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作 者:时婧[1] 高丰厚[1] 郭跃辉[1] 袁海花[1] 姜斌[1]
机构地区:[1]上海交通大学医学院附属第三人民医院肿瘤科,上海201900
出 处:《中华肿瘤防治杂志》2012年第6期419-422,共4页Chinese Journal of Cancer Prevention and Treatment
基 金:上海市科学技术委员会基金(10JC1409200);上海市宝山区科委基金(10-E-3)
摘 要:目的:探讨肺癌细胞中抑癌蛋白PTEN低表达的相关机制。方法:Western blot方法检测肺癌细胞和正常人肺上皮细胞BEAS-2BPTEN蛋白的表达;用放线菌酮(1μg/mL)处理人肺腺癌细胞A549和正常人肺上皮细胞BEAS-2B阻断细胞翻译后,Western blot方法检测不同时相PTEN蛋白的表达。RT-PCR检测肺癌细胞与正常肺上皮细胞PTEN mRNA水平;放线菌素D(1μg/mL)处理肺癌细胞与正常肺上皮细胞阻断新生RNA合成,RT-PCR检测不同时相PTEN mRNA的水平。结果:Western blot结果显示,肺癌细胞中PTEN蛋白表达与正常肺上皮细胞比较有不同程度的降低(0.38~1.32倍);使用放线菌酮处理A549和BEAS-2B后,24h内A549及BEAS-2B细胞PTEN蛋白表达无明显改变。RT-PCR结果显示肺癌细胞中PTEN mRNA与正常人肺上皮细胞相比明显降低(0.41~0.68倍);放线菌素D处理显示肺癌细胞PTEN mRNA降解速率比正常肺上皮细胞降解速率明显加快。结论:肺癌细胞中抑癌蛋白PTEN低表达的主要原因是其mRNA降解加速,这为进一步研究PTEN蛋白低表达的详细分子机制提供了线索。OBJECTIVE:To investigate the mechanisms of low expression of PTEN in lung cancer ceils. METHODS: Western blot was performed to detect the protein expression of PTEN in lung cancer cells and normal human lung epithelial cell. After translation inhibition with cycloheximide (1 μg/mL), PTEN protein levels were determined during different phases. The levels of PTEN mRNA were determined by RT-PCR in A549 and BEAS-2B. Then, the treatment of actinomycin D (1 μg/mL) for blocking transcription, evaluated PTEN mRNA at indicated time point in A549 and BEAS-2B cells. RESULTS: Western blot showed that the PTEN protein was obviously decreased by approximately 0. 38- 1.32 times in lung cancer cells than normal lung ceil. After using cycloheximide, PTEN protein expression in A549 had not changed significantly during 24 hours as well as BEAS-2B. RT-PCR results showed that PTEN mRNA levels were significantly dropped by 0.41-0.68 times in lung cancer cells, compared with BEAS-2B. The treatment with actinomycin D, PTEN mRNA degradation rate in lung cancer cells was much faster than that in BEAS-2B. CONCLUSION: These data indicates that PTEN mRNA degradation acceleration led to down-regulation of PTEN, which provids some clues for further investigating the PTEN expression molecular mechanisms in lung cancer cells.
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