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Development of a new EGFR antibody antagonist which exhibits potential biological effects against laryngeal cancer
BACKGROUND: Laryngeal cancer is a common malignant tumor of the head and neck. Clinical treatment methods mainly include radiotherapy and chemotherapy, but the toxicity and side effects of these treatments seriously affect the quality of life of patients. Currently, there are no specific anti-laryng...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267258/ https://www.ncbi.nlm.nih.gov/pubmed/34277764 http://dx.doi.org/10.21037/atm-21-1839 |
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author | Ren, Kai Wang, Binquan Qi, Qingyan |
author_facet | Ren, Kai Wang, Binquan Qi, Qingyan |
author_sort | Ren, Kai |
collection | PubMed |
description | BACKGROUND: Laryngeal cancer is a common malignant tumor of the head and neck. Clinical treatment methods mainly include radiotherapy and chemotherapy, but the toxicity and side effects of these treatments seriously affect the quality of life of patients. Currently, there are no specific anti-laryngeal cancer drugs available. Therefore, it is necessary to develop new targeted drugs for laryngeal cancer. METHODS: We established a cell model of laryngeal cancer in vitro and a TU686 xenograft model in vivo. We then carried out the related research through a series of experiments [including laser confocal microscopy, enzyme linked immune sorbent assay (ELISA) and Western blot]. RESULTS: The results showed that the epidermal growth factor receptor (EGFR) antibody antagonist 6E-C could not only specifically bind to EGFR, but also specifically inhibit the binding of EGF to EGFR. Further analysis indicated that 6E-C could inhibit the EGFR-mediated intracellular signaling pathway. Furthermore, 6E-C inhibited xenograft tumor growth in vivo. CONCLUSIONS: In summary, we have successfully prepared a new anti-EGFR antibody antagonist, which exhibited anti-laryngeal cancer effects in vitro and in vivo. The current research demonstrates that the EGFR antibody antagonist 6E-C shows potential as an effective anti-laryngeal cancer agent, with potential clinical application value. This study therefore provides a solid foundation for related research in the future. |
format | Online Article Text |
id | pubmed-8267258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-82672582021-07-16 Development of a new EGFR antibody antagonist which exhibits potential biological effects against laryngeal cancer Ren, Kai Wang, Binquan Qi, Qingyan Ann Transl Med Original Article BACKGROUND: Laryngeal cancer is a common malignant tumor of the head and neck. Clinical treatment methods mainly include radiotherapy and chemotherapy, but the toxicity and side effects of these treatments seriously affect the quality of life of patients. Currently, there are no specific anti-laryngeal cancer drugs available. Therefore, it is necessary to develop new targeted drugs for laryngeal cancer. METHODS: We established a cell model of laryngeal cancer in vitro and a TU686 xenograft model in vivo. We then carried out the related research through a series of experiments [including laser confocal microscopy, enzyme linked immune sorbent assay (ELISA) and Western blot]. RESULTS: The results showed that the epidermal growth factor receptor (EGFR) antibody antagonist 6E-C could not only specifically bind to EGFR, but also specifically inhibit the binding of EGF to EGFR. Further analysis indicated that 6E-C could inhibit the EGFR-mediated intracellular signaling pathway. Furthermore, 6E-C inhibited xenograft tumor growth in vivo. CONCLUSIONS: In summary, we have successfully prepared a new anti-EGFR antibody antagonist, which exhibited anti-laryngeal cancer effects in vitro and in vivo. The current research demonstrates that the EGFR antibody antagonist 6E-C shows potential as an effective anti-laryngeal cancer agent, with potential clinical application value. This study therefore provides a solid foundation for related research in the future. AME Publishing Company 2021-06 /pmc/articles/PMC8267258/ /pubmed/34277764 http://dx.doi.org/10.21037/atm-21-1839 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Ren, Kai Wang, Binquan Qi, Qingyan Development of a new EGFR antibody antagonist which exhibits potential biological effects against laryngeal cancer |
title | Development of a new EGFR antibody antagonist which exhibits potential biological effects against laryngeal cancer |
title_full | Development of a new EGFR antibody antagonist which exhibits potential biological effects against laryngeal cancer |
title_fullStr | Development of a new EGFR antibody antagonist which exhibits potential biological effects against laryngeal cancer |
title_full_unstemmed | Development of a new EGFR antibody antagonist which exhibits potential biological effects against laryngeal cancer |
title_short | Development of a new EGFR antibody antagonist which exhibits potential biological effects against laryngeal cancer |
title_sort | development of a new egfr antibody antagonist which exhibits potential biological effects against laryngeal cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8267258/ https://www.ncbi.nlm.nih.gov/pubmed/34277764 http://dx.doi.org/10.21037/atm-21-1839 |
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