期刊文献+

发育及DNA损伤反应调节基因1mRNA在癫痫患者脑组织中的表达及临床意义

Increased expression and clinical significance of REDD1mRNA in the patients with epilepsy
暂未订购
导出
摘要 目的观察REDD1mRNA在癫痫患者脑组织中的表达及临床意义。方法将50例癫痫患者分成难治性(42例)和非难治性癫痫(8例)两组,用基因芯片和免疫荧光定量PCR分别检测脑组织中REDD1mRNA基因表达,并与对照组进行比较。结果基因芯片扫描提示REDD1mRNA在癫痫患者脑组织中与对照组比较表达明显增加,难治性癫痫组和非难治性癫痫组没有明显的表达差异,免疫荧光定量PCR的结果与基因芯片结果一致。结论 REDD1mRNA在癫痫患者脑部中存在高表达,这种高表达可能通过雷帕霉素哺乳动物靶标系统导致神经元坏死与凋亡。 Objective To investigate the expression and clinical signification of REDD1(regulated in development and DNA damage responses, REDD1) mRNA in the brain tissue of the epilepsy patients. Methods In tractable epilepsy(IE) and non-intractable epilepsy(NIE) were studied by using gene microarray screening and real-time fluorescence quantitative polymerase chain reaction (FQ-PCR) for REDD1 mRNA. Results In this study, the cDNA microarray analysis showed that REDD1 mRNA level in epilepsy patients was significantly higher than that of the control group. However ,there was no difference between IE patients and NIE patients. The results of FQ-PCR were coincided well with the cDNA microarray datas. Conclusion Our study suggests that upregulation of REDD1mRNA is seen in the patients with epilepsy. The gene expression of REDD1 in epilepsy is significantly higher thafi those of control brain samples. It might lead to the neural damage or apoptosis through the mammalian target of rapamycin.
出处 《中风与神经疾病杂志》 CAS CSCD 北大核心 2006年第2期167-169,共3页 Journal of Apoplexy and Nervous Diseases
关键词 REDD1 癫痫 基因芯片 免疫荧光定量PCR Regulated in development and DNA damage responses Epilepsy Gene microarray screening Real-time fluorescence quantitative PCR
  • 相关文献

参考文献14

  • 1Shoshani T,Faerman A,Mett I,et al.Identification of a novel hypoxia-inducible factor 1-responsive gene,RTP801,involved in apoptosis[J].Molec Cell Biol,2002,22:2283-2293.
  • 2Schena M,Shalon D,Davis RW,et al.Quantitative monitoring of gene expression patterns with a complementary DNA microarray[J].Science,1995,270:467-470.
  • 3Ellisen LW,Ramsayer KD,Johannessen CM,et al.REDD1,a developmentally regulated transcriptional target of p63 and p53,links p63 to regulation of reactive oxygen species[J].Molec Cell,2002,10:995-1005.
  • 4Amanda E,Greene MT,Todorova S,et al.Perspectives on the metabolic management of epilepsy through dietary reduction of glucose and elevation of ketone bodies[J].Journal of Neurochemistry,2003,86(3):529-537.
  • 5Vielhaber S,Oertzen JH,Kudin A,et al.Correlation of hippocampal glucose oxidation capacity and interictal FDG-PET in temporal lobe epilepsy[J].Epilepsia,2003,44(2):193-199.
  • 6Cornford EM,Shamsa K,Zeitzer JM,et al.Regional analyses of CNS microdialysate glucose and lactate in seizure patients[J].Epilepsia,2002,43 (11):1360-1371.
  • 7Reiling JH,Hafen E.The hypoxia-induced paralogs scylla and charybdis inhibit growth by down-regulating S6K activity upstream of TSC in drosophila[J].Genes Dev,2004,18:2879-2892.
  • 8Corradetti MN,Inoki K,Guan K,et al.The stress-inducted proteins RTP801 and RTP801L are negative regulators of the mammalian target of rapamycin pathway[J].J Biol Chem,2005,280(11):9769-9772.
  • 9Brugarolas J,Lei K,Hurley RL,et al.Regulation of mTOR function in response to hypoxia by REDD1 and the TSC1/TSC2 tumor suppressor complex[J].Genes Dev,2004,18 (23):2893-2904.
  • 10Fingar DC,Richardson C J,Tee AR,et al.mTOR controls cell cycle progression through its cell growth effectors S6K1 and 4E-BP1/eukaryotic translation initiation factor 4E[J].Mol Cell Biol,2004,24:200-216.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部