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pEgr-TNFα基因联合放疗抑制食管癌细胞生长的实验研究 被引量:1

Experimental Study on Inhibition of pEgr-TNFα Gene Therapy Combined with Radiotherapy on Esophageal Cancer Cells
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摘要 背景与目的:研究pEgr-TNFα重组质粒在稳定转染的食管癌细胞中的辐射诱导表达,及其联合放射治疗抑制食管癌细胞生长的效果。材料与方法:将脂质体包裹的pEgr-TNFα重组质粒,转染食管癌细胞系EC9706中,经G418筛选,获得稳定表达的细胞;采用ELISA方法检测0.075Gy和2Gy剂量x射线诱导后TNFα的表达;观察该工种剂量X射线照射后,EC9706细胞的增长情况。结果:pEgr-TNFα重组质粒转染EC9706细胞,并获得稳定转染的细胞;大剂量x射线照射和低剂量X射线照射均可诱导TNFα表达增强,为对照组的6~6.3倍(P〈0.01);稳定转染的细胞经0.075Gy和2GyX射线照射,8d后细胞数明显低于未转染细胞组(P〈0.01)和稳定转染的假照射组(P〈0.01)。结论:体外pEgr-TNFα基因.放射联合治疗有明显的抑制食管癌细胞生长的作用。 BACKGROUND & AIM: To study the expression of pEgr-TNFα induced by ionizing irradiation in stably transfected esophageal cancer cells and to study the inhibition effects of pEgr-TNFα combined with ionizing irradiation on esophageal cancer cells. MATERIAL AND METHODS: Esophageal cancer cell line EC9706 was transfected with pEgr-TNFα plasmids and selected through G418 to get stable expression cells. TNFα expression was detected by ELISA. The inhibition effect of pEgr-TNFα was observed after different doses of X-ray irradiation, rESULTS: pEgr-TNFα plasmids were transfected into EC9706 cells with stable expression. High dose and low dose X-ray irradiation could all enhance the expression of TNFα, about 6-6.3 times of control group (P〈O.001) . Ceils stably transfected was given 0.075 Gy and 2 Gy X-ray irradiation, number of cells was less than non-transfected group and sham group (P 〈0.01- 0.001) 8 d later. CONCLUSION: pEgr-TNFα gene-radiotherapy can significantly inhibit the growth of esophageal cancer cells in vitro.
出处 《癌变.畸变.突变》 CAS CSCD 2006年第1期6-8,共3页 Carcinogenesis,Teratogenesis & Mutagenesis
基金 国家自然科学基金资助项目(No.30210103904) 广东省科技计划项目资助(No.2003C30304)
关键词 pEg-TNFα质粒 X射线照射 食管癌细胞 低剂量照射 pEgr-TNFα plasmid X-ray irradiation esophageal cancer cell low dose irradiation
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