Target intelligence / Profile preview

microRNA 676 (MIR676)

Target
MIR676
Molecular classification
MicroRNA, Non-coding RNA, Gene regulator
01

Overview

microRNA 676 (MIR676) is a conserved small non-coding RNA functioning as a post-transcriptional regulator of gene expression. It is involved in critical cellular processes including cell proliferation, apoptosis, neuroprotection, and metabolic regulation. In cancer, MIR676 expression is closely associated with tumor phenotype and can sensitize cells to chemotherapeutic agents, such as metformin, by promoting apoptosis and cell cycle arrest. Its neuroprotective role is linked to antiapoptotic activity following brain injury. MIR676 acts through base pairing with target mRNAs for gene silencing, and its regulatory impact may be modulated by proteins such as p53. Dysregulation of MIR676 is implicated in various diseases, most notably cancer and neurological disorders, making it a candidate biomarker and potential therapeutic target.

Other names
hsa-mir-676mir-676MIR676rno-miR-676-1mmu-mir-676miR-676-3p
02

Mechanism of action

Gene silencing via binding to 3′UTR of target mRNA, leading to repression or degradation. Cooperativity: miRNAs can synergize via TNRC6 proteins for stronger repression. Drug sensitization: miR-676-3p increases cell sensitivity to metformin via apoptosis and cell cycle arrest.

03

Biological functions

Post-transcriptional regulation of gene expressionRegulation of cell proliferationApoptosis (promotes or suppresses depending on context)Cell cycle arrestSensitization to metabolic drugs (metformin)Neuroprotection (antiapoptotic role in neuroprotection after brain injury in rats)
04

Disease associations

Cancer (downregulation in signet-ring cell carcinoma of gastric cancer correlates with aggressive phenotype; involvement in colorectal cancer cell metabolism)Neurological disease (regulation by p53 in neuroblastoma; neuroprotective effects in ischemia models)Potential role in metabolic disease (modulation of response to metformin)
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Safety considerations

Not directly reported; microRNAs may regulate many genes, so therapeutic manipulation could have broad pleiotropic effects (general safety concern for miRNA targeting)Off-target effects and impact on complex regulatory networks typical for miRNAs
06

Interacting drugs

Metformin
07

Biomarkers

Lower expression level in signet-ring cell gastric carcinoma as a potential biomarker for aggressive phenotypeExpression profile in neuroblastoma and in ischemia-injured brain tissue as a marker of p53 regulation and neuroprotective response

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