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S 9788逆转原代人肾癌细胞培养物中的固有多药耐药性

Reversal of inherent multidrug-resistance in primary human renal cell carcinoma cell cultures by S 9788.

作者信息

Efferth T, Dunn T A, Berlion M, Langenbahn H, Pommerenke E W, Volm M

机构信息

German Cancer Research Center, Heidelberg.

出版信息

Anticancer Res. 1993 Jul-Aug;13(4):905-8.

PMID:8102519
Abstract

In a panel of 14 primary cultures of human renal cell carcinomas the reversal of inherent multidrug-resistance by S 9788, a new triazinoaminopiperidine derivative, was analysed. In combination with doxorubicin S 9788 revealed an evident reversal of multidrug resistance in 12 cell cultures. Two cell cultures remained unaffected. An association between reversal and P-glycoprotein (P-170) expression suggests that S 9788 exerts its activity through P-glycoprotein.

摘要

在一组14种人肾细胞癌原代培养物中,分析了一种新型三嗪氨基哌啶衍生物S 9788对固有多药耐药性的逆转作用。与阿霉素联合使用时,S 9788在12种细胞培养物中显示出明显的多药耐药逆转作用。两种细胞培养物未受影响。逆转作用与P-糖蛋白(P-170)表达之间的关联表明,S 9788通过P-糖蛋白发挥其活性。

相似文献

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引用本文的文献

1
Investigation of multidrug resistance in cultured human renal cell carcinoma cells by 31P-NMR spectroscopy and treatment survival assays.利用31P核磁共振波谱和治疗存活分析研究培养的人肾癌细胞中的多药耐药性。
MAGMA. 2005 Jul;18(3):144-61. doi: 10.1007/s10334-005-0107-7. Epub 2005 Jun 23.
2
Phase IB study of doxorubicin in combination with the multidrug resistance reversing agent S9788 in advanced colorectal and renal cell cancer.阿霉素联合多药耐药逆转剂S9788治疗晚期结直肠癌和肾细胞癌的I B期研究
Br J Cancer. 1997;76(10):1376-81. doi: 10.1038/bjc.1997.563.
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In vitro activity of S 9788 on a multidrug-resistant leukemic cell line and on normal hematopoietic cells-reversal of multidrug resistance by sera from phase I-treated patients.
S 9788对多药耐药白血病细胞系和正常造血细胞的体外活性——I期治疗患者血清逆转多药耐药性
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