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Interaction of methotrexate an anticancer agent with copper(II) ions: coordination pattern DNA-cleaving properties and cytotoxic studies

机译:甲氨蝶呤(一种抗癌药)与铜离子的相互作用:配位模式DNA裂解特性和细胞毒性研究

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摘要

The acid–base properties and the Cu(II) binding processes of methotrexate (MTX) were characterized by selected spectroscopic techniques and potentiometric measurements. The pH titration data showed that MTX behaves as a triprotic ligand. The deprotonation constants were determined for α-COOH and γ-COOH groups and (N1)H+ from the pteridine ring. Taking all the obtained results into consideration, a coordination pattern was proposed. The DNA-cleaving activity and reactive oxygen species (ROS) generation were investigated for both MTX and the Cu(II)–MTX system. The complex displayed a promising nuclease activity toward plasmid DNA in the presence of hydrogen peroxide. Interestingly, the induction of ROS, such as hydroxyl radicals, superoxide anions or singlet oxygen, was excluded and a different mechanism of DNA degradation was proposed. As MTX is now commonly used in anticancer therapy i.e. against lung cancer, basic cell-based studies were carried out to establish if its Cu(II) complex exhibits higher cytotoxic properties than the ligand alone. Activities of both compounds were also tested against colon carcinoma. Moreover, the determined values of IC50 were confronted with the cytotoxic activity of cisplatin.Electronic supplementary materialThe online version of this article (doi:10.1007/s00044-014-1074-1) contains supplementary material, which is available to authorized users.
机译:通过选择的光谱技术和电位测量来表征甲氨蝶呤(MTX)的酸碱性质和Cu(II)结合过程。 pH滴定数据表明,MTX表现为三价配体。测定了α-COOH和γ-COOH基团的去质子常数,以及来自蝶啶环的(N1)H + 。考虑所有获得的结果,提出了一种协调模式。研究了MTX和Cu(II)–MTX系统的DNA裂解活性和活性氧(ROS)生成。在过氧化氢的存在下,该复合物显示出对质粒DNA有希望的核酸酶活性。有趣的是,排除了诸如羟基自由基,超氧阴离子或单线态氧等ROS的诱导,并提出了DNA降解的另一种机制。由于现在MTX通常用于抗癌治疗,即针对肺癌,因此进行了基于细胞的基础研究,以确定其Cu(II)复合物是否比单独的配体具有更高的细胞毒性。还测试了两种化合物的抗结肠癌活性。此外,IC50的测定值还具有顺铂的细胞毒性活性。电子补充材料本文的在线版本(doi:10.1007 / s00044-014-1074-1)包含补充材料,授权用户可以使用。

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