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Immunosurveillance of cancer cell stress

Cancer development is tightly controlled by effector immune responses that recognize and eliminate malignantly transformed cells. Nonetheless, certain immune subsets, such as tumor-associated macrophages, have been described to promote tumor growth, unraveling a double-edge role of the immune system...

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Autores principales: Lorenzo-Herrero, Seila, Sordo-Bahamonde, Christian, González, Segundo, López-Soto, Alejandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732214/
https://www.ncbi.nlm.nih.gov/pubmed/31535086
http://dx.doi.org/10.15698/cst2019.09.198
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author Lorenzo-Herrero, Seila
Sordo-Bahamonde, Christian
González, Segundo
López-Soto, Alejandro
author_facet Lorenzo-Herrero, Seila
Sordo-Bahamonde, Christian
González, Segundo
López-Soto, Alejandro
author_sort Lorenzo-Herrero, Seila
collection PubMed
description Cancer development is tightly controlled by effector immune responses that recognize and eliminate malignantly transformed cells. Nonetheless, certain immune subsets, such as tumor-associated macrophages, have been described to promote tumor growth, unraveling a double-edge role of the immune system in cancer. Cell stress can modulate the crosstalk between immune cells and tumor cells, reshaping tumor immunogenicity and/or immune function and phenotype. Infiltrating immune cells are exposed to the challenging conditions typically present in the tumor microenvironment. In return, the myriad of signaling pathways activated in response to stress conditions may tip the balance toward stimulation of antitumor responses or immune-mediated tumor progression. Here, we explore how distinct situations of cellular stress influence innate and adaptive immunity and the consequent impact on cancer establishment and progression.
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spelling pubmed-67322142019-09-18 Immunosurveillance of cancer cell stress Lorenzo-Herrero, Seila Sordo-Bahamonde, Christian González, Segundo López-Soto, Alejandro Cell Stress Review Cancer development is tightly controlled by effector immune responses that recognize and eliminate malignantly transformed cells. Nonetheless, certain immune subsets, such as tumor-associated macrophages, have been described to promote tumor growth, unraveling a double-edge role of the immune system in cancer. Cell stress can modulate the crosstalk between immune cells and tumor cells, reshaping tumor immunogenicity and/or immune function and phenotype. Infiltrating immune cells are exposed to the challenging conditions typically present in the tumor microenvironment. In return, the myriad of signaling pathways activated in response to stress conditions may tip the balance toward stimulation of antitumor responses or immune-mediated tumor progression. Here, we explore how distinct situations of cellular stress influence innate and adaptive immunity and the consequent impact on cancer establishment and progression. Shared Science Publishers OG 2019-07-03 /pmc/articles/PMC6732214/ /pubmed/31535086 http://dx.doi.org/10.15698/cst2019.09.198 Text en Copyright: © 2019 Lorenzo-Herrero et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.
spellingShingle Review
Lorenzo-Herrero, Seila
Sordo-Bahamonde, Christian
González, Segundo
López-Soto, Alejandro
Immunosurveillance of cancer cell stress
title Immunosurveillance of cancer cell stress
title_full Immunosurveillance of cancer cell stress
title_fullStr Immunosurveillance of cancer cell stress
title_full_unstemmed Immunosurveillance of cancer cell stress
title_short Immunosurveillance of cancer cell stress
title_sort immunosurveillance of cancer cell stress
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732214/
https://www.ncbi.nlm.nih.gov/pubmed/31535086
http://dx.doi.org/10.15698/cst2019.09.198
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