谷胱甘肽相关酶活性与肿瘤的关系:缺氧条件下 HepG2 细胞中谷胱甘肽过氧化物酶和谷胱甘肽还原酶的状态

O. Ozensoy Guler, Elif Ercan, T. Uysal
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引用次数: 0

摘要

在肝细胞癌(HCC)的肿瘤发生过程中,缺氧和活性氧(ROS)在改变肿瘤微环境(TME)方面起着至关重要的作用。迄今为止,缺氧诱导因子-1α(HIF-1α)、抗氧化酶谷胱甘肽过氧化物酶(GPx)和谷胱甘肽还原酶(GR)在缺氧条件下随时间变化的情况尚不清楚。因此,我们的主要目标是研究缺氧条件下谷胱甘肽过氧化物酶(GPx)和谷胱甘肽还原酶(GR)在 HCC 细胞株(HepG2)中的作用。 细胞裂解物中的 HIF-1α 蛋白水平通过酶联免疫吸附法测定,蛋白表达通过 Western 印迹法鉴定。细胞裂解液中的 GPx 和 GR 活性水平用分光光度法测定。 在正常缺氧和缺氧条件下,HIF-1α 蛋白水平均得到测定(p<0.001)。此外,在时间依赖性缺氧条件下也观察到了 HIF-1α 蛋白水平和表达,发现 HIF-1α 蛋白水平在 HepG2 细胞系中 4 小时达到峰值。我们还检测到,在缺氧 4 小时的情况下,GPx 活性水平降低,GR 活性水平升高(p<0.001)。 暴露于缺氧环境超过 4 小时会降低 HCC 细胞中 HIF-1α 的水平。根据这些结果,我们建议 HepG2 细胞株暴露于低氧环境的理想时间为 4 小时。此外,缺氧还能刺激 GPx 和 GR 的活性水平。我们的研究结果表明,GPx和/或GR酶的活性水平可能是缺氧依赖性HCC肿瘤发生过程中的治疗靶点。
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GSH-related enzyme activity and tumor relation: glutathione peroxidase and glutathione reductase status under hypoxia in HepG2 cells
In hepatocellular carcinoma (HCC), tumorigenesis, hypoxia and reactive oxygen species (ROS) play a crucial role in altering the tumor microenvironment (TME). Until now, the time-dependent alteration of hypoxia-inducible factor-1α (HIF-1α), the antioxidant enzymes glutathione peroxidase (GPx) and glutathione reductase (GR) under hypoxic conditions in HCC were not clear. Consequently, our main target was to investigate the role of GPx and GR status in HCC cell line (HepG2) under hypoxic conditions. HIF-1α protein levels in cell lysates were determined by ELISA assay and protein expressions were identified using western blot. GPx and GR activity levels of the cell lysates were measured spectrophotometrically. HIF-1α protein levels were determined under normoxic and hypoxic conditions (p<0.001). Also, HIF-1α protein levels and expressions were observed under time-dependent hypoxic conditions, the HIF-1α protein level is found to be reached its peak point at 4 h in the HepG2 cell line. We also have detected decreased activity levels of GPx and increased GR activity levels under hypoxia for 4 h (p<0.001). More than 4 h of exposure to hypoxic environment reducted the HIF-1α levels in HCC cells. According to the results, we suggest the ideal exposure time to hypoxic conditions as 4 h for the HepG2 cell line. In addition, hypoxia also stimulated the activity levels of GPx and GR. Our results suggest that the activity levels of GPx and/or GR enzymes may be therapeutic targets in the hypoxia-dependent HCC tumorigenesis process.
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