INHIBITION OF PROTEIN-SYNTHESIS REDUCES THE CYTO-TOXICITY OF 4'-(9-ACRIDINYLAMINO)METHANESULFON-META-ANISIDIDE WITHOUT AFFECTING DNA BREAKAGE AND DNA TOPOISOMERASE II IN A MURINE MASTOCYTOMA CELL-LINE

被引：55

作者：

SCHNEIDER, E ^{[1
]}

LAWSON, PA ^{[1
]}

RALPH, RK ^{[1
]}

机构：

[1] UNIV AUCKLAND,DEPT CELLULAR & MOLEC BIOL,AUCKLAND,NEW ZEALAND

来源：

BIOCHEMICAL PHARMACOLOGY | 1989年 / 38卷 / 02期

关键词：

D O I：

10.1016/0006-2952(89)90036-1

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：263 / 269

页数：7

共 32 条

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[4] THE PRODUCTION OF TOPOISOMERASE-II-MEDIATED DNA CLEAVAGE IN HUMAN-LEUKEMIA CELLS PREDICTS THEIR SUSCEPTIBILITY TO 4'-(9-ACRIDINYLAMINO)METHANESULFON-M-ANISIDIDE (M-AMSA)
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[10] THE INTERACTION BETWEEN NUCLEAR TOPOISOMERASE-II ACTIVITY FROM HUMAN-LEUKEMIA CELLS, EXOGENOUS DNA, AND 4'-(9-ACRIDINYLAMINO) METHANESULFON-M-ANISIDIDE (M-AMSA) OR 4-(4,6-0-ETHYLIDENE-BETA-D-GLUCOPYRANOSIDE) (VP-16) INDICATES THE SENSITIVITY OF THE CELLS TO THE DRUGS
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[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 144 (02) : 787 - 793

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