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Multidrug Resistance in Cultured Human Leukemia and Lymphoma Cell Lines Detected by a Monoclonal Antibody, MRK16

Forty cultured human leukemia and lymphoma cell lines never exposed to anticancer agents in culture, apart from doxorubicin (ADM)‐resistant K562/ADM, were examined for reactivity with a monoclonal antibody, MRK16 in F(ab′)(2) form [MRK16‐F(ab′)(2)], which recognizes P‐glycoprotein (P‐gp). The relati...

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Autores principales: Ishida, Yasushi, Ohtsu, Tomoko, Hamada, Hirofumi, Sugimoto, Yoshikazu, Tobinai, Kensei, Minato, Keisuke, Tsuruo, Takashi, Shimoyama, Masanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917883/
https://www.ncbi.nlm.nih.gov/pubmed/2575608
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01641.x
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author Ishida, Yasushi
Ohtsu, Tomoko
Hamada, Hirofumi
Sugimoto, Yoshikazu
Tobinai, Kensei
Minato, Keisuke
Tsuruo, Takashi
Shimoyama, Masanori
author_facet Ishida, Yasushi
Ohtsu, Tomoko
Hamada, Hirofumi
Sugimoto, Yoshikazu
Tobinai, Kensei
Minato, Keisuke
Tsuruo, Takashi
Shimoyama, Masanori
author_sort Ishida, Yasushi
collection PubMed
description Forty cultured human leukemia and lymphoma cell lines never exposed to anticancer agents in culture, apart from doxorubicin (ADM)‐resistant K562/ADM, were examined for reactivity with a monoclonal antibody, MRK16 in F(ab′)(2) form [MRK16‐F(ab′)(2)], which recognizes P‐glycoprotein (P‐gp). The relative resistance index to various drugs was calculated by dividing the 50% growth inhibitory concentration (IC(50)) of the test cell line by IC(50) of K562, which was the negative control in the antibody experiment. MRK16‐F(ab′)(2) reacted with four cell lines, K562/ADM, KYO‐1, HEL and CMK, which had relative resistance index values of 2 or more to vincristine (VCR), vindesine, vinblastine, ADM, daunorubicin, mitoxantrone (MIT), etoposide (VP‐16) and actinomycin‐D (ACT‐D). The level of resistance to VCR and ADM in these cell lines decreased significantly in the presence of 10 μM verapamil in vitro. Significant expression of mRNA of P‐gp gene was also detected in K562/ADM, KYO‐1 and HEL. MRK16‐F(ab′)(2) did not react with 36 other cell lines. Among them, three cell lines, PL‐21, P31/FUJ and KOPM‐28, had relative resistance index values of 2 or more to anthracyclines, MIT and VP‐16, but not to vinca alkaloids or ACT‐D. The level of ADM‐resistance in these cell lines did not decrease significantly in the presence of 10 μM verapamil. Five cell lines, ATL‐1K, HL‐60, KMOE‐2, ML‐1 and U266, had relative resistance index values of 2 or more to some of the drugs, but not to the others, and 19 other cell lines did not. These results indicate that the reactivity of MRK16‐F(ab′)(2) correlates with a relative resistance index of 2 or more to all these drugs in cultured human leukemia and lymphoma cell lines.
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spelling pubmed-59178832018-05-11 Multidrug Resistance in Cultured Human Leukemia and Lymphoma Cell Lines Detected by a Monoclonal Antibody, MRK16 Ishida, Yasushi Ohtsu, Tomoko Hamada, Hirofumi Sugimoto, Yoshikazu Tobinai, Kensei Minato, Keisuke Tsuruo, Takashi Shimoyama, Masanori Jpn J Cancer Res Article Forty cultured human leukemia and lymphoma cell lines never exposed to anticancer agents in culture, apart from doxorubicin (ADM)‐resistant K562/ADM, were examined for reactivity with a monoclonal antibody, MRK16 in F(ab′)(2) form [MRK16‐F(ab′)(2)], which recognizes P‐glycoprotein (P‐gp). The relative resistance index to various drugs was calculated by dividing the 50% growth inhibitory concentration (IC(50)) of the test cell line by IC(50) of K562, which was the negative control in the antibody experiment. MRK16‐F(ab′)(2) reacted with four cell lines, K562/ADM, KYO‐1, HEL and CMK, which had relative resistance index values of 2 or more to vincristine (VCR), vindesine, vinblastine, ADM, daunorubicin, mitoxantrone (MIT), etoposide (VP‐16) and actinomycin‐D (ACT‐D). The level of resistance to VCR and ADM in these cell lines decreased significantly in the presence of 10 μM verapamil in vitro. Significant expression of mRNA of P‐gp gene was also detected in K562/ADM, KYO‐1 and HEL. MRK16‐F(ab′)(2) did not react with 36 other cell lines. Among them, three cell lines, PL‐21, P31/FUJ and KOPM‐28, had relative resistance index values of 2 or more to anthracyclines, MIT and VP‐16, but not to vinca alkaloids or ACT‐D. The level of ADM‐resistance in these cell lines did not decrease significantly in the presence of 10 μM verapamil. Five cell lines, ATL‐1K, HL‐60, KMOE‐2, ML‐1 and U266, had relative resistance index values of 2 or more to some of the drugs, but not to the others, and 19 other cell lines did not. These results indicate that the reactivity of MRK16‐F(ab′)(2) correlates with a relative resistance index of 2 or more to all these drugs in cultured human leukemia and lymphoma cell lines. Blackwell Publishing Ltd 1989-10 /pmc/articles/PMC5917883/ /pubmed/2575608 http://dx.doi.org/10.1111/j.1349-7006.1989.tb01641.x Text en
spellingShingle Article
Ishida, Yasushi
Ohtsu, Tomoko
Hamada, Hirofumi
Sugimoto, Yoshikazu
Tobinai, Kensei
Minato, Keisuke
Tsuruo, Takashi
Shimoyama, Masanori
Multidrug Resistance in Cultured Human Leukemia and Lymphoma Cell Lines Detected by a Monoclonal Antibody, MRK16
title Multidrug Resistance in Cultured Human Leukemia and Lymphoma Cell Lines Detected by a Monoclonal Antibody, MRK16
title_full Multidrug Resistance in Cultured Human Leukemia and Lymphoma Cell Lines Detected by a Monoclonal Antibody, MRK16
title_fullStr Multidrug Resistance in Cultured Human Leukemia and Lymphoma Cell Lines Detected by a Monoclonal Antibody, MRK16
title_full_unstemmed Multidrug Resistance in Cultured Human Leukemia and Lymphoma Cell Lines Detected by a Monoclonal Antibody, MRK16
title_short Multidrug Resistance in Cultured Human Leukemia and Lymphoma Cell Lines Detected by a Monoclonal Antibody, MRK16
title_sort multidrug resistance in cultured human leukemia and lymphoma cell lines detected by a monoclonal antibody, mrk16
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917883/
https://www.ncbi.nlm.nih.gov/pubmed/2575608
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01641.x
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