PMID- 34790726 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220428 IS - 2305-5839 (Print) IS - 2305-5847 (Electronic) IS - 2305-5839 (Linking) VI - 9 IP - 20 DP - 2021 Oct TI - MiR-34a promotes fibrosis of hepatic stellate cells via the TGF-beta pathway. PG - 1520 LID - 10.21037/atm-21-5005 [doi] LID - 1520 AB - BACKGROUND: Previous studies have confirmed that MicroRNA (miRNA) is a key regulator exhibiting different effects in human liver fibrosis. However, the function of miR-34a in liver fibrosis has not been reported. Hence, this study aimed to investigate the regulatory mechanism of miR-34a in liver fibrosis. METHODS: The expression of miR-34a was measured in fibrosis tissues via the quantitative real-time PCR (qRT-PCR) assay. Subsequently, 30 male C57BL/6J mice were divided into control and treatment groups and used to establish animal models of liver fibrosis to explore the expression level of miR-34a. Moreover, Cell Counting Kit 8 (CCK-8) and transwell assays were preformed to identify the regulatory mechanism of miR-34a in cells. The effect of miR-34a on the activity of transforming growth factor-beta (TGF-beta) pathway was observed by western blot. RESULTS: Up-regulation of miR-34a was detected in fibrosis cells. Moreover, the cellular phenotype was suppressed by miR-34a down-regulation in a primary culture of hepatic stellate cells (HSCs). Besides, it was found that increased miR-34a could significantly promote the invasion and migration of HSCs. Moreover, miR-34a activates HSCs through transforming TGF-beta, alpha-smooth muscle actin (alpha-SMA), and Monocyte chemoattractant protein-1 (MCP-1), which further affects liver fibrosis. CONCLUSIONS: MiR-34a promotes the fibrosis of HSCs as well as cell proliferation, migration, and invasion. CI - 2021 Annals of Translational Medicine. All rights reserved. FAU - Zhang, Jie AU - Zhang J AD - Department of Nutrition, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China. AD - Department of Nutrition, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China. FAU - Wang, Haixia AU - Wang H AD - Healthcare Department, The Third Hospital of Jinan, Jinan, China. FAU - Yao, Linlin AU - Yao L AD - Department of Cardiology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China. AD - Department of Cardiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China. FAU - Zhao, Peng AU - Zhao P AD - Department of Cardiology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China. AD - Department of Cardiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China. FAU - Wu, Xiaoyan AU - Wu X AD - Department of Cardiology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China. AD - Department of Cardiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China. LA - eng PT - Journal Article PL - China TA - Ann Transl Med JT - Annals of translational medicine JID - 101617978 PMC - PMC8576652 OTO - NOTNLM OT - Bifico OT - MiR-34a OT - hepatic stellate cells (HSCs) OT - liver fibrosis OT - transforming growth factor-beta (TGF-beta) COIS- Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://dx.doi.org/10.21037/atm-21-5005). The authors have no conflicts of interest to declare. EDAT- 2021/11/19 06:00 MHDA- 2021/11/19 06:01 PMCR- 2021/10/01 CRDT- 2021/11/18 07:02 PHST- 2021/07/07 00:00 [received] PHST- 2021/10/19 00:00 [accepted] PHST- 2021/11/18 07:02 [entrez] PHST- 2021/11/19 06:00 [pubmed] PHST- 2021/11/19 06:01 [medline] PHST- 2021/10/01 00:00 [pmc-release] AID - atm-09-20-1520 [pii] AID - 10.21037/atm-21-5005 [doi] PST - ppublish SO - Ann Transl Med. 2021 Oct;9(20):1520. doi: 10.21037/atm-21-5005.