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Inhibition of Multidrug‐resistant Human Tumor Growth in Athymic Mice by Anti‐P‐glycoprotein Monoclonal Antibodies

In an effort to devise an effective treatment for human drug‐resistant cancers, we have developed monoclonal antibodies, MRK16 and 17, reactive to the multidrug transporter protein, P‐glycoprotein. The monoclonal antibodies given intravenously effectively prevented tumor development in athymic mice...

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Detalles Bibliográficos
Autores principales: Tsuruo, Takashi, Hamada, Hirofumi, Sato, Shigeo, Heike, Yuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917818/
https://www.ncbi.nlm.nih.gov/pubmed/2571602
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01688.x
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author Tsuruo, Takashi
Hamada, Hirofumi
Sato, Shigeo
Heike, Yuji
author_facet Tsuruo, Takashi
Hamada, Hirofumi
Sato, Shigeo
Heike, Yuji
author_sort Tsuruo, Takashi
collection PubMed
description In an effort to devise an effective treatment for human drug‐resistant cancers, we have developed monoclonal antibodies, MRK16 and 17, reactive to the multidrug transporter protein, P‐glycoprotein. The monoclonal antibodies given intravenously effectively prevented tumor development in athymic mice inoculated subcutaneously with drug‐resistant human ovarian cancer cells 2780(AD). Treatment with MRK16 induced rapid regression of established subcutaneous tumors and apparent cures of some animals. Complement‐dependent cytotoxicity (MRK16) and antibody‐dependent cell‐mediated cytolysis (MRK16 and 17) were observed with these antibodies. These monoclonal antibodies may have potential as treatment tools against multidrug resistant human tumors possessing the P‐glycoprotein.
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spelling pubmed-59178182018-05-11 Inhibition of Multidrug‐resistant Human Tumor Growth in Athymic Mice by Anti‐P‐glycoprotein Monoclonal Antibodies Tsuruo, Takashi Hamada, Hirofumi Sato, Shigeo Heike, Yuji Jpn J Cancer Res Article In an effort to devise an effective treatment for human drug‐resistant cancers, we have developed monoclonal antibodies, MRK16 and 17, reactive to the multidrug transporter protein, P‐glycoprotein. The monoclonal antibodies given intravenously effectively prevented tumor development in athymic mice inoculated subcutaneously with drug‐resistant human ovarian cancer cells 2780(AD). Treatment with MRK16 induced rapid regression of established subcutaneous tumors and apparent cures of some animals. Complement‐dependent cytotoxicity (MRK16) and antibody‐dependent cell‐mediated cytolysis (MRK16 and 17) were observed with these antibodies. These monoclonal antibodies may have potential as treatment tools against multidrug resistant human tumors possessing the P‐glycoprotein. Blackwell Publishing Ltd 1989-07 /pmc/articles/PMC5917818/ /pubmed/2571602 http://dx.doi.org/10.1111/j.1349-7006.1989.tb01688.x Text en
spellingShingle Article
Tsuruo, Takashi
Hamada, Hirofumi
Sato, Shigeo
Heike, Yuji
Inhibition of Multidrug‐resistant Human Tumor Growth in Athymic Mice by Anti‐P‐glycoprotein Monoclonal Antibodies
title Inhibition of Multidrug‐resistant Human Tumor Growth in Athymic Mice by Anti‐P‐glycoprotein Monoclonal Antibodies
title_full Inhibition of Multidrug‐resistant Human Tumor Growth in Athymic Mice by Anti‐P‐glycoprotein Monoclonal Antibodies
title_fullStr Inhibition of Multidrug‐resistant Human Tumor Growth in Athymic Mice by Anti‐P‐glycoprotein Monoclonal Antibodies
title_full_unstemmed Inhibition of Multidrug‐resistant Human Tumor Growth in Athymic Mice by Anti‐P‐glycoprotein Monoclonal Antibodies
title_short Inhibition of Multidrug‐resistant Human Tumor Growth in Athymic Mice by Anti‐P‐glycoprotein Monoclonal Antibodies
title_sort inhibition of multidrug‐resistant human tumor growth in athymic mice by anti‐p‐glycoprotein monoclonal antibodies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917818/
https://www.ncbi.nlm.nih.gov/pubmed/2571602
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01688.x
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