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Attenuation of Cytotoxic Natural Product DNA Intercalating Agents by Caffeine

机译:咖啡因对细胞毒性天然产物DNA嵌入剂的抑制作用

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摘要

Many anti-tumor drugs function by intercalating into DNA. The xanthine alkaloid caffeine can also intercalate into DNA as well as form π-π molecular complexes with other planar alkaloids and anti-tumor drugs. The presence of caffeine could interfere with the intercalating anti-tumor drug by forming π-π molecular complexes with the drug, thereby blocking the planar aromatic drugs from intercalating into the DNA and ultimately lowering the toxicity of the drug to the cancer cells. The cytotoxic activities of several known DNA intercalators (berberine, camptothecin, chelerythrine, doxorubicin, ellipticine, and sanguinarine) on MCF-7 breast cancer cells, both with and without caffeine present (200 μg/mL) were determined. Significant attenuation of the cytotoxicities by caffeine was found. Computational molecular modeling studies involving the intercalating anti-tumor drugs with caffeine were also carried out using density functional theory (DFT) and the recently developed M06 functional. Relatively strong π–π interaction energies between caffeine and the intercalators were found, suggesting an “interceptor” role of caffeine protecting the DNA from intercalation.
机译:许多抗肿瘤药物通过插入DNA而起作用。黄嘌呤生物碱咖啡因也可以插入DNA中,并与其他平面生物碱和抗肿瘤药物形成π-π分子复合物。咖啡因的存在可通过与药物形成π-π分子复合物来干扰嵌入的抗肿瘤药物,从而阻止平面型芳香族药物嵌入DNA中,并最终降低药物对癌细胞的毒性。确定了几种已知的DNA嵌入剂(小ber碱,喜树碱,白屈菜红碱,阿霉素,玫瑰树碱和血红素碱)对MCF-7乳腺癌细胞(无论是否存在咖啡因)(200μg/ mL)的细胞毒活性。发现咖啡因显着减弱了细胞毒性。还使用密度泛函理论(DFT)和最近开发的M06泛函进行了涉及将嵌入的抗肿瘤药物与咖啡因的计算分子建模研究。在咖啡因和嵌入剂之间发现了相对较强的π-π相互作用能,这表明咖啡因保护DNA免受嵌入的“拦截器”作用。

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