Cargando…

H(2)Mab-19, an anti-human epidermal growth factor receptor 2 monoclonal antibody exerts antitumor activity in mouse oral cancer xenografts

Human epidermal growth factor receptor 2 (HER2) is reported to be overexpressed in breast cancers and is associated with poor clinical outcome. Trastuzumab is a humanized anti-HER2 antibody that offers significant survival benefits to patients with HER2-overexpressing breast cancer. In this study, a...

Descripción completa

Detalles Bibliográficos
Autores principales: Takei, Junko, Kaneko, Mika Kato, Ohishi, Tomokazu, Kawada, Manabu, Harada, Hiroyuki, Kato, Yukinari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388441/
https://www.ncbi.nlm.nih.gov/pubmed/32765652
http://dx.doi.org/10.3892/etm.2020.8765
_version_ 1783564310534946816
author Takei, Junko
Kaneko, Mika Kato
Ohishi, Tomokazu
Kawada, Manabu
Harada, Hiroyuki
Kato, Yukinari
author_facet Takei, Junko
Kaneko, Mika Kato
Ohishi, Tomokazu
Kawada, Manabu
Harada, Hiroyuki
Kato, Yukinari
author_sort Takei, Junko
collection PubMed
description Human epidermal growth factor receptor 2 (HER2) is reported to be overexpressed in breast cancers and is associated with poor clinical outcome. Trastuzumab is a humanized anti-HER2 antibody that offers significant survival benefits to patients with HER2-overexpressing breast cancer. In this study, a novel anti-HER2 monoclonal antibody (mAb), H(2)Mab-19 (IgG(2b), kappa) was developed. Antibody-dependent cellular cytotoxicity (ADCC), complement-dependent cytotoxicity (CDC), and antitumor activity of H(2)Mab-19 were investigated using both breast cancer and oral cancer cell lines. H(2)Mab-19 demonstrated cytotoxicity in BT-474 (a human breast cancer cell line) and HSC-2 or SAS (human oral cancer cell lines). H(2)Mab-19 also possessed both ADCC and CDC activity against BT-474, HSC-2, and SAS cell lines. In comparison to control mouse IgG, H(2)Mab-19 significantly reduced tumor development in BT-474, HSC-2, and SAS xenografts. Collectively, these results suggest that treatment with H(2)Mab-19 may be a useful therapy for patients with HER2-expressing breast and oral cancers.
format Online
Article
Text
id pubmed-7388441
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-73884412020-08-05 H(2)Mab-19, an anti-human epidermal growth factor receptor 2 monoclonal antibody exerts antitumor activity in mouse oral cancer xenografts Takei, Junko Kaneko, Mika Kato Ohishi, Tomokazu Kawada, Manabu Harada, Hiroyuki Kato, Yukinari Exp Ther Med Articles Human epidermal growth factor receptor 2 (HER2) is reported to be overexpressed in breast cancers and is associated with poor clinical outcome. Trastuzumab is a humanized anti-HER2 antibody that offers significant survival benefits to patients with HER2-overexpressing breast cancer. In this study, a novel anti-HER2 monoclonal antibody (mAb), H(2)Mab-19 (IgG(2b), kappa) was developed. Antibody-dependent cellular cytotoxicity (ADCC), complement-dependent cytotoxicity (CDC), and antitumor activity of H(2)Mab-19 were investigated using both breast cancer and oral cancer cell lines. H(2)Mab-19 demonstrated cytotoxicity in BT-474 (a human breast cancer cell line) and HSC-2 or SAS (human oral cancer cell lines). H(2)Mab-19 also possessed both ADCC and CDC activity against BT-474, HSC-2, and SAS cell lines. In comparison to control mouse IgG, H(2)Mab-19 significantly reduced tumor development in BT-474, HSC-2, and SAS xenografts. Collectively, these results suggest that treatment with H(2)Mab-19 may be a useful therapy for patients with HER2-expressing breast and oral cancers. D.A. Spandidos 2020-08 2020-05-18 /pmc/articles/PMC7388441/ /pubmed/32765652 http://dx.doi.org/10.3892/etm.2020.8765 Text en Copyright: © Takei et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Articles
Takei, Junko
Kaneko, Mika Kato
Ohishi, Tomokazu
Kawada, Manabu
Harada, Hiroyuki
Kato, Yukinari
H(2)Mab-19, an anti-human epidermal growth factor receptor 2 monoclonal antibody exerts antitumor activity in mouse oral cancer xenografts
title H(2)Mab-19, an anti-human epidermal growth factor receptor 2 monoclonal antibody exerts antitumor activity in mouse oral cancer xenografts
title_full H(2)Mab-19, an anti-human epidermal growth factor receptor 2 monoclonal antibody exerts antitumor activity in mouse oral cancer xenografts
title_fullStr H(2)Mab-19, an anti-human epidermal growth factor receptor 2 monoclonal antibody exerts antitumor activity in mouse oral cancer xenografts
title_full_unstemmed H(2)Mab-19, an anti-human epidermal growth factor receptor 2 monoclonal antibody exerts antitumor activity in mouse oral cancer xenografts
title_short H(2)Mab-19, an anti-human epidermal growth factor receptor 2 monoclonal antibody exerts antitumor activity in mouse oral cancer xenografts
title_sort h(2)mab-19, an anti-human epidermal growth factor receptor 2 monoclonal antibody exerts antitumor activity in mouse oral cancer xenografts
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388441/
https://www.ncbi.nlm.nih.gov/pubmed/32765652
http://dx.doi.org/10.3892/etm.2020.8765
work_keys_str_mv AT takeijunko h2mab19anantihumanepidermalgrowthfactorreceptor2monoclonalantibodyexertsantitumoractivityinmouseoralcancerxenografts
AT kanekomikakato h2mab19anantihumanepidermalgrowthfactorreceptor2monoclonalantibodyexertsantitumoractivityinmouseoralcancerxenografts
AT ohishitomokazu h2mab19anantihumanepidermalgrowthfactorreceptor2monoclonalantibodyexertsantitumoractivityinmouseoralcancerxenografts
AT kawadamanabu h2mab19anantihumanepidermalgrowthfactorreceptor2monoclonalantibodyexertsantitumoractivityinmouseoralcancerxenografts
AT haradahiroyuki h2mab19anantihumanepidermalgrowthfactorreceptor2monoclonalantibodyexertsantitumoractivityinmouseoralcancerxenografts
AT katoyukinari h2mab19anantihumanepidermalgrowthfactorreceptor2monoclonalantibodyexertsantitumoractivityinmouseoralcancerxenografts