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A novel monoclonal antibody associated with glucoside kills gastric adenocarcinoma AGS cells based on glycosylation target
Glycosylation results in the production of glycans which are required for certain proteins to function. These glycans are also present on cell surfaces where they help maintain cell membrane integrity and are a key component of immune recognition. As such, cancer has been shown to alter glycosylatio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9465190/ https://www.ncbi.nlm.nih.gov/pubmed/35946053 http://dx.doi.org/10.1111/jcmm.17504 |
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author | Xu, Heng Dun, Boying Liu, Beiyi Mysona, David She, Jin‐Xiong Ma, Rong |
author_facet | Xu, Heng Dun, Boying Liu, Beiyi Mysona, David She, Jin‐Xiong Ma, Rong |
author_sort | Xu, Heng |
collection | PubMed |
description | Glycosylation results in the production of glycans which are required for certain proteins to function. These glycans are also present on cell surfaces where they help maintain cell membrane integrity and are a key component of immune recognition. As such, cancer has been shown to alter glycosylation to promote tumour proliferation, invasion, angiogenesis, and immune envasion. Currently, there are few therapeutic monoclonal antibodies (mAb) which target glycosylation alterations in cancer. Here, we report a novel mAb associated with a glucoside, mAb 201E4, which is able induce cancer cell death and apoptosis based on a specific glycosylation target. This mAb evokes cancer cell death in vitro via caspase, fas, and mitochondrial associated apoptotic pathways. The efficacy of this mAb was further confirmed in vivo as treatment of mice with mAb 201E4 resulted in potent tumour shrinkage. Finally, the antibody was proven to be specific to glycosylation alterations in cancer and have no binding to normal tissues. This data indicates that mAb 201E4 successfully targets glycosylation alterations in neoplasms to induce cancer cell death, which may provide a new strategy for therapy in cancer. |
format | Online Article Text |
id | pubmed-9465190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94651902022-09-14 A novel monoclonal antibody associated with glucoside kills gastric adenocarcinoma AGS cells based on glycosylation target Xu, Heng Dun, Boying Liu, Beiyi Mysona, David She, Jin‐Xiong Ma, Rong J Cell Mol Med Original Articles Glycosylation results in the production of glycans which are required for certain proteins to function. These glycans are also present on cell surfaces where they help maintain cell membrane integrity and are a key component of immune recognition. As such, cancer has been shown to alter glycosylation to promote tumour proliferation, invasion, angiogenesis, and immune envasion. Currently, there are few therapeutic monoclonal antibodies (mAb) which target glycosylation alterations in cancer. Here, we report a novel mAb associated with a glucoside, mAb 201E4, which is able induce cancer cell death and apoptosis based on a specific glycosylation target. This mAb evokes cancer cell death in vitro via caspase, fas, and mitochondrial associated apoptotic pathways. The efficacy of this mAb was further confirmed in vivo as treatment of mice with mAb 201E4 resulted in potent tumour shrinkage. Finally, the antibody was proven to be specific to glycosylation alterations in cancer and have no binding to normal tissues. This data indicates that mAb 201E4 successfully targets glycosylation alterations in neoplasms to induce cancer cell death, which may provide a new strategy for therapy in cancer. John Wiley and Sons Inc. 2022-08-09 2022-09 /pmc/articles/PMC9465190/ /pubmed/35946053 http://dx.doi.org/10.1111/jcmm.17504 Text en © 2022 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Xu, Heng Dun, Boying Liu, Beiyi Mysona, David She, Jin‐Xiong Ma, Rong A novel monoclonal antibody associated with glucoside kills gastric adenocarcinoma AGS cells based on glycosylation target |
title | A novel monoclonal antibody associated with glucoside kills gastric adenocarcinoma AGS cells based on glycosylation target |
title_full | A novel monoclonal antibody associated with glucoside kills gastric adenocarcinoma AGS cells based on glycosylation target |
title_fullStr | A novel monoclonal antibody associated with glucoside kills gastric adenocarcinoma AGS cells based on glycosylation target |
title_full_unstemmed | A novel monoclonal antibody associated with glucoside kills gastric adenocarcinoma AGS cells based on glycosylation target |
title_short | A novel monoclonal antibody associated with glucoside kills gastric adenocarcinoma AGS cells based on glycosylation target |
title_sort | novel monoclonal antibody associated with glucoside kills gastric adenocarcinoma ags cells based on glycosylation target |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9465190/ https://www.ncbi.nlm.nih.gov/pubmed/35946053 http://dx.doi.org/10.1111/jcmm.17504 |
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