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A promising antitumor method: Targeting CSC with immune cells modified with CAR
Tumors pose a great threat to human health; as a subgroup of tumor cells, cancer stem cells (CSCs) contribute to the genesis, development, metastasis, and recurrence of tumors because of their enhanced proliferation and multidirectional differentiation. Thus, a critical step in tumor treatment is to...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403009/ https://www.ncbi.nlm.nih.gov/pubmed/36032145 http://dx.doi.org/10.3389/fimmu.2022.937327 |
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author | Huang, Binjie Miao, Lele Liu, Jie Zhang, Jiaxing Li, Yumin |
author_facet | Huang, Binjie Miao, Lele Liu, Jie Zhang, Jiaxing Li, Yumin |
author_sort | Huang, Binjie |
collection | PubMed |
description | Tumors pose a great threat to human health; as a subgroup of tumor cells, cancer stem cells (CSCs) contribute to the genesis, development, metastasis, and recurrence of tumors because of their enhanced proliferation and multidirectional differentiation. Thus, a critical step in tumor treatment is to inhibit CSCs. Researchers have proposed many methods to inhibit or reduce CSCs, including monoclonal antibodies targeting specific surface molecules of CSCs, signal pathway inhibitors, and energy metabolic enzyme inhibitors and inducing differentiation therapy. Additionally, immunotherapy with immune cells engineered with a chimeric antigen receptor (CAR) showed favorable results. However, there are few comprehensive reviews in this area. In this review, we summarize the recent CSC targets used for CSC inhibition and the different immune effector cells (T cells, natural killer (NK) cells, and macrophages) which are engineered with CAR used for CSC therapy. Finally, we list the main challenges and options in targeting CSC with CAR-based immunotherapy. The design targeting two tumor antigens (one CSC antigen and one mature common tumor antigen) should be more reasonable and practical; meanwhile, we highlight the potential of CAR-NK in tumor treatment. |
format | Online Article Text |
id | pubmed-9403009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94030092022-08-26 A promising antitumor method: Targeting CSC with immune cells modified with CAR Huang, Binjie Miao, Lele Liu, Jie Zhang, Jiaxing Li, Yumin Front Immunol Immunology Tumors pose a great threat to human health; as a subgroup of tumor cells, cancer stem cells (CSCs) contribute to the genesis, development, metastasis, and recurrence of tumors because of their enhanced proliferation and multidirectional differentiation. Thus, a critical step in tumor treatment is to inhibit CSCs. Researchers have proposed many methods to inhibit or reduce CSCs, including monoclonal antibodies targeting specific surface molecules of CSCs, signal pathway inhibitors, and energy metabolic enzyme inhibitors and inducing differentiation therapy. Additionally, immunotherapy with immune cells engineered with a chimeric antigen receptor (CAR) showed favorable results. However, there are few comprehensive reviews in this area. In this review, we summarize the recent CSC targets used for CSC inhibition and the different immune effector cells (T cells, natural killer (NK) cells, and macrophages) which are engineered with CAR used for CSC therapy. Finally, we list the main challenges and options in targeting CSC with CAR-based immunotherapy. The design targeting two tumor antigens (one CSC antigen and one mature common tumor antigen) should be more reasonable and practical; meanwhile, we highlight the potential of CAR-NK in tumor treatment. Frontiers Media S.A. 2022-08-11 /pmc/articles/PMC9403009/ /pubmed/36032145 http://dx.doi.org/10.3389/fimmu.2022.937327 Text en Copyright © 2022 Huang, Miao, Liu, Zhang and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Huang, Binjie Miao, Lele Liu, Jie Zhang, Jiaxing Li, Yumin A promising antitumor method: Targeting CSC with immune cells modified with CAR |
title | A promising antitumor method: Targeting CSC with immune cells modified with CAR |
title_full | A promising antitumor method: Targeting CSC with immune cells modified with CAR |
title_fullStr | A promising antitumor method: Targeting CSC with immune cells modified with CAR |
title_full_unstemmed | A promising antitumor method: Targeting CSC with immune cells modified with CAR |
title_short | A promising antitumor method: Targeting CSC with immune cells modified with CAR |
title_sort | promising antitumor method: targeting csc with immune cells modified with car |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403009/ https://www.ncbi.nlm.nih.gov/pubmed/36032145 http://dx.doi.org/10.3389/fimmu.2022.937327 |
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