MicroRNA-708 prevents ethanol-induced hepatic lipid accumulation and inflammatory reaction via direct targeting ZEB1

PI3K/AKT/mTOR通路 癌症研究 小RNA 脂肪肝 炎症 酒精性肝病 蛋白激酶B 肝硬化 酒精性肝炎 肝细胞癌 化学 信号转导 细胞生物学 生物 医学 内科学 免疫学 生物化学 疾病 基因
作者
Shuang Hu,Yumin Liu,Chen Chen,Liang‐yun Li,Bo-yu Zhang,Jun Yang,Haodong Li,Xiao‐Ming Meng,Jun Li,Tao Xu,Huan Zhou
出处
期刊:Life Sciences [Elsevier]
卷期号:258: 118147-118147 被引量:12
标识
DOI:10.1016/j.lfs.2020.118147
摘要

Alcoholic liver disease (ALD) was a global liver disease which divided into liver inflammation, fatty liver, alcoholic hepatitis or cirrhosis. Abnormal expression levels of some microRNAs (miRNA) family members often lead to ALD and other liver diseases. MicroRNA-708 (miR-708) was known to suppress the proliferation and metastasis of hepatocellular carcinoma (HCC), but its role in the progression of ALD was not clear. In this study, the expression level of miR-708 was down-regulated in ethanol-induced L0-2 cells. ZEB1 could decrease the PPAR-α expression while increase the SREBP-1 expression. Meanwhile, the expression levels of TNF-α and IL-6 were up-regulated by ZEB1. Of note, ZEB1 aggravated the apoptotic rate of L0-2 cells induced by ethanol via inhibiting p-AKT and p-mTOR of AKT/mTOR signaling pathway. What's more, it was demonstrated that miR-708 family members particularly target ZEB1 3′-UTR regions and can down-regulate the expression level of ZEB1 in L0-2 cells. Sum up, these results indicated that miR-708 might inhibit the liver inflammation and lipid accumulation by targeting ZEB1 via regulating AKT/mTOR signaling pathway.
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