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人白血病细胞系中诱导性反义RNA揭示DNA拓扑异构酶IIα在药物敏感性中起关键作用的证据

Evidence for a critical role of DNA topoisomerase IIalpha in drug sensitivity revealed by inducible antisense RNA in a human leukaemia cell line.

作者信息

Towatari M, Adachi K, Marunouchi T, Saito H

机构信息

First Department of Internal Medicine, Nagoya University School of Medicine, Japan.

出版信息

Br J Haematol. 1998 Jun;101(3):548-51. doi: 10.1046/j.1365-2141.1998.00713.x.

Abstract

To examine the role of human DNA topoisomerase IIalpha (topo IIalpha) in drug resistance, we selectively inhibited topo IIalpha gene expression in U937 human monocytic leukaemia cells stably transfected with a plasmid that allowed for Zn-mediated conditional expression of a human alpha-topo IIalpha antisense sequence. Expression of topo IIalpha mRNA was reduced to <30%, whereas no significant alteration of topo IIbeta mRNA expression was observed. Under these conditions, drug sensitivity to the topo-II-directed agents, etoposide and daunorubicin, was reduced to approximately 50%, whereas sensitivity to 4-hydroperoxy-cyclophosphamide (4-HC) was not altered. This suggests that a reduced amount of topo IIalpha mRNA may be sufficient for the resistance to topo II inhibitors in leukaemia cells.

摘要

为研究人类DNA拓扑异构酶IIα(拓扑异构酶IIα)在耐药性中的作用,我们在稳定转染了一个质粒的U937人单核细胞白血病细胞中选择性抑制拓扑异构酶IIα基因表达,该质粒允许锌介导的人α-拓扑异构酶IIα反义序列的条件性表达。拓扑异构酶IIα mRNA的表达降低至<30%,而未观察到拓扑异构酶IIβ mRNA表达的显著改变。在这些条件下,对拓扑异构酶II导向药物依托泊苷和柔红霉素的药物敏感性降低至约50%,而对4-氢过氧环磷酰胺(4-HC)的敏感性未改变。这表明,拓扑异构酶IIα mRNA量的减少可能足以使白血病细胞对拓扑异构酶II抑制剂产生耐药性。

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