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Monoclonal antibodies and chimeric antigen receptor (CAR) T cells in the treatment of colorectal cancer
Colorectal cancer (CRC) is the third most common cancer and the second leading cause of cancer deaths worldwide. Besides common therapeutic approaches, such as surgery, chemotherapy, and radiotherapy, novel therapeutic approaches, including immunotherapy, have been an advent in CRC treatment. The im...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851946/ https://www.ncbi.nlm.nih.gov/pubmed/33522929 http://dx.doi.org/10.1186/s12935-021-01763-9 |
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author | Jin, Ke-Tao Chen, Bo Liu, Yu-Yao Lan, H uan-Rong Yan, Jie-Ping |
author_facet | Jin, Ke-Tao Chen, Bo Liu, Yu-Yao Lan, H uan-Rong Yan, Jie-Ping |
author_sort | Jin, Ke-Tao |
collection | PubMed |
description | Colorectal cancer (CRC) is the third most common cancer and the second leading cause of cancer deaths worldwide. Besides common therapeutic approaches, such as surgery, chemotherapy, and radiotherapy, novel therapeutic approaches, including immunotherapy, have been an advent in CRC treatment. The immunotherapy approaches try to elicit patients` immune responses against tumor cells to eradicate the tumor. Monoclonal antibodies (mAbs) and chimeric antigen receptor (CAR) T cells are two branches of cancer immunotherapy. MAbs demonstrate the great ability to completely recognize cancer cell-surface receptors and blockade proliferative or inhibitory pathways. On the other hand, T cell activation by genetically engineered CAR receptor via the TCR/CD3 and costimulatory domains can induce potent immune responses against specific tumor-associated antigens (TAAs). Both of these approaches have beneficial anti-tumor effects on CRC. Herein, we review the different mAbs against various pathways and their applications in clinical trials, the different types of CAR-T cells, various specific CAR-T cells against TAAs, and their clinical use in CRC treatment. |
format | Online Article Text |
id | pubmed-7851946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78519462021-02-03 Monoclonal antibodies and chimeric antigen receptor (CAR) T cells in the treatment of colorectal cancer Jin, Ke-Tao Chen, Bo Liu, Yu-Yao Lan, H uan-Rong Yan, Jie-Ping Cancer Cell Int Review Colorectal cancer (CRC) is the third most common cancer and the second leading cause of cancer deaths worldwide. Besides common therapeutic approaches, such as surgery, chemotherapy, and radiotherapy, novel therapeutic approaches, including immunotherapy, have been an advent in CRC treatment. The immunotherapy approaches try to elicit patients` immune responses against tumor cells to eradicate the tumor. Monoclonal antibodies (mAbs) and chimeric antigen receptor (CAR) T cells are two branches of cancer immunotherapy. MAbs demonstrate the great ability to completely recognize cancer cell-surface receptors and blockade proliferative or inhibitory pathways. On the other hand, T cell activation by genetically engineered CAR receptor via the TCR/CD3 and costimulatory domains can induce potent immune responses against specific tumor-associated antigens (TAAs). Both of these approaches have beneficial anti-tumor effects on CRC. Herein, we review the different mAbs against various pathways and their applications in clinical trials, the different types of CAR-T cells, various specific CAR-T cells against TAAs, and their clinical use in CRC treatment. BioMed Central 2021-02-01 /pmc/articles/PMC7851946/ /pubmed/33522929 http://dx.doi.org/10.1186/s12935-021-01763-9 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Jin, Ke-Tao Chen, Bo Liu, Yu-Yao Lan, H uan-Rong Yan, Jie-Ping Monoclonal antibodies and chimeric antigen receptor (CAR) T cells in the treatment of colorectal cancer |
title | Monoclonal antibodies and chimeric antigen receptor (CAR) T cells in the treatment of colorectal cancer |
title_full | Monoclonal antibodies and chimeric antigen receptor (CAR) T cells in the treatment of colorectal cancer |
title_fullStr | Monoclonal antibodies and chimeric antigen receptor (CAR) T cells in the treatment of colorectal cancer |
title_full_unstemmed | Monoclonal antibodies and chimeric antigen receptor (CAR) T cells in the treatment of colorectal cancer |
title_short | Monoclonal antibodies and chimeric antigen receptor (CAR) T cells in the treatment of colorectal cancer |
title_sort | monoclonal antibodies and chimeric antigen receptor (car) t cells in the treatment of colorectal cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851946/ https://www.ncbi.nlm.nih.gov/pubmed/33522929 http://dx.doi.org/10.1186/s12935-021-01763-9 |
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