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首页> 外文期刊>Nuclear Medicine Communications >Sodium butyrate enhances the expression of baculovirus-mediated sodium/iodide symporter gene in A549 lung adenocarcinoma cells.
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Sodium butyrate enhances the expression of baculovirus-mediated sodium/iodide symporter gene in A549 lung adenocarcinoma cells.

机译:丁酸钠可增强杆状病毒介导的钠/碘转运体基因在A549肺腺癌细胞中的表达。

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摘要

OBJECTIVE: Increased expression of sodium/iodide symporter (NIS) is required for reporter gene imaging and effective radioiodine treatment of tumor. We investigated whether increased accumulation of iodine can be induced by sodium butyrate through a newly developed baculoviral transfer of the human NIS (hNIS) gene in A549 human lung adenocarcinoma. METHODS: A recombinant baculovirus [Bac-cytomegalovirus (CMV)-hNIS] encoding hNIS gene under the control of the CMV promoter was constructed. After A549 cells were transfected with Bac-CMV-hNIS in the presence of sodium butyrate, the expression of hNIS protein was detected by immunofluorescence and western blot analysis. The uptake and efflux of iodine were determined after the incubation of the transfected cells with I-iodide in the presence or absence of sodium butyrate. RESULTS: Immunocytochemical staining and western blot analysis showed increased hNIS protein expression in A549 cells transfected with Bac-CMV-hNIS after sodium butyrate treatment. Bac-CMV-hNIS transfected A549 cells accumulated up to about nine times more I than nontransfected cells; the amount of I uptake increased in a sodium butyrate in dose-dependent manner (P<0.001). However, rapid efflux of radioactivity was observed, with 50% lost during the first 2 min after I-containing medium had been replaced by a nonradioactive medium. CONCLUSION: Our results indicated that an improved efficiency of baculovirus-mediated hNIS reporter gene imaging in lung adenocarcinoma is possible with treatment with sodium butyrate. However, additional conditions need to be defined to reduce the rapid efflux of radioiodine for the purpose of radionuclide therapy.
机译:目的:增加钠/碘同向转运体(NIS)的表达对于报告基因成像和有效的放射碘治疗肿瘤是必需的。我们调查了丁酸钠通过新开发的杆状病毒转移人NIS(hNIS)基因在A549人肺腺癌中是否能引起碘积累的增加。方法:构建了在CMV启动子控制下编码hNIS基因的重组杆状病毒[Bac-巨细胞病毒(CMV)-hNIS]。在丁酸钠存在下用Bac-CMV-hNIS转染A549细胞后,通过免疫荧光和Western blot分析检测hNIS蛋白的表达。在存在或不存在丁酸钠的情况下,将转染的细胞与碘化物一起孵育后,测定碘的摄取和流出。结果:免疫细胞化学染色和蛋白质印迹分析表明,丁酸钠处理后转染Bac-CMV-hNIS的A549细胞中hNIS蛋白表达增加。 Bac-CMV-hNIS转染的A549细胞积累的I比未转染的细胞高出约9倍。丁酸钠中的I摄取量呈剂量依赖性(P <0.001)。然而,观察到放射性的快速流出,在用非放射性介质代替含I的介质后的前2分钟内损失了50%。结论:我们的结果表明,丁酸钠可以治疗杆状病毒介导的hNIS报告基因在肺腺癌中的成像效率更高。但是,为了放射性核素治疗的目的,需要定义其他条件以减少放射性碘的快速流出。

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