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重楼苷 II 通过下调丝切蛋白活性和 AKT/NF-κB 通路抑制肝癌细胞增殖、迁移和侵袭。

Polyphyllin II inhibits liver cancer cell proliferation, migration and invasion through downregulated cofilin activity and the AKT/NF-κB pathway.

机构信息

Laboratory of Experimental Animal Disease Model, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.

Neuroscience & Metabolism Research, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University and Collaborative Innovation Center, Chengdu 610041, China.

出版信息

Biol Open. 2020 Feb 7;9(2):bio046854. doi: 10.1242/bio.046854.

Abstract

The morbidity and mortality of primary liver cancer is one of the highest amongst all cancers. Deficiency of effective treatment and characteristics of cancer metastasis are believed to be responsible for this situation, thus a great demand is required for new agent development. Polyphyllin II (PP2), an important steroidal saponin extracted from Rhizoma Paris, has emerged as a potential anti-cancer agent, but the effects of PP2 in liver cancers and its underlying mechanisms remain unexplored. In our study, we found that PP2 could remarkably suppress the proliferation of two liver cancer cell lines, HepG2 and BEL7402, resulting in significant cell death. Besides, low doses of PP2 have displayed properties that inhibit cellular motility and invasion of liver cancer cells. In addition, we have found that PP2-mediated cofilin activity suppression was implicated in the inhibition of liver cancer cell motility. Decreased expression of two major hydrolytic enzymes (MMP2/MMP9), through the AKT/NF-κB signaling pathway may also be also responsible for this process. Rescue experiments done with either non-phosphorylatable mutant cofilin-1 (S3A) transfection or an activator of the AKT pathway significantly reversed the inhibition effects of PP2 on liver cancer cells. Taken together, we report a potential agent for liver cancer treatment and reveal its underlying mechanisms.

摘要

原发性肝癌的发病率和死亡率是所有癌症中最高的之一。缺乏有效的治疗方法和癌症转移的特点被认为是造成这种情况的原因,因此需要开发新的药物。重楼皂苷 II(PP2)是从云南重楼中提取的一种重要甾体皂苷,已成为一种有潜力的抗癌药物,但 PP2 在肝癌中的作用及其潜在机制仍不清楚。在我们的研究中,我们发现 PP2 可显著抑制肝癌细胞系 HepG2 和 BEL7402 的增殖,导致显著的细胞死亡。此外,低剂量的 PP2 具有抑制肝癌细胞迁移和侵袭的特性。此外,我们发现 PP2 介导的丝切蛋白活性抑制与肝癌细胞迁移的抑制有关。通过 AKT/NF-κB 信号通路下调两种主要的水解酶(MMP2/MMP9)的表达也可能是导致这种现象的原因。用非磷酸化突变丝切蛋白-1(S3A)转染或 AKT 通路的激活剂进行的挽救实验显著逆转了 PP2 对肝癌细胞的抑制作用。综上所述,我们报告了一种治疗肝癌的潜在药物,并揭示了其潜在的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/7044461/457970677836/biolopen-9-046854-g1.jpg

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