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Annonaceous acetogenins reverses drug resistance of human hepatocellular carcinoma BEL-7402/5-FU and HepG2/ADM cell lines

机译:丙酮酸非生成素逆转人肝细胞癌BEL-7402 / 5-FU和HepG2 / ADM细胞株的耐药性

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摘要

Hepatocellular carcinoma (HCC) is the most common tumor in worldwide and chemotherapy resistant is a severe obstacle in HCC treatment. Annonaceous acetogenins was a nature compound from Uvaria accuminata and it has show the anti-tumor proliferation activity in many types cancer. In this study, we showed that annonaceous acetogenins is correlated with the drug resistance reversal in human hepatocellular carcinoma BEL-7402/5-FU and HepG2/ADM cell lines. We found that cell apoptosis was improved and cell cycle was arrested, further, multidrug-resistance proteins such as MDR1, MRP1, Topo-IIα, GST-π, cyclin D1, Survivin and bcl-2 are down-regulated, however, intracellular Rh-123 and caspase-3/8 was up-regulated by Annonaceous acetogenins treatment. We also found that there was a decreased activity of NF-κB and Akt in Annonaceous acetogenins treatment groups. Therefore, we demonstrate that Akt/NF-κB pathway was involved in Annonaceous acetogenins reverses drug resistance of human hepatocellular carcinoma cells.
机译:肝细胞癌(HCC)是全球最常见的肿瘤,化疗耐药性是HCC治疗的严重障碍。丙酮酸非生成素是一种来自乌vari的天然化合物,在许多类型的癌症中均显示出抗肿瘤增殖活性。在这项研究中,我们显示了在人类肝细胞癌BEL-7402 / 5-FU和HepG2 / ADM细胞系中,非环己基产乙酸原与耐药逆转有关。我们发现细胞凋亡得到改善,细胞周期被阻止,此外,耐多药蛋白如MDR1,MRP1,Topo-IIα,GST-π,cyclin D1,Survivin和bcl-2被下调,但细胞内Rh -123和半胱氨酸天冬氨酸蛋白酶-3/8被Annaceaceous acetogenins处理上调。我们还发现,在Annanoaceous acetogenins治疗组中,NF-κB和Akt的活性降低。因此,我们证明Akt /NF-κB通路参与了无水产乙酸原素逆转人肝癌细胞的耐药性。

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