Khélifa T, Casabianca-Pignède M R, René B, Jacquemin-Sablon A
URA 147 CNRS, Unité de Biochimie-Enzymologie, Institut Gustave Roussy, Villejuif, France.
Mol Pharmacol. 1994 Aug;46(2):323-8.
Chinese hamster lung cells resistant to 9-OH-ellipticine, i.e., DC-3F/9-OH-E cells, are several hundredfold resistant to DNA topoisomerase II inhibitors. According to previous studies, this resistance is associated with reduced topoisomerase II activity (about 4-fold) and decreased capacity of the topoisomerase II inhibitors to induce stabilization of the cleavable complex (about 10-fold). In the present work, an antibody was raised against a fragment of human topoisomerase II alpha. This antibody, which recognizes both isoforms, was used to determine the amounts of topoisomerases II alpha and beta in the sensitive and resistant cells. Northern and immunoblot analyses showed that (i) in the parental DC-3F cells the alpha enzyme is about 20-fold more abundant than the beta enzyme and the enzyme isoforms undergo reciprocal regulation during the cell growth phases, with the expression of the alpha enzyme dropping at the plateau phase while the expression of the beta enzyme increases, and (ii) in the resistant cells the amount of alpha enzyme is about 4-5-fold smaller than that in the sensitive cells, whereas the beta enzyme is almost undetectable. Analysis of DNA restriction sites in several independently selected resistant subclones revealed some rearrangements in the beta gene in two clones. However, these gene alterations did not correlate with changes in the resistance level. The relative contribution of these different changes to the resistance phenotype is discussed.
对9-羟基玫瑰树碱具有抗性的中国仓鼠肺细胞,即DC-3F/9-OH-E细胞,对DNA拓扑异构酶II抑制剂有数百倍的抗性。根据先前的研究,这种抗性与拓扑异构酶II活性降低(约4倍)以及拓扑异构酶II抑制剂诱导可裂解复合物稳定的能力下降(约10倍)有关。在本研究中,制备了一种针对人拓扑异构酶IIα片段的抗体。这种能识别两种同工型的抗体,被用于测定敏感细胞和抗性细胞中拓扑异构酶IIα和β的含量。Northern印迹分析和免疫印迹分析表明:(i)在亲本DC-3F细胞中,α酶的丰度比β酶高约20倍,并且这两种酶同工型在细胞生长阶段经历相互调节,α酶的表达在平台期下降,而β酶的表达增加;(ii)在抗性细胞中,α酶的量比敏感细胞中的量小约4至5倍,而β酶几乎检测不到。对几个独立选择的抗性亚克隆中的DNA限制性位点进行分析,发现在两个克隆的β基因中有一些重排。然而,这些基因改变与抗性水平的变化并无关联。本文讨论了这些不同变化对抗性表型的相对贡献。