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MIR3142 host gene (MIR3142HG)

Target
MIR3142HG
Molecular classification
Long intergenic non-coding RNA (lincRNA)[1], Non-coding RNA host gene, Other (non-protein coding)
01

Overview

MIR3142 host gene (MIR3142HG) is a long intergenic non-coding RNA located on chromosome 5q33.3, generally described as the host gene for microRNAs miR-3142 and miR-146a[1][3][4][5]. While originally annotated for miR-3142, functional research indicates its predominant activity is the generation of miR-146a, a microRNA widely recognized as a negative regulator of the inflammatory response[3][4]. MIR3142HG expression is highly inducible by pro-inflammatory cytokines such as IL-1β, where it modulates the release of key inflammatory mediators (IL-8, CCL2) in fibroblasts via NF-kB signaling[3][4][5]. Differential expression and genetic variants in MIR3142HG are implicated in susceptibility to inflammatory and degenerative diseases, including IPF, acute lung injury, lumbar disc degeneration, and glioma[5]. Although not a traditional drug target, MIR3142HG serves as a critical non-coding regulatory element in inflammation and immune response networks, mainly through miR-146a-dependent mechanisms.

Other names
MIR3142 host geneMIR3142HGMIR146A host geneMIR3142HG (as commonly formatted)Host gene for miR-146a and miR-3142
02

Mechanism of action

Not applicable. Effects are mediated via the microRNAs (primarily miR-146a) produced from MIR3142HG, which can downregulate elements such as IRAK1 and TRAF6 in immune signaling networks[3].

03

Biological functions

Positive regulation of inflammatory mediator release (IL-8, CCL2)[3][4][5]Regulation of cytokine production (modulation of IL-6, IL-8, CCL2 upon IL-1β stimulation)[3][4]Regulation via NF-kB signaling pathway[4]Host gene for miR-146a, a microRNA involved in immune response and anti-inflammatory signaling[3][4][5]
04

Disease associations

Inflammatory diseases such as idiopathic pulmonary fibrosis (IPF), acute lung injury, and intervertebral disc degeneration[3][4][5]Immune response regulation[4][5]Genetic polymorphisms are associated with risk for diseases such as lumbar disc herniation, glioma, Idiopathic Pulmonary Fibrosis, and others[5]
05

Safety considerations

None directly associated, as MIR3142HG is not a pharmacological drug target[3][4][5].Therapeutic modulation of lncRNAs can present risks of off-target effects and unclear impact on downstream small RNAs.
06

Interacting drugs

None known targeting MIR3142HG directly[3][4][5]
07

Biomarkers

Several MIR3142HG single nucleotide polymorphisms (SNPs) act as biomarkers for disease susceptibility and progression, e.g. rs7727115, rs17057846, rs2961920, rs58747524 for lumbar disc herniation and glioma[5].

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