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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1988
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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. |
format | Online Article Text |
id | pubmed-5917478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1988 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
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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