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机构地区:[1]徐州医学院研究生学院,江苏徐州221004 [2]徐州医学院附属医院介入放射科,江苏徐州221002
出 处:《徐州医学院学报》2013年第6期384-387,共4页Acta Academiae Medicinae Xuzhou
摘 要:目的建立辐射抗性食管癌细胞亚系TE-1R,并探讨其辐射诱导的凋亡性及辐射抗性机制。方法采用分次、间歇照射的方法(2Gy,5次)诱导人食管癌细胞系TE-1产生具有稳定辐射抗性的细胞亚系TE-1R,显微镜下观察细胞形态学差异。以TE-1和TE-1R细胞为实验对象,给予6MVX射线单次照射(2Gy),流式细胞仪分析细胞照射后的凋亡情况,RT—PCR法和Western Blot法分别检测食管癌TE-1、TE-1R细胞中复制蛋白AI(RPA1)mRNA和蛋白的表达情况。结果筛选出辐射抗性食管癌细胞亚系TE—1R。2Gy射线照射后12、24和48hTE-1R细胞的凋亡率低于TE—1细胞(P〈0.05)。RPA1 mRNA和蛋白在TE—1R细胞中的表达高于TE-1细胞(P〈0.05)。结论成功建立了辐射抗性的食管癌细胞亚系TE-1R,新的细胞亚系TE-1R比其亲本细胞系TE-1对射线更加抗拒,RPA1可能在食管癌细胞辐射抗性的修复中起着重要作用。Objective To establish radioresistant esophageal cancer cell subline TE - 1R and to study apoptosis induced by radiation and discuss its radioresistant mechanism. Methods To establish radioresistant esophageal cancer cell subline TE - 1 R by using graded, intermittent irradiation method (2 Gy 5 times), morphological changes were observed under the microscope. TE - 1 and TE - 1R were given 6 MV X ray single exposure 2 Gy. Effect of cell apoptosis after ir radiation was detected by flow cytometry. The expression level of RPA1 mRNA in human esophageal cancer cell TE - 1 and TE - 1R were determined by using reverse transcription -polymerase chain reaction (RT- PCR) and the expression of RPA1 protein was determined by Western blot. Results Esophageal cancer cell subline TE - IR was screened out. After 2 Gy irradiation, cell apoptosis rate of TE - 1R was lower than TE - 1. The expression of RPA1 mRNA and protein in the radioresistant esophageal cancer cell subline TE - 1R were higher than TE - 1. Conclusion We established ra- dioresistant esophageal cancer cell lines TE- 1R successfully. The new cell subline TE- 1R had stronger resistance than its parent cell lines TE - 1. The RPA1 may play an important role in radioresistance of esophageal cancer cell lines.
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