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MAGE-A1 in lung adenocarcinoma as a promising target of chimeric antigen receptor T cells
BACKGROUND: Cancer/testis antigens (CTAs) are a special type of tumor antigen and are believed to act as potential targets for cancer immunotherapy. METHODS: In this study, we first screened a rational CTA MAGE-A1 for lung adenocarcinoma (LUAD) and explored the detailed characteristics of MAGE-A1 in...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805483/ https://www.ncbi.nlm.nih.gov/pubmed/31640756 http://dx.doi.org/10.1186/s13045-019-0793-7 |
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author | Mao, Yuan Fan, Weifei Hu, Hao Zhang, Louqian Michel, Jerod Wu, Yaqin Wang, Jun Jia, Lizhou Tang, Xiaojun Xu, Li Chen, Yan Zhu, Jin Feng, Zhenqing Xu, Lin Yin, Rong Tang, Qi |
author_facet | Mao, Yuan Fan, Weifei Hu, Hao Zhang, Louqian Michel, Jerod Wu, Yaqin Wang, Jun Jia, Lizhou Tang, Xiaojun Xu, Li Chen, Yan Zhu, Jin Feng, Zhenqing Xu, Lin Yin, Rong Tang, Qi |
author_sort | Mao, Yuan |
collection | PubMed |
description | BACKGROUND: Cancer/testis antigens (CTAs) are a special type of tumor antigen and are believed to act as potential targets for cancer immunotherapy. METHODS: In this study, we first screened a rational CTA MAGE-A1 for lung adenocarcinoma (LUAD) and explored the detailed characteristics of MAGE-A1 in LUAD development through a series of phenotypic experiments. Then, we developed a novel MAGE-A1-CAR-T cell (mCART) using lentiviral vector based on our previous MAGE-A1-scFv. The anti-tumor effects of this mCART were finally investigated in vitro and in vivo. RESULTS: The results showed striking malignant behaviors of MAGE-A1 in LUAD development, which further validated the rationality of MAGE-A1 as an appropriate target for LUAD treatment. Then, the innovative mCART was successfully constructed, and mCART displayed encouraging tumor-inhibitory efficacy in LUAD cells and xenografts. CONCLUSIONS: Taken together, our data suggest that MAGE-A1 is a promising candidate marker for LUAD therapy and the MAGE-A1-specific CAR-T cell immunotherapy may be an effective strategy for the treatment of MAGE-A1-positive LUAD. |
format | Online Article Text |
id | pubmed-6805483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68054832019-10-24 MAGE-A1 in lung adenocarcinoma as a promising target of chimeric antigen receptor T cells Mao, Yuan Fan, Weifei Hu, Hao Zhang, Louqian Michel, Jerod Wu, Yaqin Wang, Jun Jia, Lizhou Tang, Xiaojun Xu, Li Chen, Yan Zhu, Jin Feng, Zhenqing Xu, Lin Yin, Rong Tang, Qi J Hematol Oncol Research BACKGROUND: Cancer/testis antigens (CTAs) are a special type of tumor antigen and are believed to act as potential targets for cancer immunotherapy. METHODS: In this study, we first screened a rational CTA MAGE-A1 for lung adenocarcinoma (LUAD) and explored the detailed characteristics of MAGE-A1 in LUAD development through a series of phenotypic experiments. Then, we developed a novel MAGE-A1-CAR-T cell (mCART) using lentiviral vector based on our previous MAGE-A1-scFv. The anti-tumor effects of this mCART were finally investigated in vitro and in vivo. RESULTS: The results showed striking malignant behaviors of MAGE-A1 in LUAD development, which further validated the rationality of MAGE-A1 as an appropriate target for LUAD treatment. Then, the innovative mCART was successfully constructed, and mCART displayed encouraging tumor-inhibitory efficacy in LUAD cells and xenografts. CONCLUSIONS: Taken together, our data suggest that MAGE-A1 is a promising candidate marker for LUAD therapy and the MAGE-A1-specific CAR-T cell immunotherapy may be an effective strategy for the treatment of MAGE-A1-positive LUAD. BioMed Central 2019-10-22 /pmc/articles/PMC6805483/ /pubmed/31640756 http://dx.doi.org/10.1186/s13045-019-0793-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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. |
spellingShingle | Research Mao, Yuan Fan, Weifei Hu, Hao Zhang, Louqian Michel, Jerod Wu, Yaqin Wang, Jun Jia, Lizhou Tang, Xiaojun Xu, Li Chen, Yan Zhu, Jin Feng, Zhenqing Xu, Lin Yin, Rong Tang, Qi MAGE-A1 in lung adenocarcinoma as a promising target of chimeric antigen receptor T cells |
title | MAGE-A1 in lung adenocarcinoma as a promising target of chimeric antigen receptor T cells |
title_full | MAGE-A1 in lung adenocarcinoma as a promising target of chimeric antigen receptor T cells |
title_fullStr | MAGE-A1 in lung adenocarcinoma as a promising target of chimeric antigen receptor T cells |
title_full_unstemmed | MAGE-A1 in lung adenocarcinoma as a promising target of chimeric antigen receptor T cells |
title_short | MAGE-A1 in lung adenocarcinoma as a promising target of chimeric antigen receptor T cells |
title_sort | mage-a1 in lung adenocarcinoma as a promising target of chimeric antigen receptor t cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805483/ https://www.ncbi.nlm.nih.gov/pubmed/31640756 http://dx.doi.org/10.1186/s13045-019-0793-7 |
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