Towatari M, Adachi K, Marunouchi T, Saito H
First Department of Internal Medicine, Nagoya University School of Medicine, Japan.
Br J Haematol. 1998 Jun;101(3):548-51. doi: 10.1046/j.1365-2141.1998.00713.x.
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.
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。