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microRNA 4661 (MIR4661)

Target
MIR4661
Molecular classification
Non-coding RNA, microRNA
01

Overview

microRNA 4661 is a short, non-coding RNA molecule (~20–24 nucleotides) encoded by the MIR4661 gene in humans. It is transcribed by RNA polymerase II as a primary transcript, then processed by Drosha and Dicer to yield a mature miRNA that participates in the RNA-induced silencing complex (RISC). The mature miRNA binds target mRNAs via imperfect base pairing, usually resulting in translational inhibition or destabilization of the mRNA, thereby modulating gene expression. Recent research highlights miR-4661-5p, the major mature product, as a serum exosomal biomarker for early-stage hepatocellular carcinoma, with high diagnostic performance, and with potential relevance in breast cancer and possibly other conditions. No specific drugs target MIR4661 clinically, but it is being explored for its biomarker and therapeutic potential[2][3][1].

Other names
MIR4661hsa-mir-4661miR-4661miR-4661-5p
02

Mechanism of action

If drugs were to target MIR4661, anticipated mechanisms would include: - Antisense inhibition (antagomirs or anti-miRs to block function) - Mimic delivery (restoring its activity where suppressed)

03

Biological functions

Post-transcriptional gene silencingRegulation of mRNA translation and stabilityModulation of cell proliferationPotential involvement in apoptosis, metabolic processes, and signal transduction
04

Disease associations

Cancer (notably hepatocellular carcinoma, breast cancer)Potential roles in osteoporosis and bone health via related miR-466 family membersOther (by analogy to miRNAs: inflammation, metabolic disease, generally indicated for many miRNAs)
05

Safety considerations

Not directly reported for MIR4661, but general RNA-based therapies may elicit off-target effects, immune activation, or impact broader miRNA networks
06

Biomarkers

Serum exosomal miR-4661-5p: validated as a sensitive, specific biomarker for early hepatocellular carcinoma diagnosisPossibly useful in breast cancer ER+ subtype prognosis

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