文章摘要

碳水化合物反应元件结合蛋白在肝癌中表达与作用

作者: 1耿西林, 1张煜, 1李晖, 1郑伟, 1张智勇, 1海军, 1杜立学
1 陕西省人民医院 肝胆外科,陕西 西安 710068
通讯: 杜立学 Email: lixuedu_xa@163.com
DOI: 10.3978/.10.3978/j.issn.1005-6947.2016.07.012

摘要

目的:探讨碳水化合物反应元件结合蛋白(ChREBP)在肝癌(HCC)中的表达与生物学作用。方法:分别用qRT-PCR、免疫组化、Western blot法检测73例HCC组织与癌旁组织以及多种HCC细胞系与正常肝细胞系中ChREBP的mRNA与蛋白表达;观察siRNA干扰ChREBP表达后,HCC细胞周期、凋亡以及增殖的变化。结果:ChREBP的mRNA与蛋白表达在HCC组织中表达均明显高于癌旁组织、在所有HCC细胞系中均明显高于正常肝细胞系(均P<0.05)。干扰ChREBP表达后,HCC细胞发生明显G1-S期阻滞、细胞增殖明显降低(均P<0.05),但细胞凋亡未发生明显变化(P>0.05)。结论:ChREBP在HCC中表达升高,且可能通过调控细胞周期促进HCC细胞的增殖,从而在HCC的发展中起了重要的作用。
关键词: 癌,肝细胞 抗原,肿瘤相关,碳水化合物 细胞周期 细胞增殖

Expression of carbohydrate response element binding protein in hepatocellular carcinoma and its functions

Authors: 1GENG Xilin, 1ZHANG Yu, 1LI Hui, 1ZHENG Wei, 1ZHANG Zhiyong, 1HAI Jun, 1DU Lixue
1 Department of Hepatobiliary Surgery, Shaanxi Provincial People's Hospital, Xi'an 710068, China

CorrespondingAuthor:DU Lixue Email: lixuedu_xa@163.com

Abstract

Objective: To investigate the expression of carbohydrate response element binding protein (ChREBP) and its biological actions in hepatocellular carcinoma (HCC). Methods: The mRNA and protein expressions of ChREBP in 73 specimens of HCC along with its adjacent tissue, as well as different HCC cell lines and normal hepatic cell line were determined by q-PCR, immunohistochemical staining and Western blot analysis, respectively. The changes in cell cycle, apoptosis and proliferation in HCC cells were observed after the siRNA interference of ChREBP2 expression. Results: Both mRNA and protein expressions of ChREBP were significantly increased in HCC tissue compared with tumor-adjacent tissue, and significantly increased in all studied HCC cell lines compared with normal hepatic cell line (all P<0.05). After interference of ChREBP2 expression, HCC cells presented significant G1/S phase arrest and inhibition of proliferation (both P<0.05), but apoptosis showed no significant change (P>0.05). Conclusion: ChREBP expression is elevated in HCC, which may probably promote proliferation of HCC cells through cell cycle regulation, and thereby plays an important role in the progression of HCC.
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