Target intelligence / Profile preview

MicroRNA 92a-1 (MIR92A1)

Target
MIR92A1
Molecular classification
microRNA (miRNA), Non-coding RNA, miR-17/92 cluster member
01

Overview

MicroRNA 92a-1 (MIR92A1) is a highly conserved, 20–24 nucleotide non-coding RNA encoded as part of the miR-17/92 cluster, which is transcribed by RNA polymerase II, processed by Drosha and Dicer, and incorporated into the RNA-induced silencing complex (RISC). MIR92A1 regulates gene expression post-transcriptionally, influencing cell cycle, proliferation, apoptosis, angiogenesis, and differentiation. It is frequently overexpressed in various cancers and implicated in tumorigenesis, glomerular diseases, cardiovascular, immune, and neurodegenerative disorders. Circulating miR-92a levels serve as promising noninvasive biomarkers in colorectal cancer and kidney diseases. Therapeutic approaches targeting MIR92A1 focus on antisense inhibition or modulation of its upstream regulators, attracting ongoing clinical research in cancer and nephrology.

Other names
hsa-mir-92a-1hsa-mir-92-1MIRN92A1C13orf25MIRN92-1MIR-92-1MIRN92A-1miRNA92-1Putative microRNA 17 host gene proteinMIRHG1microRNA 92-1MIR17HGoncomiR-1
02

Mechanism of action

Drugs targeting microRNA 92a-1 typically act by: - Antisense inhibition (anti-miR oligonucleotides) reducing miR-92a activity and restoring expression of direct targets like tumor suppressors or CDK inhibitors, e.g., upregulating p57Kip2 to impair cell proliferation in kidney podocytes. - Modulation of miRNA-related pathways via epigenetic or RNA-editing proteins (e.g., HNRNPA2B1, METTL3).

03

Biological functions

Cell cycle regulationCell proliferationApoptosisAngiogenesisPodocyte differentiation and kidney functionRegulation of mRNA stability and translation
04

Disease associations

Cancer (colorectal, lung, lymphoma, leukemia)Renal/glomerular disease (crescentic RPGN, nephritis)Cardiovascular diseaseImmune system disordersNeurodegenerative diseaseAge-related conditions
05

Safety considerations

Therapeutic inhibition of microRNA 92a-1 may cause off-target effects in tissues where miR-92a is critical for normal cell cycle and differentiation.Broad inhibition could impact hematopoiesis or normal vascular/endothelial function.Specificity for disease-associated miR-92a upregulation versus physiological baseline remains a challenge.
06

Interacting drugs

anti-miR-92a oligonucleotides

1 more in the full profile.

07

Biomarkers

Circulating miR-92a levels in blood and stool as non-invasive biomarkers for colorectal cancer diagnosis and monitoringTissue expression of miR-92a in renal biopsies for glomerular disease severity

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