Shen Rui, Wang Weihua, Yang Gengliang
College of Pharmaceutical Sciences, Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Hebei University, Baoding, 071002, People's Republic of China,
J Fluoresc. 2014 May;24(3):959-66. doi: 10.1007/s10895-014-1380-5. Epub 2014 Apr 6.
In this work, a xanthone derivative was obtained by cationic modification of the free hydroxyl group of xanthone with dimethylamine group of high pKa value. The interactions of xanthones with DNA were investigated by spectroscopic methods, electrophoretic migration assay and polymerase chain reaction test. Results indicate that xanthones can intercalate into the DNA base pairs by the hydrophobic plane and the xanthone with dimethylamine side chain may also bind the DNA phosphate framework by the basic amine alkyl chain, thus showing a better DNA binding ability than the xanthone. Furthermore, inhibition on tumor cells (ECA109, SGC7901, GLC-82) proliferation of xanthones were evaluated by MTT method. Analysis results show that the xanthone with dimethylamine side chain exhibits more effective inhibition activity against three cancer cells than the xanthone. The effects on the inhibition of tumor cells in vitro agree with the studies of DNA binding. It means that the amine alkyl chain would play an important role in its antitumor activity and DNA binding property.
在本研究中,通过用高pKa值的二甲胺基团对呫吨酮的游离羟基进行阳离子修饰,得到了一种呫吨酮衍生物。采用光谱法、电泳迁移试验和聚合酶链反应试验研究了呫吨酮与DNA的相互作用。结果表明,呫吨酮可通过疏水平面插入DNA碱基对中,带有二甲胺侧链的呫吨酮还可通过碱性胺烷基链与DNA磷酸骨架结合,因此其DNA结合能力比呫吨酮更好。此外,采用MTT法评估了呫吨酮对肿瘤细胞(ECA109、SGC7901、GLC-82)增殖的抑制作用。分析结果表明,带有二甲胺侧链的呫吨酮对三种癌细胞的抑制活性比呫吨酮更有效。其对肿瘤细胞的体外抑制作用与DNA结合研究结果一致。这意味着胺烷基链在其抗肿瘤活性和DNA结合特性中发挥着重要作用。