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Immune evasion by cancer stem cells

Tumor immunity represents a new avenue for cancer therapy. Immune checkpoint inhibitors have successfully improved outcomes in several tumor types. In addition, currently, immune cell-based therapy is also attracting significant attention. However, the clinical efficacy of these treatments requires...

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Detalles Bibliográficos
Autores principales: Tsuchiya, Hiroyuki, Shiota, Goshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966825/
https://www.ncbi.nlm.nih.gov/pubmed/33778133
http://dx.doi.org/10.1016/j.reth.2021.02.006
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author Tsuchiya, Hiroyuki
Shiota, Goshi
author_facet Tsuchiya, Hiroyuki
Shiota, Goshi
author_sort Tsuchiya, Hiroyuki
collection PubMed
description Tumor immunity represents a new avenue for cancer therapy. Immune checkpoint inhibitors have successfully improved outcomes in several tumor types. In addition, currently, immune cell-based therapy is also attracting significant attention. However, the clinical efficacy of these treatments requires further improvement. The mechanisms through which cancer cells escape the immune response must be identified and clarified. Cancer stem cells (CSCs) play a central role in multiple aspects of malignant tumors. CSCs can initiate tumors in partially immunocompromised mice, whereas non-CSCs fail to form tumors, suggesting that tumor initiation is a definitive function of CSCs. However, the fact that non-CSCs also initiate tumors in more highly immunocompromised mice suggests that the immune evasion property may be a more fundamental feature of CSCs rather than a tumor-initiating property. In this review, we summarize studies that have elucidated how CSCs evade tumor immunity and create an immunosuppressive milieu with a focus on CSC-specific characteristics and functions. These profound mechanisms provide important clues for the development of novel tumor immunotherapies.
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spelling pubmed-79668252021-03-25 Immune evasion by cancer stem cells Tsuchiya, Hiroyuki Shiota, Goshi Regen Ther Review Tumor immunity represents a new avenue for cancer therapy. Immune checkpoint inhibitors have successfully improved outcomes in several tumor types. In addition, currently, immune cell-based therapy is also attracting significant attention. However, the clinical efficacy of these treatments requires further improvement. The mechanisms through which cancer cells escape the immune response must be identified and clarified. Cancer stem cells (CSCs) play a central role in multiple aspects of malignant tumors. CSCs can initiate tumors in partially immunocompromised mice, whereas non-CSCs fail to form tumors, suggesting that tumor initiation is a definitive function of CSCs. However, the fact that non-CSCs also initiate tumors in more highly immunocompromised mice suggests that the immune evasion property may be a more fundamental feature of CSCs rather than a tumor-initiating property. In this review, we summarize studies that have elucidated how CSCs evade tumor immunity and create an immunosuppressive milieu with a focus on CSC-specific characteristics and functions. These profound mechanisms provide important clues for the development of novel tumor immunotherapies. Japanese Society for Regenerative Medicine 2021-03-11 /pmc/articles/PMC7966825/ /pubmed/33778133 http://dx.doi.org/10.1016/j.reth.2021.02.006 Text en © 2021 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Tsuchiya, Hiroyuki
Shiota, Goshi
Immune evasion by cancer stem cells
title Immune evasion by cancer stem cells
title_full Immune evasion by cancer stem cells
title_fullStr Immune evasion by cancer stem cells
title_full_unstemmed Immune evasion by cancer stem cells
title_short Immune evasion by cancer stem cells
title_sort immune evasion by cancer stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966825/
https://www.ncbi.nlm.nih.gov/pubmed/33778133
http://dx.doi.org/10.1016/j.reth.2021.02.006
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