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An anti-TROP2 monoclonal antibody TrMab-6 exerts antitumor activity in breast cancer mouse xenograft models

Trophoblast cell surface antigen 2 (TROP2), reported to be overexpressed in several types of cancer, is involved in cell proliferation, invasion, metastasis, and poor prognosis of many types of cancer. Previously, a highly sensitive anti-TROP2 monoclonal antibody (clone TrMab-6; mouse IgG(2b), κ) wa...

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Autores principales: Tanaka, Tomohiro, Ohishi, Tomokazu, Asano, Teizo, Takei, Junko, Nanamiya, Ren, Hosono, Hideki, Sano, Masato, Harada, Hiroyuki, Kawada, Manabu, Kaneko, Mika K., Kato, Yukinari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144932/
https://www.ncbi.nlm.nih.gov/pubmed/34013368
http://dx.doi.org/10.3892/or.2021.8083
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author Tanaka, Tomohiro
Ohishi, Tomokazu
Asano, Teizo
Takei, Junko
Nanamiya, Ren
Hosono, Hideki
Sano, Masato
Harada, Hiroyuki
Kawada, Manabu
Kaneko, Mika K.
Kato, Yukinari
author_facet Tanaka, Tomohiro
Ohishi, Tomokazu
Asano, Teizo
Takei, Junko
Nanamiya, Ren
Hosono, Hideki
Sano, Masato
Harada, Hiroyuki
Kawada, Manabu
Kaneko, Mika K.
Kato, Yukinari
author_sort Tanaka, Tomohiro
collection PubMed
description Trophoblast cell surface antigen 2 (TROP2), reported to be overexpressed in several types of cancer, is involved in cell proliferation, invasion, metastasis, and poor prognosis of many types of cancer. Previously, a highly sensitive anti-TROP2 monoclonal antibody (clone TrMab-6; mouse IgG(2b), κ) was developed using a Cell-Based Immunization and Screening (CBIS) method. TrMab-6 was useful for investigations using flow cytometry, western blot, and immunohistochemistry. The aim of the present study was to investigate whether TrMab-6 possesses in vitro antibody-dependent cellular cytotoxicity (ADCC) or complement-dependent cytotoxicity (CDC) activities or in vivo antitumor activities using mouse xenograft models of TROP2-overexpressed CHO-K1 (CHO/TROP2) and breast cancer cell lines, including MCF7, MDA-MB-231, and MDA-MB-468. In vitro experiments revealed that TrMab-6 strongly induced ADCC and CDC activities against CHO/TROP2 and the three breast cancer cell lines, whereas it did not show those activities against parental CHO-K1 and MCF7/TROP2-knockout cells. Furthermore, in vivo experiments on CHO/TROP2 and MCF7 ×enografts revealed that TrMab-6 significantly reduced tumor growth, whereas it did not show antitumor activities against parental CHO-K1 and MCF7/TROP2-knockout xenografts. The findings suggest that TrMab-6 is a promising treatment option for TROP2-expressing breast cancers.
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spelling pubmed-81449322021-05-28 An anti-TROP2 monoclonal antibody TrMab-6 exerts antitumor activity in breast cancer mouse xenograft models Tanaka, Tomohiro Ohishi, Tomokazu Asano, Teizo Takei, Junko Nanamiya, Ren Hosono, Hideki Sano, Masato Harada, Hiroyuki Kawada, Manabu Kaneko, Mika K. Kato, Yukinari Oncol Rep Articles Trophoblast cell surface antigen 2 (TROP2), reported to be overexpressed in several types of cancer, is involved in cell proliferation, invasion, metastasis, and poor prognosis of many types of cancer. Previously, a highly sensitive anti-TROP2 monoclonal antibody (clone TrMab-6; mouse IgG(2b), κ) was developed using a Cell-Based Immunization and Screening (CBIS) method. TrMab-6 was useful for investigations using flow cytometry, western blot, and immunohistochemistry. The aim of the present study was to investigate whether TrMab-6 possesses in vitro antibody-dependent cellular cytotoxicity (ADCC) or complement-dependent cytotoxicity (CDC) activities or in vivo antitumor activities using mouse xenograft models of TROP2-overexpressed CHO-K1 (CHO/TROP2) and breast cancer cell lines, including MCF7, MDA-MB-231, and MDA-MB-468. In vitro experiments revealed that TrMab-6 strongly induced ADCC and CDC activities against CHO/TROP2 and the three breast cancer cell lines, whereas it did not show those activities against parental CHO-K1 and MCF7/TROP2-knockout cells. Furthermore, in vivo experiments on CHO/TROP2 and MCF7 ×enografts revealed that TrMab-6 significantly reduced tumor growth, whereas it did not show antitumor activities against parental CHO-K1 and MCF7/TROP2-knockout xenografts. The findings suggest that TrMab-6 is a promising treatment option for TROP2-expressing breast cancers. D.A. Spandidos 2021-07 2021-05-19 /pmc/articles/PMC8144932/ /pubmed/34013368 http://dx.doi.org/10.3892/or.2021.8083 Text en Copyright: © Tanaka et al. https://creativecommons.org/licenses/by/4.0/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
Tanaka, Tomohiro
Ohishi, Tomokazu
Asano, Teizo
Takei, Junko
Nanamiya, Ren
Hosono, Hideki
Sano, Masato
Harada, Hiroyuki
Kawada, Manabu
Kaneko, Mika K.
Kato, Yukinari
An anti-TROP2 monoclonal antibody TrMab-6 exerts antitumor activity in breast cancer mouse xenograft models
title An anti-TROP2 monoclonal antibody TrMab-6 exerts antitumor activity in breast cancer mouse xenograft models
title_full An anti-TROP2 monoclonal antibody TrMab-6 exerts antitumor activity in breast cancer mouse xenograft models
title_fullStr An anti-TROP2 monoclonal antibody TrMab-6 exerts antitumor activity in breast cancer mouse xenograft models
title_full_unstemmed An anti-TROP2 monoclonal antibody TrMab-6 exerts antitumor activity in breast cancer mouse xenograft models
title_short An anti-TROP2 monoclonal antibody TrMab-6 exerts antitumor activity in breast cancer mouse xenograft models
title_sort anti-trop2 monoclonal antibody trmab-6 exerts antitumor activity in breast cancer mouse xenograft models
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144932/
https://www.ncbi.nlm.nih.gov/pubmed/34013368
http://dx.doi.org/10.3892/or.2021.8083
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