2019
DOI: 10.1016/j.aohep.2019.07.007
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The regulatory role of microRNA-mRNA co-expression in hepatitis B virus-associated acute liver failure

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Cited by 8 publications
(6 citation statements)
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“…Although no studies have confirmed the relationship between RP11-488P3.1, miR-1271-5p, and ARNT2, we hypothesized that the regulatory mechanism of ARNT2 and miR-1271-5p may affect the innate immune phenotype of FGR based on the above findings. In addition, miR-3175 participates in the MAPK-related signaling pathway, whereas MAP3K9 is an upstream activator of MAPK signaling [35,36]. Choi et al also found the immunoreactivity of MAPK signaling in FGR rats [37].…”
Section: Discussionmentioning
confidence: 99%
“…Although no studies have confirmed the relationship between RP11-488P3.1, miR-1271-5p, and ARNT2, we hypothesized that the regulatory mechanism of ARNT2 and miR-1271-5p may affect the innate immune phenotype of FGR based on the above findings. In addition, miR-3175 participates in the MAPK-related signaling pathway, whereas MAP3K9 is an upstream activator of MAPK signaling [35,36]. Choi et al also found the immunoreactivity of MAPK signaling in FGR rats [37].…”
Section: Discussionmentioning
confidence: 99%
“…The idea of using molecular biomarkers instead of traditional ones for the patient's follow-up arises from the promising versatility of microRNAs during the development of chronic HBV infection. MiR-55-5p, miR-193b-5p, miR-200b-3p and miR-3175 were recently studied as molecules involved in cellular pathways such as PI3K/AKT [31] ("phosphatidylinositol-3-kinase" [32]/"protein kinase B" [33]), Ras [31] ("Rat sarcoma" [34]), MAPK [31] ("mitogen-activated protein kinase" [35]). Such pathways were related to the development of acute-on-chronic liver failure associated with HBV [31].…”
Section: Discussionmentioning
confidence: 99%
“…MiR-55-5p, miR-193b-5p, miR-200b-3p and miR-3175 were recently studied as molecules involved in cellular pathways such as PI3K/AKT [31] ("phosphatidylinositol-3-kinase" [32]/"protein kinase B" [33]), Ras [31] ("Rat sarcoma" [34]), MAPK [31] ("mitogen-activated protein kinase" [35]). Such pathways were related to the development of acute-on-chronic liver failure associated with HBV [31]. HBx downregulated the cellular expression of miR-122 in studies involving cell cultures performed on samples collected from HBV-HCC patients [36].…”
Section: Discussionmentioning
confidence: 99%
“…Thanks to this study, genes involved in the innate immune system and defense to virus were revealed. Finally, in the work by Pan et al [ 44 ], a co-expression network is constructed based on differentially-expressed microRNAs and genes identified in liver tissues from patients with hepatitis B virus (HBV). This study provides new insights on how microRNAs take part in the molecular mechanism underlying HBV-associated acute liver failure.…”
Section: Related Workmentioning
confidence: 99%