摘要
目的探讨ESCCAL_1在食管鳞癌中发挥功能的可能机制。方法使用人磷酸化激酶阵列试剂盒检测ESCCAL_1敲减前后EC9706细胞中相关蛋白激酶磷酸化水平,对各蛋白条带进行灰度值定量分析。结果 KD组与NC组中FAK、JNK1、Src、AMPKα1等蛋白激酶的相对磷酸化水平比值分别为2.76∶1、2.20∶1、2.15∶1、2.01∶1,表达量明显降低(P<0.05)。结论 ESCCAL_1可能通过调节相关蛋白激酶的磷酸化水平调控EC9706细胞生长。
Objective To explore the possible mechanism of ESCCAL_I in esophageal squamous cell carcinoma. Methods Human phospho - kinase array kit was used to detect the phosphorylation of protein kinase in EC9706 cells transfected with ESC- CAL_I - shRNA or control. Each gray value of protein band was quantitatively analyzed. Results The relative gray value ratios of FAK,pJNK1 ,pSrc,pAMPKcd between KD group and NC group were 2.76:1, 2. 20:1, 2. 15:1, 2. 01:I respectively, and the phosphorylation of these protein kinases in KD group was significantly down - regulated (P 〈 0. 05). Conclusion ESCCAL_I may regulate the EC9706 cell proliferation and metastasis through protein kinase phosphorylation.
出处
《河南医学研究》
CAS
2016年第10期1731-1733,共3页
Henan Medical Research