Target intelligence / Profile preview

MicroRNA 379 (MIR379)

Target
MIR379
Molecular classification
microRNA, non-coding RNA, post-transcriptional regulator
01

Overview

MicroRNA 379 (MIR379) is a non-coding RNA molecule encoded by the MIR379 gene located on chromosome 14q32.31[1][3]. It is part of the large miR-379/656 cluster, one of the largest and most differentially regulated miRNA clusters in the human genome[2][5]. miR-379 is processed into a mature, ~22-nucleotide RNA that acts as a post-transcriptional regulator of gene expression, influencing the stability and translation of numerous mRNA targets[3]. It plays essential biological roles including tumor suppression, regulation of apoptosis, and modulation of metabolic and cardiovascular processes. miR-379 has been implicated in the pathogenesis of cancers (especially breast and brain cancer), diabetic kidney disease, cardiomyopathy, and neuromuscular diseases[1][2][3][5]. Its dysregulation is a diagnostic and prognostic biomarker in cancer, and it is being investigated as a potential therapeutic target through anti-miR or mimic approaches. It mediates effects through direct binding to 3'-UTR sites in key target mRNAs like Smurf1 and EDEM3, thus influencing pathways related to cell cycle, DNA repair, mitochondrial function, and cell death[1][5].

Other names
hsa-mir-379MIRN379mir-379MIR379miR-379miR-379-5p
02

Mechanism of action

Target for oligonucleotide inhibitors (antagomirs, anti-miRs). Potential use of mimics for miRNA replacement therapies.

03

Biological functions

Regulation of gene expression at the post-transcriptional levelApoptosis regulationCell cycle regulationTumor suppressionRegulation of endoplasmic reticulum (ER) stressModulation of immune cell function (e.g., CD8+ T cell exhaustion)
04

Disease associations

Cancer (various types, including breast cancer, glioblastoma, melanoma, gastrointestinal tumors, ovarian cancer)Cardiovascular disease (e.g., heart failure associated with Klotho deficiency)Diabetic kidney diseaseInflammatory and metabolic diseasesNeuromuscular diseases (e.g., polymyositis, facioscapulohumeral muscular dystrophy 1)
05

Safety considerations

Off-target effects of miRNA-based therapiesChallenges in delivery and stability of miRNA therapeuticsPotential for broad-ranging effects due to the regulation of multiple target genes
06

Biomarkers

Diagnostic and prognostic biomarker in breast cancer and glioblastomaMarker for diabetic kidney disease severityPossible stratification biomarker for subtypes of breast cancer (e.g., Basal and Luminal B)

Beyond the preview

Go deeper on MicroRNA 379 (MIR379).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on MicroRNA 379 (MIR379).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call