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首页> 外文期刊>Cancer Cell International >A possible role for selenoprotein glutathione peroxidase (GPx1) and thioredoxin reductases (TrxR1) in thyroid cancer: our experience in thyroid surgery
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A possible role for selenoprotein glutathione peroxidase (GPx1) and thioredoxin reductases (TrxR1) in thyroid cancer: our experience in thyroid surgery

机译:硒蛋白谷胱甘肽过氧化物酶(GPx1)和硫氧还蛋白还原酶(TrxR1)在甲状腺癌中的可能作用:我们在甲状腺手术中的经验

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Oxidative stress is responsible for some alterations in the chemical structure and, consequently, in the function of proteins, lipids, and DNA. Recent studies have linked oxidative stress to cancers, particularly thyroid cancer, but the mechanisms remain unclear. Here, we further characterize the role of oxidative stress in thyroid cancer by analyzing the expression of two selenium antioxidant molecules, glutathione peroxidase (GPx1) and thioredoxin reductase (TrxR1) in thyroid cancer cells. Samples of both healthy thyroid tissue and thyroid tumor were taken for analysis after total thyroidectomy. The expression of GPx1 and TrxR1 was revealed by Western blot analysis and quantified by densitometric analyses, while the evaluation of free radicals was performed by Electron Paramagnetic Resonance (EPR)-spin trapping technique. Our results show a decrease in the expression of GPx1 and TrxR1 (??45.7 and ??43.2% respectively, p?
机译:氧化应激会导致化学结构发生某些变化,进而导致蛋白质,脂质和DNA的功能发生变化。最近的研究已经将氧化应激与癌症,尤其是甲状腺癌联系起来,但是其机制仍不清楚。在这里,我们通过分析两种硒抗氧化剂分子,谷胱甘肽过氧化物酶(GPx1)和硫氧还蛋白还原酶(TrxR1)在甲状腺癌细胞中的表达,进一步表征氧化应激在甲状腺癌中的作用。全甲状腺切除后,取出健康甲状腺组织和甲状腺肿瘤的样本进行分析。通过Western印迹分析揭示GPx1和TrxR1的表达,并通过光密度分析进行定量,而自由基的评估则通过电子顺磁共振(EPR)自旋捕获技术进行。我们的结果表明,与健康细胞相比,甲状腺癌细胞中GPx1和TrxR1的表达减少(分别为?? 45.7和?? 43.2%,p?<?0.01)。此外,EPR技术显示肿瘤组织中自由基的增加,明显高于健康甲状腺组织中的自由基的增加(+?116.3%,p?<?0.01)。我们的发现强调了甲状腺癌和氧化应激之间的关系,表明甲状腺癌组织中氧化剂/抗氧化剂系统的不平衡。这些结果表明,由于自由基的过度产生,无法产生足够的抗氧化剂防御能力或抗氧化剂的消耗增加,可能在甲状腺癌中起关键作用。

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