Wang Lu, Yu Kai, Zhou Bai-Bin, Su Zhan-Hua, Gao Song, Chu Li-Li, Liu Jia-Ren
Key Laboratory of Synthesis of Functional Materials and Green Catalysis Colleges of Heilongjiang Province, School of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, Heilongjiang 150025, the People's Republic of China.
Dalton Trans. 2014 Apr 28;43(16):6070-8. doi: 10.1039/c3dt53030b.
A new cobalt-based polyoxometalate, (Himi)2[Bi(2)W2(0)O(66)(OH)(4)Co2(H2O)(6)Na(4) (H2O)14] · 17H2O (imi = iminazole) (BWCN) has been synthesized and structurally characterized. The inhibitory activities against selected human cancer lines were also determined in this study. The cell viability and chemoresistance of BWCN on human colon carcinoma HT-29 cells were assessed by MTT (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazoliumbromide), cell morphology changes, a comet assay and western blot analysis. The typical morphologic changes of apoptosis and DNA damage indicated that BWCN could have a distinct proliferation inhibitory effect on cancer cells. BWCN as a chemotherapeutic agent also induced apoptosis on HT-29 cells and showed a significant expression of cleaved-caspase-3. These results suggested that the active site of BWCN is the polymeric anion based on the basic tectonic block {BiW(9)}, and the possible mechanism is related to the interference of DNA synthesis in cancer cells.
一种新型钴基多金属氧酸盐(Himi)2[Bi(2)W2(0)O(66)(OH)(4)Co2(H2O)(6)Na(4)(H2O)14]·17H2O(imi = 咪唑)(BWCN)已被合成并进行了结构表征。本研究还测定了其对选定人类癌细胞系的抑制活性。通过MTT(3-[4,5-二甲基噻唑-2-基]-2,5-二苯基溴化四氮唑)、细胞形态变化、彗星试验和蛋白质印迹分析评估了BWCN对人结肠癌HT-29细胞的细胞活力和化疗耐药性。凋亡和DNA损伤的典型形态学变化表明,BWCN对癌细胞可能具有明显的增殖抑制作用。BWCN作为一种化疗药物也诱导HT-29细胞凋亡,并显示出切割的半胱天冬酶-3的显著表达。这些结果表明,基于基本构造单元{BiW(9)},BWCN的活性位点是聚合阴离子,其可能的机制与干扰癌细胞中的DNA合成有关。