Glypican-3对Huh-7肝癌细胞的抗癌作用

Ji-Yu Wen, Xiaojun Wen, Jinju Wang, Y. Shu, Z. Qiu, Zhong‐Kao Liu, Ran Li, Guo-fang Zeng, S. Bao, Huilai Miao, Yanfang Chen, Ming-yi Li
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引用次数: 1

摘要

目的:以往的研究表明,Glypican-3 (GPC3)可能是肝细胞癌的一个有价值的诊断标志物。本研究检测了GPC3过表达对Huh-7肝癌细胞的影响。方法:构建重组质粒载体pcDNA3.1 (+)-GPC3,在Huh-7细胞中进行GPC3过表达研究。RT-PCR和Western blotting检测GPC3基因表达。用5-乙基-2-脱氧尿苷(EdU)掺入法观察细胞增殖情况。流式细胞术分别采用碘化丙啶(PI)和Annexin V-FITC/PI染色检测细胞周期进程和凋亡情况。采用Boyden transsewell和Matrigel法检测细胞迁移和侵袭。结果:GPC3过表达能有效抑制Huh-7细胞增殖,诱导细胞周期阻滞于S期,增加细胞凋亡。此外,GPC3过表达显著抑制了Huh-7细胞的迁移和侵袭能力。结论:GPC3可能成为肝癌治疗的新靶点
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-cancer Effects of Glypican-3 on Huh-7 Hepatocellular Carcinoma Cells
Aim: Previous studies have suggested Glypican-3 (GPC3) could be a valuable diagnostic marker for hepatocellular carcinoma. This study examined the effects of overexpression of GPC3 on Huh-7 hepatoma cells. Methods: We constructed a recombinant plasmid vector pcDNA3.1 (+)-GPC3 for GPC3 overexpression studies in Huh-7 cells. RT-PCR and Western blotting were used to confirm GPC3 gene expression. Cell proliferation was evaluated by 5-ethynyl-2-deoxyuridine (EdU) incorporation assay. Cell cycle progression and apoptosis were determined by flow cytometry using propidium iodide (PI) and Annexin V-FITC/PI staining, respectively. Cell migration and invasion were examined by Boyden Transewll and Matrigel assays. Results: GPC3 overexpression effectively inhibited proliferation, induced cell cycle arrest at S phase and increased apoptosis in Huh-7 cells. Furthermore, GPC3 overexpression significantly inhibited the migration and invasion ability of Huh-7 cells. Conclusion: Our results demonstrate that GPC3 could be a new therapeutic target for hepatocellular carcinoma
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