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HGF/MET and the Immune System: Relevance for Cancer Immunotherapy

An overactivation of hepatocyte growth factor (HGF)/mesenchymal-epithelial transition factor (MET) axis promotes tumorigenesis and tumor progression in various cancer types. Research data recently evidenced that HGF/MET signaling is also involved also in the immune response, mainly modulating dendri...

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Autores principales: Papaccio, Federica, Della Corte, Carminia Maria, Viscardi, Giuseppe, Di Liello, Raimondo, Esposito, Giovanna, Sparano, Francesca, Ciardiello, Fortunato, Morgillo, Floriana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274701/
https://www.ncbi.nlm.nih.gov/pubmed/30441809
http://dx.doi.org/10.3390/ijms19113595
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author Papaccio, Federica
Della Corte, Carminia Maria
Viscardi, Giuseppe
Di Liello, Raimondo
Esposito, Giovanna
Sparano, Francesca
Ciardiello, Fortunato
Morgillo, Floriana
author_facet Papaccio, Federica
Della Corte, Carminia Maria
Viscardi, Giuseppe
Di Liello, Raimondo
Esposito, Giovanna
Sparano, Francesca
Ciardiello, Fortunato
Morgillo, Floriana
author_sort Papaccio, Federica
collection PubMed
description An overactivation of hepatocyte growth factor (HGF)/mesenchymal-epithelial transition factor (MET) axis promotes tumorigenesis and tumor progression in various cancer types. Research data recently evidenced that HGF/MET signaling is also involved also in the immune response, mainly modulating dendritic cells functions. In general, the pathway seems to play an immunosuppressive role, thus hypothesizing that it could constitute a mechanism of primary and acquired resistance to cancer immunotherapy. Recently, some approaches are being developed, including drug design and cell therapy to combine MET and programmed cell death receptor-1 (PD-1)/programmed cell death receptor-ligand 1 (PD-L1) inhibition. This approach could represent a new weapon in cancer therapy in the future.
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spelling pubmed-62747012018-12-15 HGF/MET and the Immune System: Relevance for Cancer Immunotherapy Papaccio, Federica Della Corte, Carminia Maria Viscardi, Giuseppe Di Liello, Raimondo Esposito, Giovanna Sparano, Francesca Ciardiello, Fortunato Morgillo, Floriana Int J Mol Sci Review An overactivation of hepatocyte growth factor (HGF)/mesenchymal-epithelial transition factor (MET) axis promotes tumorigenesis and tumor progression in various cancer types. Research data recently evidenced that HGF/MET signaling is also involved also in the immune response, mainly modulating dendritic cells functions. In general, the pathway seems to play an immunosuppressive role, thus hypothesizing that it could constitute a mechanism of primary and acquired resistance to cancer immunotherapy. Recently, some approaches are being developed, including drug design and cell therapy to combine MET and programmed cell death receptor-1 (PD-1)/programmed cell death receptor-ligand 1 (PD-L1) inhibition. This approach could represent a new weapon in cancer therapy in the future. MDPI 2018-11-14 /pmc/articles/PMC6274701/ /pubmed/30441809 http://dx.doi.org/10.3390/ijms19113595 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Papaccio, Federica
Della Corte, Carminia Maria
Viscardi, Giuseppe
Di Liello, Raimondo
Esposito, Giovanna
Sparano, Francesca
Ciardiello, Fortunato
Morgillo, Floriana
HGF/MET and the Immune System: Relevance for Cancer Immunotherapy
title HGF/MET and the Immune System: Relevance for Cancer Immunotherapy
title_full HGF/MET and the Immune System: Relevance for Cancer Immunotherapy
title_fullStr HGF/MET and the Immune System: Relevance for Cancer Immunotherapy
title_full_unstemmed HGF/MET and the Immune System: Relevance for Cancer Immunotherapy
title_short HGF/MET and the Immune System: Relevance for Cancer Immunotherapy
title_sort hgf/met and the immune system: relevance for cancer immunotherapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274701/
https://www.ncbi.nlm.nih.gov/pubmed/30441809
http://dx.doi.org/10.3390/ijms19113595
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