MicroRNA-200a induces apoptosis by targeting ZEB2 in alcoholic liver disease

被引:30
|
作者
Zhao, Yu-xin [1 ,2 ,3 ]
Sun, Ying-yin [1 ,2 ,3 ]
Huang, Ai-ling [1 ,2 ,3 ]
Li, Xiao-feng [1 ,2 ,3 ]
Huang, Cheng [1 ,2 ,3 ]
Ma, Tao-tao [1 ,2 ,3 ]
Li, Jun [1 ,2 ,3 ]
机构
[1] Anhui Med Univ, Anhui Inst Innovat Drugs, Sch Pharm, Anhui Prov Key Lab Major Autoimmune Dis, Hefei 230000, Anhui, Peoples R China
[2] Minist Educ, Key Lab Antiinflammatory & Immune Med, Hefei 230000, Anhui, Peoples R China
[3] Anhui Med Univ, Inst Liver Dis, Hefei 230000, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Alcoholic liver disease; ALD; microRNA; miR-200a; ZEB2; Apoptosis; HEPATOCELLULAR-CARCINOMA; FEEDBACK LOOP; CANCER; INJURY; FAMILY; CELLS; METASTASIS; PROTEINS; INVASION; PATHWAY;
D O I
10.1080/15384101.2017.1417708
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
ABSTRATAlcoholic liver disease (ALD) and its complication continued to be a major health problem throughout the world. Increasing evidence suggests that microRNA (miRNA) that regulate apoptosis, inflammation and lipid metabolism are affected by alcohol in ALD. MiR-200a has emerged as a major regulator in several liver diseases, but its role in ALD has not been elucidated. The aim of this study is to figure out the biological function of miR-200a in ALD and to explore its underlying mechanism. The expression pattern of miR-200a were analyzed in vitro and in vivo, we showed that miR-200a was up-regulated in ALD in AML-12 and primary hepatocyte. We then examined it's effect on cell apoptosis and identified zinc finger E-box binding homeobox 2 (ZEB2; also known as SIP1) as a direct target gene of miR-200a. Furthermore, reintroduction of ZEB2 could reverse the pro-apoptosis of miR-200a on AML-12. Taken together, our study demonstrated that miR-200a regulates the apoptosis of hepatocyte in ALD by directly target ZEB2, both of which could serve as new therapeutic targets for ALD.
引用
收藏
页码:250 / 262
页数:13
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