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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1989
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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. |
format | Online Article Text |
id | pubmed-5917818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
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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