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Epidermal growth factor receptor inhibitor AG1478 affects HepG2 cell proliferation, cell cycle, apoptosis and c-Myc protein expression in a dose-dependent manner

机译:表皮生长因子受体抑制剂AG1478以剂量依赖的方式影响HepG2细胞增殖,细胞周期,细胞凋亡和C-Myc蛋白表达

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The aim of this study was to observe the effect of AG1478, an inhibitor of the epidermal growth factor receptor, on cell proliferation, cell cycle and apoptosis of human hepatoma HepG2 cells. Cell counting kit-8 assay was employed to examine the survival rates of cultured HepG2 cells after treatments with different concentrations of AG1478 for 24?h. Flow cytometry was performed to determine the effect of AG1478 on cell cycle and apoptosis. Immunohistochemistry was used to measure the expression of c-Myc protein. The survival rates of human hepatoma HepG2 cells after treatments with 5, 10, 20 and 40 μmol/L of AG1478 for 24?h were 76.0%, 59.6%, 51.2% and 42.1%, respectively. The apoptotic rates after treatments with 5, 10, 20 and 40 μmol/L of AG1478 were (12.88?±?1.91)%, (23.16?±?2.67)%, (35.36?±?1.95)% and (47.16?±?3.78)%, respectively. HepG2 cells were mainly arrested in the G0/G1 phase after treatment with 10, 20 and 40 μmol/L of AG1478. The c-Myc protein was highly expressed in HepG2 cells, whereas treatment with 20 μmol/L AG1478 substantially inhibited its expression. Overall, AG1478 inhibited the proliferation of human hepatoma cells in vitro , arrested the cells in G0/G1 phase, induced apoptosis and reduced the expression of c-Myc protein. These results also indicated that AG1478 blocked the proliferation and induced apoptosis of hepatoma cells in a dose-dependent manner.
机译:本研究的目的是观察到表皮生长因子受体的抑制剂,对人肝癌HepG2细胞的细胞增殖,细胞周期和凋亡的影响。使用细胞计数试剂盒-8测定法检测在具有不同浓度的Ag1478的治疗后培养的HepG2细胞的存活率24μm。进行流式细胞术以确定AG1478对细胞周期和细胞凋亡的影响。免疫组织化学用于测量C-MYC蛋白的表达。将人肝癌HepG2细胞的存活率分别为5,10,20和40μmol/ L24Ω·H的治疗后的76.0%,59.6%,51.2%和42.1%。在5,10,20和40μmol/ L的治疗后的凋亡率为(12.88Ω±1.91)%,(23.16?±2.67)%,(35.36?±1.95)%和(47.16?± ?3.78)%分别。 HepG2细胞主要在用10,20和40μmol/ L的Ag1478处理后在G0 / G1相中被捕。 C-myc蛋白在HepG2细胞中高度表达,而20μmol/ L Ag1478的处理基本上抑制其表达。总体而言,AG1478抑制体外人肝癌细胞的增殖,在G0 / G1相中捕获细胞,诱导的细胞凋亡并降低了C-Myc蛋白的表达。这些结果还表明,AG1478以剂量依赖性方式阻断了肝癌细胞的增殖和诱导凋亡。

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