Department of Chemistry, University of Isfahan, Isfahan 81746-73441, Islamic Republic of Iran.
J Photochem Photobiol B. 2013 Jul 5;124:27-33. doi: 10.1016/j.jphotobiol.2013.04.001. Epub 2013 Apr 11.
The ctDNA-binding properties and in vitro antitumor activity of three water soluble Keggin type polyoxometalates (POMs): K6H[CoW11O39CpZr]·nH2O, K6H[CoW11O39CpTi·nH2O and K7H2[CoW11O39CpFe]·nH2O (abbreviated as CoWCpZr, CoWCpTi and CoWCpFe, respectively) were investigated using UV-Vis absorption spectroscopy, fluorescence spectrophotometry, cyclic voltammetry and MTT assay. The results of UV-Vis, fluorescence and cyclic voltammetry rule out intercalating binding mode and propose the groove or outside stacking binding of these POMs with ctDNA. The values of 1.30×10(4) M(-1), 1.15×10(4) M(-1) and 3.10×10(3) M(-1) were obtained for binding constant of CoWCpZr, CoWCpTi and CoWCpFe to ctDNA, respectively. The redox potential of POMs shift to more negative values in the presence of ctDNA which can be related to domination of electrostatic interaction in this system. The antitumor activity tests of these polyoxometalates (POMs) were carried out on two types of human cancer cells, MCF-7 and HEK-293 by MTT method. The results show the higher antitumor activity of CoWCpFe respect to two other that is related to its highest penetrating effectiveness for MCF-7 cells. Therefore, the antitumor activity of these POMs depends not only on their affinity to ctDNA but also strongly on their penetration ability to the cell membrane.
三种水溶性 Keggin 型多金属氧酸盐(POM):K6H[CoW11O39CpZr]·nH2O、K6H[CoW11O39CpTi·nH2O 和 K7H2[CoW11O39CpFe]·nH2O(分别缩写为 CoWCpZr、CoWCpTi 和 CoWCpFe)的 ctDNA 结合性质和体外抗肿瘤活性采用紫外可见吸收光谱、荧光分光光度法、循环伏安法和 MTT 法进行了研究。紫外可见、荧光和循环伏安的结果排除了嵌入结合模式,并提出了这些 POM 与 ctDNA 的沟槽或外部堆积结合。CoWCpZr、CoWCpTi 和 CoWCpFe 与 ctDNA 的结合常数分别为 1.30×10(4)M(-1)、1.15×10(4)M(-1)和 3.10×10(3)M(-1)。在存在 ctDNA 的情况下,POM 的氧化还原电位向更负的方向移动,这可以与该体系中静电相互作用的主导地位有关。通过 MTT 法,在两种类型的人癌细胞 MCF-7 和 HEK-293 上对这些多金属氧酸盐(POM)的抗肿瘤活性进行了测试。结果表明,CoWCpFe 的抗肿瘤活性高于其他两种,这与其对 MCF-7 细胞的最高穿透效果有关。因此,这些 POM 的抗肿瘤活性不仅取决于它们与 ctDNA 的亲和力,还强烈取决于它们穿透细胞膜的能力。