveal melanoma. ABSTRACT: Uveal melanoma is a rare neoplasm with poor prognosis in the metastatic setting. Unlike cutaneous melanoma, treatment with kinase inhibitors or immune checkpoint inhibitors is not effective. Glycoprotein 100 (Gp-100) is a protein highly expressed in melanocytes and melanoma that has recently been effectively targeted by tebentafusp, a first-in-class bispecific protein of the immune-mobilizing monoclonal T cell receptors against cancer (ImmTACs) family. Tebentafusp targets tumor cells that express a peptide of Gp-100 presented by HLA*A0201, creating an immune synapse that kills targeted tumor cells. Recently, a randomized phase III trial reported an overall survival benefit for tebentafusp in patients with untreated metastatic uveal melanoma. The aim of this comprehensive review is to summarize evidence of Gp-100 as a therapeutic target in melanoma, and the preclinical and clinical development of tebentafusp as a novel therapeutic strategy for patients with uveal melanoma. MDPI 2021-11-27 /pmc/articles/PMC8656894/ /pubmed/34885078 http://dx.doi.org/10.3390/cancers13235968 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Martinez-Perez, Daniel Viñal, David Solares, Isabel Espinosa, Enrique Feliu, Jaime Gp-100 as a Novel Therapeutic Target in Uveal Melanoma |
title | Gp-100 as a Novel Therapeutic Target in Uveal Melanoma |
title_full | Gp-100 as a Novel Therapeutic Target in Uveal Melanoma |
title_fullStr | Gp-100 as a Novel Therapeutic Target in Uveal Melanoma |
title_full_unstemmed | Gp-100 as a Novel Therapeutic Target in Uveal Melanoma |
title_short | Gp-100 as a Novel Therapeutic Target in Uveal Melanoma |
title_sort | gp-100 as a novel therapeutic target in uveal melanoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8656894/ https://www.ncbi.nlm.nih.gov/pubmed/34885078 http://dx.doi.org/10.3390/cancers13235968 |
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