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Mitochondrial Proteins as Source of Cancer Neoantigens

In the past decade, anti-tumour immune responses have been successfully exploited to improve the outcome of patients with different cancers. Significant progress has been made in taking advantage of different types of T cell functions for therapeutic purposes. Despite these achievements, only a subs...

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Detalles Bibliográficos
Autores principales: Prota, Gennaro, Lechuga-Vieco, Ana Victoria, De Libero, Gennaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8909979/
https://www.ncbi.nlm.nih.gov/pubmed/35269772
http://dx.doi.org/10.3390/ijms23052627
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author Prota, Gennaro
Lechuga-Vieco, Ana Victoria
De Libero, Gennaro
author_facet Prota, Gennaro
Lechuga-Vieco, Ana Victoria
De Libero, Gennaro
author_sort Prota, Gennaro
collection PubMed
description In the past decade, anti-tumour immune responses have been successfully exploited to improve the outcome of patients with different cancers. Significant progress has been made in taking advantage of different types of T cell functions for therapeutic purposes. Despite these achievements, only a subset of patients respond favorably to immunotherapy. Therefore, there is a need of novel approaches to improve the effector functions of immune cells and to recognize the major targets of anti-tumour immunity. A major hallmark of cancer is metabolic rewiring associated with switch of mitochondrial functions. These changes are a consequence of high energy demand and increased macromolecular synthesis in cancer cells. Such adaptations in tumour cells might generate novel targets of tumour therapy, including the generation of neoantigens. Here, we review the most recent advances in research on the immune response to mitochondrial proteins in different cellular conditions.
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spelling pubmed-89099792022-03-11 Mitochondrial Proteins as Source of Cancer Neoantigens Prota, Gennaro Lechuga-Vieco, Ana Victoria De Libero, Gennaro Int J Mol Sci Review In the past decade, anti-tumour immune responses have been successfully exploited to improve the outcome of patients with different cancers. Significant progress has been made in taking advantage of different types of T cell functions for therapeutic purposes. Despite these achievements, only a subset of patients respond favorably to immunotherapy. Therefore, there is a need of novel approaches to improve the effector functions of immune cells and to recognize the major targets of anti-tumour immunity. A major hallmark of cancer is metabolic rewiring associated with switch of mitochondrial functions. These changes are a consequence of high energy demand and increased macromolecular synthesis in cancer cells. Such adaptations in tumour cells might generate novel targets of tumour therapy, including the generation of neoantigens. Here, we review the most recent advances in research on the immune response to mitochondrial proteins in different cellular conditions. MDPI 2022-02-27 /pmc/articles/PMC8909979/ /pubmed/35269772 http://dx.doi.org/10.3390/ijms23052627 Text en © 2022 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
Prota, Gennaro
Lechuga-Vieco, Ana Victoria
De Libero, Gennaro
Mitochondrial Proteins as Source of Cancer Neoantigens
title Mitochondrial Proteins as Source of Cancer Neoantigens
title_full Mitochondrial Proteins as Source of Cancer Neoantigens
title_fullStr Mitochondrial Proteins as Source of Cancer Neoantigens
title_full_unstemmed Mitochondrial Proteins as Source of Cancer Neoantigens
title_short Mitochondrial Proteins as Source of Cancer Neoantigens
title_sort mitochondrial proteins as source of cancer neoantigens
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8909979/
https://www.ncbi.nlm.nih.gov/pubmed/35269772
http://dx.doi.org/10.3390/ijms23052627
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