Targeting the overexpressed CREB inhibits esophageal squamous cell carcinoma cell growth

被引:18
|
作者
Chen, Ping [1 ]
Li, Miaomiao [1 ]
Hao, Qianyun [1 ]
Zhao, Xuesong [1 ]
Hu, Tao [1 ]
机构
[1] Zhengzhou Univ, Coll Basic Med Sci, Collaborat Innovat Ctr Henan Prov Canc Chemopreve, Zhengzhou 450001, Henan, Peoples R China
关键词
esophageal cancer; CREB; cell growth; cell migration; ELEMENT-BINDING PROTEIN; TRANSCRIPTION FACTORS; GENE-EXPRESSION; HUMAN-MELANOMA; CANCER; IDENTIFICATION; PROTOONCOGENE; METASTASIS; APOPTOSIS; SURVIVAL;
D O I
10.3892/or.2017.6167
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although several studies highlight the important role of cAMP-responsive element binding protein (CREB) in tumor progression, little is known concerning the expression and function of CREB in esophageal cancer. In the present study, the expression of CREB was evaluated using a human esophageal squamous cell carcinoma tissue array by immunohistochemical analysis, which was confirmed by western blot analysis of tissues from esophageal cancer, and adjacent esophageal tissue. The role of CREB on esophageal cancer cell growth was analyzed in vitro and in vivo. Results showed that CREB was overexpressed in esophageal squamous cell carcinomas tissues, which was positively correlated with lymph node metastasis and tumor-node-metastasis (TNM) stage of esophageal cancer patients. Downregulating the expression of CREB effectively reduced esophageal cell growth in vitro and in vivo, induced S phase cell cycle arrest, triggered apoptosis and inhibited cell migration and invasion. These findings suggested CREB as an attractive drug target for esophageal cancer.
引用
收藏
页码:1369 / 1377
页数:9
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