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Mechanism of Methotrexate‐sensitivity of Choriocarcinoma Cells in Culture

Four cell lines established from choriocarcinoma were compared for sensitivity to methotrexate (MTX). In this paper, we have compared the relative gene copy number of dihydrofolate reductase (DHFR), the target enzyme of methotrexate (MTX), in order to clarify whether or not amplification of the gene...

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Autores principales: Indue, Takami, Nagura, Eiichi, Toyoda, Tetsuya, Ishizuka, Takao, Gotoh, Setsuko, Kawashima, Kohei, Tomoda, Yutaka, Nagai, Yoshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917478/
https://www.ncbi.nlm.nih.gov/pubmed/2836349
http://dx.doi.org/10.1111/j.1349-7006.1988.tb01604.x
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author Indue, Takami
Nagura, Eiichi
Toyoda, Tetsuya
Ishizuka, Takao
Gotoh, Setsuko
Kawashima, Kohei
Tomoda, Yutaka
Nagai, Yoshiyuki
author_facet Indue, Takami
Nagura, Eiichi
Toyoda, Tetsuya
Ishizuka, Takao
Gotoh, Setsuko
Kawashima, Kohei
Tomoda, Yutaka
Nagai, Yoshiyuki
author_sort Indue, Takami
collection PubMed
description Four cell lines established from choriocarcinoma were compared for sensitivity to methotrexate (MTX). In this paper, we have compared the relative gene copy number of dihydrofolate reductase (DHFR), the target enzyme of methotrexate (MTX), in order to clarify whether or not amplification of the gene is involved in the relative resistance to MTX observed for one of the cell lines, designated NaUCC‐1, which is 4‐ to 5‐fold more resistant to MTX as compared with the other cell lines and exhibits a reduced uptake of [(3)H]MTX. Neither dot blot nor Southern blot hybridization revealed any significant difference in the gene copy number among the four cell lines. Therefore, the resistance to MTX of the NaUCC‐1 line is explained by a reduced uptake of the drug, rather than amplification of the target gene.
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spelling pubmed-59174782018-05-11 Mechanism of Methotrexate‐sensitivity of Choriocarcinoma Cells in Culture Indue, Takami Nagura, Eiichi Toyoda, Tetsuya Ishizuka, Takao Gotoh, Setsuko Kawashima, Kohei Tomoda, Yutaka Nagai, Yoshiyuki Jpn J Cancer Res Article Four cell lines established from choriocarcinoma were compared for sensitivity to methotrexate (MTX). In this paper, we have compared the relative gene copy number of dihydrofolate reductase (DHFR), the target enzyme of methotrexate (MTX), in order to clarify whether or not amplification of the gene is involved in the relative resistance to MTX observed for one of the cell lines, designated NaUCC‐1, which is 4‐ to 5‐fold more resistant to MTX as compared with the other cell lines and exhibits a reduced uptake of [(3)H]MTX. Neither dot blot nor Southern blot hybridization revealed any significant difference in the gene copy number among the four cell lines. Therefore, the resistance to MTX of the NaUCC‐1 line is explained by a reduced uptake of the drug, rather than amplification of the target gene. Blackwell Publishing Ltd 1988-03 /pmc/articles/PMC5917478/ /pubmed/2836349 http://dx.doi.org/10.1111/j.1349-7006.1988.tb01604.x Text en
spellingShingle Article
Indue, Takami
Nagura, Eiichi
Toyoda, Tetsuya
Ishizuka, Takao
Gotoh, Setsuko
Kawashima, Kohei
Tomoda, Yutaka
Nagai, Yoshiyuki
Mechanism of Methotrexate‐sensitivity of Choriocarcinoma Cells in Culture
title Mechanism of Methotrexate‐sensitivity of Choriocarcinoma Cells in Culture
title_full Mechanism of Methotrexate‐sensitivity of Choriocarcinoma Cells in Culture
title_fullStr Mechanism of Methotrexate‐sensitivity of Choriocarcinoma Cells in Culture
title_full_unstemmed Mechanism of Methotrexate‐sensitivity of Choriocarcinoma Cells in Culture
title_short Mechanism of Methotrexate‐sensitivity of Choriocarcinoma Cells in Culture
title_sort mechanism of methotrexate‐sensitivity of choriocarcinoma cells in culture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917478/
https://www.ncbi.nlm.nih.gov/pubmed/2836349
http://dx.doi.org/10.1111/j.1349-7006.1988.tb01604.x
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