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Construction of pETNF-P16 plasmid and its expression properties in EC9706 cell line induced by X-ray irradiation

机译:X射线照射诱导pETNF-P16质粒的构建及其在EC9706细胞中的表达特性

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AIM: Recombined plasmid pETNF-P16 was constructed to investigate its expression properties in esophageal squamous carcinoma cell line EC9706 induced by X-ray irradiation and the feasibility of gene-radiotherapy for esophageal carcinoma. METHODS: Recombined plasmid pETNF-P16 was constructed and transfected into EC9706 cells with lipofectamine. ELISA, Western blot, and immunocytochemistry were performed to determine the expression properties of pETNF-P16 in EC9706 after transfection induced by X-ray irradiation. RESULTS: Eukaryotic expression vector pETNF-P16 was successfully constructed and transfected into EC9706 cells. TNFα expressions were significantly increased in the transfected cells after different doses of X-ray irradiation than in those after 0Gy irradiation (1 192.330-2 026.518 pg/mL, P < 0.05-0.01), and the TNFα expressions and P16 were significantly higher 6-48 h after 2 Gy X-ray irradiation (358.963-585.571 pg/mL, P < 0.05-0.001). No P16 expression was detected in normal EC9706 cells. However, there was strong expression in the transfected and irradiation groups. CONCLUSION: X-ray irradiation induction could significantly enhance TNFα and P16 expression in EC9706 cells transfected with pETNF-P16 plasmid. These results may provide important experimental data and therapeutic potential for gene-radiotherapy of esophageal carcinoma.
机译:目的:构建重组质粒pETNF-P16,研究其在X线照射诱导的食管鳞癌EC9706细胞中的表达特性,以及基因放射治疗食管癌的可行性。方法:构建重组质粒pETNF-P16,并用lipofectamine转染EC9706细胞。进行了ELISA,Western blot和免疫细胞化学实验,以测定pETNF-P16在X射线辐照转染后在EC9706中的表达特性。结果:成功构建了真核表达载体pETNF-P16,并转染到EC9706细胞中。在不同剂量的X射线照射下,转染的细胞中TNFα表达明显高于0Gy照射后(1 192.330-2 026.518 pg / mL,P <0.05-0.01),并且TNFα表达和P16显着升高6在2 Gy X射线照射后-48小时(358.963-585.571 pg / mL,P <0.05-0.001)。在正常EC9706细胞中未检测到P16表达。然而,在转染和照射组中有强烈的表达。结论:X射线照射诱导pETNF-P16质粒转染的EC9706细胞可明显增强TNFα和P16的表达。这些结果可能为食管癌的基因放射治疗提供重要的实验数据和治疗潜力。

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