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microRNA 196a-2 (MIR196A2)

Target
MIR196A2
Molecular classification
microRNA, non-coding RNA
01

Overview

microRNA 196a-2 is a gene-encoded, small non-coding RNA (miRNA) belonging to the Mir-196 family. In humans, it is transcribed from the MIR196A2 gene, producing a precursor that generates mature miR-196a-5p and miR-196a-3p. Mature miR-196a-2 is incorporated into the RNA-induced silencing complex (RISC), where it mediates the post-transcriptional regulation of multiple target mRNAs, including HOX gene family members and others involved in cell cycle, differentiation, and immune processes[2][4][1]. Dysregulation or genetic variation of MIR196A2 has been implicated in the pathogenesis, progression, and prognosis of numerous cancer types as well as a range of developmental and inflammatory diseases[1][3][4][5][6]. MIR196A2 variants are studied as biomarkers for clinical risk stratification and therapeutic response, although no approved drugs directly target this microRNA to date. If further disambiguation or explicit identification is needed, consult experimental databases and updated clinical trial repositories on miRNA-targeted therapies.

Other names
hsa-mir-196a-2hsa-mir-196-2MIRN196-2MIRN196A2mir-196a-2microRNA 196-2MIR196A2
02

Mechanism of action

Drugs or therapeutic modalities would act via modulation (inhibition or mimicry) of MIR196A2, influencing its suppression of target mRNAs or restoring altered regulatory networks in disease (especially cancer)[3][4][1]

03

Biological functions

Post-transcriptional regulation of gene expression[2][4]Regulation of mRNA stability and translation via RISC complex[2][4]Cell proliferation[1][5]Cell death/apoptosis[4][5]Cell differentiation[1][4]Immune response/viral immunity[1]Developmental processes[4]
04

Disease associations

Cancer (breast, lung, gastric, hepatocellular, melanoma, colorectal, prostate, glioma, esophageal, oral squamous cell carcinoma)[4][5][6]Congenital heart disease[4]Inflammation, ulcerative colitis[4]Stroke and cerebrovascular disease[4]Endometriosis[1]Keloid formation[4]Recurrent spontaneous abortion[4]
05

Safety considerations

Off-target effects due to MIR196A2's roles in fundamental processes like cell proliferation, differentiation, and apoptosis[1][4]Potential impact on developmental, inflammatory, and homeostatic pathways, raising concern for therapeutic miRNA targeting[4][1]
06

Interacting drugs

No FDA-approved drugs directly targeting MIR196A2 as of current literature; potential future therapeutic approaches through miRNA mimics/inhibitors[1][3][4]
07

Biomarkers

rs11614913 SNP in MIR196A2 precursor region for cancer susceptibility and prognosis, especially lung and breast cancer[5][6][7]MIR196A2 expression levels as prognostic biomarker, notably in hormone receptor-positive breast cancer[3][6]

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