Shen Shanshan, Chen Hong, Zhu Taofeng, Ma Xiuqin, Xu Jun, Zhu Wenjiao, Chen Ruhua, Xie Jing, Ma Tieliang, Jia Lei, Wang Yuan, Peng Chunyan
Department of Gastroenterology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing University, Nanjing, Jiangsu 210008, P.R. China.
The Affiliated Yixing Hospital of Jiangsu University, Yixing, Jiangsu 214200, P.R. China.
Oncol Lett. 2017 May;13(5):3169-3176. doi: 10.3892/ol.2017.5857. Epub 2017 Mar 14.
The reaction of divalent transition metal salts and (E)-N'-(1-(pyridin-2-yl)ethylidene)nicotinohydrazide (penh) led to the formation of [Mn(penh)] (complex 1), [Co(penh)] (complex 2), [Cu(penh)] (complex 3) and [Cd (penh)] (complex 4) complexes. The four complexes were characterized using elemental analyses, infrared spectra and single-crystal X-ray diffraction analyses. Subsequently, the complexes were used for cell level experiments to determine potential antitumor effects. The results demonstrated that the complexes exhibited a similar structure; however, they were crystallized with distinct space groups. In comparison with the uncomplexed penh ligand, all four complexes were able to markedly decrease the proliferation rate of various types of tumor cell, including the human lung cancer cell line A549, human gastric cancer cell line BGC823 and human esophageal cancer cell line Eca109, in a concentration-dependent manner. Furthermore, the complexes promoted tumor cell apoptosis, as demonstrated in the apoptosis assay, and this was confirmed using electrophoresis.
二价过渡金属盐与(E)-N'-(1-(吡啶-2-基)亚乙基)烟酰肼(penh)反应生成了[Mn(penh)](配合物1)、[Co(penh)](配合物2)、[Cu(penh)](配合物3)和[Cd(penh)](配合物4)配合物。通过元素分析、红外光谱和单晶X射线衍射分析对这四种配合物进行了表征。随后,将这些配合物用于细胞水平实验以确定潜在的抗肿瘤作用。结果表明,这些配合物具有相似的结构;然而,它们以不同的空间群结晶。与未配位的penh配体相比,所有四种配合物均能以浓度依赖的方式显著降低包括人肺癌细胞系A549、人胃癌细胞系BGC823和人食管癌细胞系Eca109在内的各种类型肿瘤细胞的增殖率。此外,如凋亡检测所示,这些配合物促进了肿瘤细胞凋亡,并且通过电泳得到了证实。