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Evaluation of curcumin-mediated photodynamic therapy on the reverse of multidrug resistance in tumor cells

机译:姜黄素介导的光动力治疗对肿瘤细胞多药抗性相反的评价

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Curcumin (CUR) possesses photosensitive anti-tumor activity. However, photoactive CUR mainly targets tumor cells sensitive to chemotherapy, whereas the effect on multi-drug resistant cancer cells has not been fully investigated. The study aimed to investigate the anti-tumor activity of CUR on resistant MCF-7/ADM cells and its underlying mechanism providing insights into CUR-mediated PDT and a reference for reversing multidrug resistance. Cell apoptosis and morphological changes were detected by Annexin V-FITC/PI double staining and immunofluorescence, respectively. The apoptosis mechanism of CUR-mediated PDT was investigated by detecting the levels of reactive oxygen species (ROS), mitochondrial membrane potential, and related proteins. MTT and apoptosis results showed that CUR-mediated PDT significantly enhanced cytotoxicity and induced considerable cell apoptosis. After treatment with CUR-mediated PDT, cells became round in shape and shrunk, F-actin was loosely arranged, and the nucleus decreased in size. In addition, the level of ROS increased over time compared to the control and peaked at 6 h. CUR-mediated PDT induced alterations in the mitochondrial membrane potential, increased the release of mitochondrial cytochrome C (Cyt-c), and downregulated caspase-3/7/9, PARP, and P-gp. In conclusion, CUR-PDT induced apoptosis in resistant MCF-7/ADM cells primarily through endogenous mitochondrial apoptosis pathway. Besides apoptosis activation in resistant cells, the reverse of multidrug resistance was ascribed to the downregulation of P-gp expression to a degree.
机译:姜黄素(Cur)具有光敏抗肿瘤活性。然而,光活性CUR主要针对化疗敏感的肿瘤细胞,而对多毒性癌细胞的影响尚未得到充分调查。该研究旨在探讨耐药MCF-7 / ADM细胞的CUR的抗肿瘤活性及其潜在机制,提供了对Cur介导的PDT的见解以及反转多药耐药的参考。通过膜蛋白V-FITC / PI双染色和免疫荧光检测细胞凋亡和形态变化。通过检测反应性氧物质(ROS),线粒体膜电位和相关蛋白水平来研究Cur介导PDT的凋亡机制。 MTT和凋亡结果表明,Cur介导的PDT显着增强了细胞毒性并诱导了相当大的细胞凋亡。在用Cur介导的PDT处理后,细胞成形并缩小,松散地布置F-肌动蛋白,尺寸减小。此外,与对照相比,ROS的水平随着时间的推移而增加,并在6小时达到峰值。 Cur介导的PDT诱导的线粒体膜电位改变,增加了线粒体细胞色素C(CYT-C)的释放,以及下调的Caspase-3/7/9,PARP和P-GP。总之,Cur-PDT诱导抗性MCF-7 / ADM细胞的细胞凋亡主要通过内源性线粒体凋亡途径。除了在抗性细胞中的凋亡激活之外,多药耐药性的逆转均归因于P-GP表达的下调至一定程度。

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