The expression and activation of ERK/MAPK pathway in human esophageal cancer cell line EC9706

• Published in: Molecular biology reports 2011-02, Vol.38 (2), p.865-872
• Main Authors: Zheng, Shu-Tao, Huo, Qi, Tuerxun, Aerziguli, Ma, Wen-Jing, Lv, Guo-Dong, Huang, Cong-Gai, Liu, Qing, Wang, Xing, Lin, Ren-Yong, Sheyhidin, Ilyar, Lu, Xiao-Mei
• Format: Article
• Language: English
• Subjects: Animal Anatomy; Animal Biochemistry; Base Sequence; Biomedical and Life Sciences; Butadienes - pharmacology; Dose-Response Relationship, Drug; Enzyme Activation; Enzyme Inhibitors - pharmacology; Esophageal Neoplasms - metabolism; Extracellular Signal-Regulated MAP Kinases - metabolism; Gene expression; Gene Expression Profiling; Gene Expression Regulation, Enzymologic; Gene Expression Regulation, Neoplastic; Head & neck cancer; Histology; Humans; Kinases; Life Sciences; MAP Kinase Signaling System; Molecular biology; Molecular Sequence Data; Morphology; Nitriles - pharmacology; Phosphorylation; Signal Transduction
• ISSN: 0301-4851; 1573-4978
• DOI: 10.1007/s11033-010-0178-z

While there have been more and more studies concerning mitogen-activated protein kinases (MAPKs) signaling pathways, which control many cellular complex programmes, such as cell proliferation, differentiation, cell death and embryogenesis. However, few studies are carried out about expression and activation of classical MAPKs, extracellular signal-regulated kinase1/2 (ERK1/2) in human esophageal cancer cell line. Therefore, in the present study, we investigated the expression and activation of ERK1/2 in human esophageal cancer cell line EC9706 and human normal esophageal epithelial cell line Heepic, which is as control. This study showed that ERK1/2 was transiently phosphorylated both in EC9706 and Heepic, the kinetics of which were slightly different. To further study the ERK/MAPK signaling pathway in EC9706 and Heepic cell line, U0126 a kind of specific inhibitor of MEK was used. This study showed that U0126 can block the phosphorylation of ERK1/2 in a short time, the complete inhibition concentration for EC9706 and Heepic cell line is 50 and 20 μM, respectively. Incidentally, to further investigate the different roles of ERK1 and ERK2, vector-based short hairpin interference vectors targeted on ERK1/2 was constructed. Moreover, the effective interference target sequence was screened out in a transient transfection manner. MTT experiment showed that ERK2 is more important than ERK1 in the proliferation of EC9706 cells.