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Expression Behavior of 85‐kDa Membrane Protein in Adriamycin‐resistant Tumor Cells and the Inhibition of Human Tumor Growth in Athymic Mice by MRK‐20 Monoclonal Antibody against the Protein

Treatment of tumors with monoclonal antibodies against tumor antigen is one of the selective modalities for cancer therapy. We examined the therapeutic effect of MRK‐20 (IgG(1)), a murine monoclonal antibody against resistance‐associated 85‐kDa membrane protein. The 85‐kDa protein is expressed on th...

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Detalles Bibliográficos
Autores principales: Ishii, Shigetaka, Naito, Mikihiko, Tsuruo, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919210/
https://www.ncbi.nlm.nih.gov/pubmed/8370652
http://dx.doi.org/10.1111/j.1349-7006.1993.tb02043.x
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author Ishii, Shigetaka
Naito, Mikihiko
Tsuruo, Takashi
author_facet Ishii, Shigetaka
Naito, Mikihiko
Tsuruo, Takashi
author_sort Ishii, Shigetaka
collection PubMed
description Treatment of tumors with monoclonal antibodies against tumor antigen is one of the selective modalities for cancer therapy. We examined the therapeutic effect of MRK‐20 (IgG(1)), a murine monoclonal antibody against resistance‐associated 85‐kDa membrane protein. The 85‐kDa protein is expressed on the surface of multidrug‐resistant cells induced by adriamycin. This protein is also expressed in some multiple‐drug‐resistant cells, including atypical multidrug‐resistant cells. The protein, once lost during long‐term culture without adriamycin, was rapidly induced by treatment with adriamycin but not with vinblastine or etoposide, suggesting a close relationship of the protein with adriamycin resistance but not with multidrug resistance. The antibody MRK‐20 suppressed the growth of subcutaneously implanted tumors expressing the 85‐kDa protein. Adriamycin‐resistant human ovarian tumor 2780AD and innately resistant human erythroleukemia HEL cells in athymic mice were completely cured by treatment with MRK‐20 antibody when the antibody was administered i.v. 2 days after s.c. tumor implantation. On the other hand, MRK‐20 did not show any effect on the growth of the 85‐kDa protein‐negative A2780 human ovarian tumor. These results indicate that the effect of MRK‐20 is highly specific to cells expressing 85‐kDa protein.
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spelling pubmed-59192102018-05-11 Expression Behavior of 85‐kDa Membrane Protein in Adriamycin‐resistant Tumor Cells and the Inhibition of Human Tumor Growth in Athymic Mice by MRK‐20 Monoclonal Antibody against the Protein Ishii, Shigetaka Naito, Mikihiko Tsuruo, Takashi Jpn J Cancer Res Article Treatment of tumors with monoclonal antibodies against tumor antigen is one of the selective modalities for cancer therapy. We examined the therapeutic effect of MRK‐20 (IgG(1)), a murine monoclonal antibody against resistance‐associated 85‐kDa membrane protein. The 85‐kDa protein is expressed on the surface of multidrug‐resistant cells induced by adriamycin. This protein is also expressed in some multiple‐drug‐resistant cells, including atypical multidrug‐resistant cells. The protein, once lost during long‐term culture without adriamycin, was rapidly induced by treatment with adriamycin but not with vinblastine or etoposide, suggesting a close relationship of the protein with adriamycin resistance but not with multidrug resistance. The antibody MRK‐20 suppressed the growth of subcutaneously implanted tumors expressing the 85‐kDa protein. Adriamycin‐resistant human ovarian tumor 2780AD and innately resistant human erythroleukemia HEL cells in athymic mice were completely cured by treatment with MRK‐20 antibody when the antibody was administered i.v. 2 days after s.c. tumor implantation. On the other hand, MRK‐20 did not show any effect on the growth of the 85‐kDa protein‐negative A2780 human ovarian tumor. These results indicate that the effect of MRK‐20 is highly specific to cells expressing 85‐kDa protein. Blackwell Publishing Ltd 1993-07 /pmc/articles/PMC5919210/ /pubmed/8370652 http://dx.doi.org/10.1111/j.1349-7006.1993.tb02043.x Text en
spellingShingle Article
Ishii, Shigetaka
Naito, Mikihiko
Tsuruo, Takashi
Expression Behavior of 85‐kDa Membrane Protein in Adriamycin‐resistant Tumor Cells and the Inhibition of Human Tumor Growth in Athymic Mice by MRK‐20 Monoclonal Antibody against the Protein
title Expression Behavior of 85‐kDa Membrane Protein in Adriamycin‐resistant Tumor Cells and the Inhibition of Human Tumor Growth in Athymic Mice by MRK‐20 Monoclonal Antibody against the Protein
title_full Expression Behavior of 85‐kDa Membrane Protein in Adriamycin‐resistant Tumor Cells and the Inhibition of Human Tumor Growth in Athymic Mice by MRK‐20 Monoclonal Antibody against the Protein
title_fullStr Expression Behavior of 85‐kDa Membrane Protein in Adriamycin‐resistant Tumor Cells and the Inhibition of Human Tumor Growth in Athymic Mice by MRK‐20 Monoclonal Antibody against the Protein
title_full_unstemmed Expression Behavior of 85‐kDa Membrane Protein in Adriamycin‐resistant Tumor Cells and the Inhibition of Human Tumor Growth in Athymic Mice by MRK‐20 Monoclonal Antibody against the Protein
title_short Expression Behavior of 85‐kDa Membrane Protein in Adriamycin‐resistant Tumor Cells and the Inhibition of Human Tumor Growth in Athymic Mice by MRK‐20 Monoclonal Antibody against the Protein
title_sort expression behavior of 85‐kda membrane protein in adriamycin‐resistant tumor cells and the inhibition of human tumor growth in athymic mice by mrk‐20 monoclonal antibody against the protein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919210/
https://www.ncbi.nlm.nih.gov/pubmed/8370652
http://dx.doi.org/10.1111/j.1349-7006.1993.tb02043.x
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