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Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer
Monoclonal antibodies (mAbs) are used as targeted therapies against cancers. These mAbs kill cancer cells via various mechanisms of actions. In this study, human embryonic stem cells (hESCs) was used as the immunogen to generate a panel of antibodies. From this panel of mAbs, A19 was found to bind b...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072701/ https://www.ncbi.nlm.nih.gov/pubmed/30072783 http://dx.doi.org/10.1038/s41598-018-30070-z |
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author | Tan, Heng Liang Yong, Charlene Tan, Bao Zhu Fong, Wey Jia Padmanabhan, Jayanthi Chin, Angela Ding, Vanessa Lau, Ally Zheng, Lu Bi, Xuezhi Yang, Yuansheng Choo, Andre |
author_facet | Tan, Heng Liang Yong, Charlene Tan, Bao Zhu Fong, Wey Jia Padmanabhan, Jayanthi Chin, Angela Ding, Vanessa Lau, Ally Zheng, Lu Bi, Xuezhi Yang, Yuansheng Choo, Andre |
author_sort | Tan, Heng Liang |
collection | PubMed |
description | Monoclonal antibodies (mAbs) are used as targeted therapies against cancers. These mAbs kill cancer cells via various mechanisms of actions. In this study, human embryonic stem cells (hESCs) was used as the immunogen to generate a panel of antibodies. From this panel of mAbs, A19 was found to bind both hESC and various cancer cell lines. The antigen target of A19 was identified as Erbb-2 and glycan analysis showed that A19 binds to a N-glycan epitope on the antigen. A19 was elucidated to internalize into cancer cells following binding to Erbb-2 and hence developed as an antibody-drug conjugate (ADC). Using ADC as the mechanism of action, A19 was able to kill cancer cells in vitro and delayed the onset of tumour formation in mice xenograft model. When compared to Herceptin, A19 binds to different isoforms of Erbb-2 and does not compete with Herceptin for the same epitope. Hence, A19 has the potential to be developed as an alternative targeted therapeutic agent for cancers expressing Erbb-2. |
format | Online Article Text |
id | pubmed-6072701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60727012018-08-06 Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer Tan, Heng Liang Yong, Charlene Tan, Bao Zhu Fong, Wey Jia Padmanabhan, Jayanthi Chin, Angela Ding, Vanessa Lau, Ally Zheng, Lu Bi, Xuezhi Yang, Yuansheng Choo, Andre Sci Rep Article Monoclonal antibodies (mAbs) are used as targeted therapies against cancers. These mAbs kill cancer cells via various mechanisms of actions. In this study, human embryonic stem cells (hESCs) was used as the immunogen to generate a panel of antibodies. From this panel of mAbs, A19 was found to bind both hESC and various cancer cell lines. The antigen target of A19 was identified as Erbb-2 and glycan analysis showed that A19 binds to a N-glycan epitope on the antigen. A19 was elucidated to internalize into cancer cells following binding to Erbb-2 and hence developed as an antibody-drug conjugate (ADC). Using ADC as the mechanism of action, A19 was able to kill cancer cells in vitro and delayed the onset of tumour formation in mice xenograft model. When compared to Herceptin, A19 binds to different isoforms of Erbb-2 and does not compete with Herceptin for the same epitope. Hence, A19 has the potential to be developed as an alternative targeted therapeutic agent for cancers expressing Erbb-2. Nature Publishing Group UK 2018-08-02 /pmc/articles/PMC6072701/ /pubmed/30072783 http://dx.doi.org/10.1038/s41598-018-30070-z Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tan, Heng Liang Yong, Charlene Tan, Bao Zhu Fong, Wey Jia Padmanabhan, Jayanthi Chin, Angela Ding, Vanessa Lau, Ally Zheng, Lu Bi, Xuezhi Yang, Yuansheng Choo, Andre Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer |
title | Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer |
title_full | Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer |
title_fullStr | Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer |
title_full_unstemmed | Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer |
title_short | Conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer |
title_sort | conservation of oncofetal antigens on human embryonic stem cells enables discovery of monoclonal antibodies against cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6072701/ https://www.ncbi.nlm.nih.gov/pubmed/30072783 http://dx.doi.org/10.1038/s41598-018-30070-z |
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