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培养的绒毛膜癌细胞对甲氨蝶呤敏感的机制。

Mechanism of methotrexate-sensitivity of choriocarcinoma cells in culture.

作者信息

Inoue T, Nagura E, Toyoda T, Ishizuka T, Gotoh S, Kawashima K, Tomoda Y, Nagai Y

机构信息

Department of Obstetrics and Gynecology, Nagoya University School of Medicine.

出版信息

Jpn J Cancer Res. 1988 Mar;79(3):400-5. doi: 10.1111/j.1349-7006.1988.tb01604.x.

Abstract

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 [3H]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.

摘要

比较了从绒毛膜癌建立的四种细胞系对甲氨蝶呤(MTX)的敏感性。在本文中,我们比较了甲氨蝶呤(MTX)的靶酶二氢叶酸还原酶(DHFR)的相对基因拷贝数,以阐明该基因的扩增是否与观察到的一种名为NaUCC-1的细胞系对MTX的相对抗性有关,该细胞系对MTX的抗性比其他细胞系高4至5倍,并且[3H]MTX的摄取减少。斑点印迹和Southern印迹杂交均未显示四种细胞系之间基因拷贝数有任何显著差异。因此,NaUCC-1细胞系对MTX的抗性是由于药物摄取减少,而不是靶基因的扩增。

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Methotrexate-induced resistance to dactinomycin in choriocarcinoma.甲氨蝶呤诱导的绒毛膜癌对放线菌素D的耐药性。
Cancer. 1988 Sep 1;62(5):873-7. doi: 10.1002/1097-0142(19880901)62:5<873::aid-cncr2820620504>3.0.co;2-k.

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