Cantoni O, Sestili P, Cattabeni F, Geroni C, Giuliani F
Istituto di Farmacologia e Farmacognosia, Universita' degli Studi di Urbino, Italy.
Cancer Chemother Pharmacol. 1990;27(1):47-51. doi: 10.1007/BF00689275.
The effects of 4'-epi-doxorubicin (4'E-Dx) and doxorubicin (Dx) on cell survival were investigated after treatments for 1 or 24 h. It was found that after short-term exposure, 4'E-Dx causes a higher level of killing than Dx, whereas a similar cytotoxic response is detectable after 24 h. Under the same experimental conditions (treatment for 1 or 24 h) at equimolar concentrations, the two anthracyclines were equally inhibitory to DNA or RNA synthesis. Both the degree and the rate of induction of DNA strand breakage over a 1-h drug exposure were higher for 4'E-Dx than for Dx. These data were related to results of experiments carried out to investigate the rates of uptake and egress of the anthracyclines. From this study we concluded that no relationship can be established between the cytotoxicity of 4'E-Dx and Dx and their ability to inhibit DNA and RNA synthesis. In addition, the different DNA-damaging action of the two drugs does not appear to be solely dependent on the different rates of cellular uptake.
研究了4'-表阿霉素(4'E-Dx)和阿霉素(Dx)在处理1小时或24小时后对细胞存活的影响。结果发现,短期暴露后,4'E-Dx比Dx具有更高的杀伤水平,而24小时后可检测到类似的细胞毒性反应。在等摩尔浓度的相同实验条件下(处理1小时或24小时),两种蒽环类药物对DNA或RNA合成的抑制作用相同。在1小时的药物暴露过程中,4'E-Dx诱导DNA链断裂的程度和速率均高于Dx。这些数据与研究蒽环类药物摄取和排出速率的实验结果相关。从这项研究中我们得出结论,4'E-Dx和Dx的细胞毒性与其抑制DNA和RNA合成的能力之间无法建立联系。此外,两种药物不同的DNA损伤作用似乎并不完全取决于细胞摄取速率的差异。