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Antitumor activity of G-quadruplex-interactive agent TMPyP4 with photodynamic therapy in ovarian carcinoma cells

机译:G-四链体相互作用药物TMPyP4的光动力学治疗对卵巢癌细胞的抗肿瘤活性

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摘要

The aim of the present study was to investigate the potential effects of photodynamic therapy (PDT) mediated by the cationic porphyrin, 5,10,15,20-tetra-(N-methyl-4-pyridyl)porphine (TMPyP4), on an ovarian carcinoma cell line and the underlying mechanisms by which TMPyP4-PDT exerts its actions. The analysis of cell viability, hematoxylin and eosin staining and flow cytometric apoptosis assays revealed that TMPyP4-PDT potently suppressed the growth of the A2780 cells in a laser energy- and dose-dependent manner. Mechanically, it was observed that TMPyP4-PDT suppressed the proliferation and motility of the A2780 cells. In addition, the expression levels of minichromosome maintenance protein-2 (MCM2) and carbonic anhydrase IX (CA-IX) were detected by western blot analysis. The results indicated that the TMPyP4-PDT-induced apoptosis and antimetastatic activity in the A2780 cells was accompanied by the inhibition of the expression of MCM2 and CA-IX. Therefore, TMPyP4-PDT may represent a potential therapeutic method for the treatment of ovarian carcinoma.
机译:本研究的目的是研究阳离子卟啉5,10,15,20-四-(N-甲基-4-吡啶基)卟啉(TMPyP4)介导的光动力疗法(PDT)的潜在作用。卵巢癌细胞系及其TMPyP4-PDT发挥作用的潜在机制。细胞活力分析,苏木精和曙红染色以及流式细胞仪检测表明,TMPyP4-PDT以激光能量和剂量依赖性方式有效抑制A2780细胞的生长。在机械上,观察到TMPyP4-PDT抑制了A2780细胞的增殖和运动。另外,通过蛋白质印迹分析检测了微染色体维持蛋白2(MCM2)和碳酸酐酶IX(CA-IX)的表达水平。结果表明,TMPyP4-PDT诱导的A2780细胞凋亡和抗转移活性伴随MCM2和CA-IX表达的抑制。因此,TMPyP4-PDT可能代表了一种治疗卵巢癌的潜在治疗方法。

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