徐金升, 白亚玲, 张俊霞, 崔立文, 张慧然, 张胜雷. EphrinA1-Fc对人肾透明细胞癌786-O细胞EphA2和ERK表达影响的研究[J]. 中国肿瘤临床, 2013, 40(16): 956-959. DOI: 10.3969/j.issn.1000-8179.20130415
引用本文: 徐金升, 白亚玲, 张俊霞, 崔立文, 张慧然, 张胜雷. EphrinA1-Fc对人肾透明细胞癌786-O细胞EphA2和ERK表达影响的研究[J]. 中国肿瘤临床, 2013, 40(16): 956-959. DOI: 10.3969/j.issn.1000-8179.20130415
Jinsheng XU, Yaling BAI, Junxia ZHANG, Liwen CUI, Huiran ZHANG, Shenglei ZHANG. Effect of EphrinA1-Fc on phosphorylation of EphA2 and ERK in 786-O renal carcinoma cells[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2013, 40(16): 956-959. DOI: 10.3969/j.issn.1000-8179.20130415
Citation: Jinsheng XU, Yaling BAI, Junxia ZHANG, Liwen CUI, Huiran ZHANG, Shenglei ZHANG. Effect of EphrinA1-Fc on phosphorylation of EphA2 and ERK in 786-O renal carcinoma cells[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2013, 40(16): 956-959. DOI: 10.3969/j.issn.1000-8179.20130415

EphrinA1-Fc对人肾透明细胞癌786-O细胞EphA2和ERK表达影响的研究

Effect of EphrinA1-Fc on phosphorylation of EphA2 and ERK in 786-O renal carcinoma cells

  • 摘要:
      目的  探讨EphrinA1-Fc对人肾透明细胞癌786-O细胞系促红细胞生成素产生肝细胞受体A2(EphA2)和细胞外调节蛋白激酶1/2(ERK1/2)磷酸化程度的影响。
      方法  应用可溶性配体EphrinA1-Fc干预人肾透明细胞癌786-O细胞系,采用Wsternblot方法分析不同时间点细胞内EphA2和ERK1/2的磷酸化程度。
      结果  EphrinA1-Fc干预5、10、30、60 min后,p-EphA2、p-ERK的相对表达量逐渐增加(F=9.392,P=0.025;F=4.428,P=0.041),p-EphA2、p- ERK在EphrinA1-Fc干预前均未见表达。
      结论  EphrinA1-Fc抑制肿瘤转移复发的可能机制之一是其促使肾透明细胞癌786-O细胞EphA2磷酸化而导致其降解实现。

     

    Abstract:
      Objective  To detect the effect of EphrinA1-Fc on the phosphorylation of EphA2 and extracellular signal-regulated kinase (ERK) in 786-O renal carcinoma cells (RCCs).
      Methods  The soluble ligand EphrinA1-Fc was used to inhibit the 786-O RCCs in vitro. Western blot analysis was used to examine the phosphorylation of EphA2 and ERK1/2 in the 786-O RCCs at different time points.
      Results  After the intervention with EphrinA1-Fc for 5, 10, 30, and 60 min, the expression of p-EphA2 increased (F=9.392, P= 0.025) as well as that of p-ERK (F=4.428, P=0.041). No p-EphA2 and p-ERK expression was observed in the pre-intervention group.
      Conclusion  One of the possible mechanisms of the inhibitory effect of EphrinA1-Fc on tumor metastasis and recurrence involves thephosphorylation of EphA2 by EphrinA1-Fc, leading to the degradation of EphA2.

     

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