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Synergistic Anti-tumour Effects of Quercetin and Oncolytic Adenovirus expressing TRAIL in Human Hepatocellular Carcinoma

机译:槲皮素和表达TRAIL的溶瘤腺病毒在人肝细胞癌中的协同抗肿瘤作用

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摘要

The combination of oncolytic adenoviruses and specific chemotherapy agents is fast emerging as a novel therapeutic approach for resistan the patocellular carcinoma (HCC) cells. A detailed analysis of the network between adenovirus and chemotherapeutic agents can help design an effective strategy to combat HCC. We sought to investigate whether a combined treatment of ZD55-TRAIL and quercetin can have an enhanced cell-killing effect on HCC cells. In-vitro experiments showed that quercetin can enhance ZD55-TRAIL mediated growth inhibition and apoptosis in HCC cells. In addition, we showed that quercetin reduced ZD55-TRAIL mediated NF-κB activation and down-regulated its downstream targets, which in turn promoted the pro-apoptotic action of ZD55-TRAIL. Furthermore, in-vivo experiments in mice injected with HuH-7 cells resulted in significantly greater reduction in tumour growth and volume following combined ZD55-TRAIL and quercetin treatment. In conclusion, we demonstrated that quercetin could sensitize human HCC cells to apoptosis via ZD55-TRAIL in-vitro and in-vivo and presented ZD55-TRAIL and quercetin combination as a suitable anti-HCC therapy.
机译:溶瘤腺病毒和特异性化学治疗剂的结合正在迅速兴起,作为一种抗癌细胞癌(HCC)细胞的新型治疗方法。对腺病毒和化疗药物之间网络的详细分析可以帮助设计有效的抗HCC策略。我们试图研究ZD55-TRAIL和槲皮素的联合治疗是否可以增强对HCC细胞的杀伤作用。体外实验表明槲皮素可以增强ZD55-TRAIL介导的HCC细胞生长抑制和凋亡。此外,我们显示槲皮素减少ZD55-TRAIL介导的NF-κB活化并下调其下游靶标,进而促进ZD55-TRAIL的促凋亡作用。此外,在注射了HuH-7细胞的小鼠中进行的体内实验导致ZD55-TRAIL和槲皮素联合治疗后肿瘤的生长和体积明显减少。总之,我们证明槲皮素可以通过ZD55-TRAIL体内和体外使人HCC细胞对细胞凋亡敏感,并提出ZD55-TRAIL和槲皮素的组合作为合适的抗HCC治疗药物。

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