TY - JOUR
T1 - Interplays of liver fibrosis-associated microRNAs: Molecular mechanisms and implications in diagnosis and therapy
AU - Li, Hong
AU - Liu, Tingli
AU - Yang, Yongchun
AU - Cho, William C.
AU - Flynn, Robin J.
AU - Harandi, Majid Fasihi
AU - Song, Houhui
AU - Luo, Xuenong
AU - Zheng, Yadong
N1 - Publisher Copyright:
© 2022 Chongqing Medical University
PY - 2022/9/1
Y1 - 2022/9/1
N2 - microRNAs (miRNAs) are a class of non-coding functional small RNA composed of 21–23 nucleotides, having multiple associations with liver fibrosis. Fibrosis-associated miRNAs are roughly classified into pro-fibrosis or anti-fibrosis types. The former is capable of activating hepatic stellate cells (HSCs) by modulating pro-fibrotic signaling pathways, mainly including TGF-β/SMAD, WNT/β-catenin, and Hedgehog; the latter is responsible for maintenance of the quiescent phenotype of normal HSCs, phenotypic reversion of activated HSCs (aHSCs), inhibition of HSCs proliferation and suppression of the extracellular matrix-associated gene expression. Moreover, several miRNAs are involved in regulation of liver fibrosis via alternative mechanisms, such as interacting between hepatocytes and other liver cells via exosomes and increasing autophagy of aHSCs. Thus, understanding the role of these miRNAs may provide new avenues for the development of novel interventions against hepatic fibrosis.
AB - microRNAs (miRNAs) are a class of non-coding functional small RNA composed of 21–23 nucleotides, having multiple associations with liver fibrosis. Fibrosis-associated miRNAs are roughly classified into pro-fibrosis or anti-fibrosis types. The former is capable of activating hepatic stellate cells (HSCs) by modulating pro-fibrotic signaling pathways, mainly including TGF-β/SMAD, WNT/β-catenin, and Hedgehog; the latter is responsible for maintenance of the quiescent phenotype of normal HSCs, phenotypic reversion of activated HSCs (aHSCs), inhibition of HSCs proliferation and suppression of the extracellular matrix-associated gene expression. Moreover, several miRNAs are involved in regulation of liver fibrosis via alternative mechanisms, such as interacting between hepatocytes and other liver cells via exosomes and increasing autophagy of aHSCs. Thus, understanding the role of these miRNAs may provide new avenues for the development of novel interventions against hepatic fibrosis.
KW - Diagnosis
KW - Hepatic stellate cell
KW - Liver fibrosis
KW - Therapy
KW - miRNA
UR - https://doi.org/10.1016/j.gendis.2022.08.013
UR - http://www.scopus.com/inward/record.url?scp=85138834463&partnerID=8YFLogxK
U2 - 10.1016/j.gendis.2022.08.013
DO - 10.1016/j.gendis.2022.08.013
M3 - Review article
JO - Genes & Diseases
JF - Genes & Diseases
ER -