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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...

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Autores principales: Jin, Ke-Tao, Chen, Bo, Liu, Yu-Yao, Lan, H uan-Rong, Yan, Jie-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
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.
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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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