Target intelligence / Profile preview

MicroRNA 133b (miR-133b)

Target
miR-133b
Molecular classification
microRNA, Non-coding RNA, myomiR (muscle-specific microRNA)
01

Overview

MicroRNA 133b is a short (about 22 nucleotides) non-coding RNA subclassified as a muscle-specific microRNA (myomiR). It plays a critical role in the regulation of gene expression by binding to target mRNAs, usually resulting in their degradation or translation inhibition. miR-133b is highly enriched in cardiac and skeletal muscle, where it is indispensable for normal tissue development, differentiation, and structure. Abnormal miR-133b expression has been found in diverse cancers, often acting as a tumor suppressor (e.g., suppressing oncogenes like Sox9, c-MET, and WAVE2, and pathways including PI3K/AKT, MAPK, and STAT3). In some cellular contexts, it may have an oncogenic effect due to regulatory network complexity. miR-133b's regulatory impact extends to cell cycle control, apoptosis, energy metabolism (e.g., glycolysis via PKM2), and cell migration. It is under transcriptional control by various factors, including SREBP-1c and androgen receptor, and participates in metabolic and metastatic pathways crucial to cancer and muscle diseases. While not the direct target of any approved drugs, miR-133b is an active area of research for RNA therapeutics and biomarker development.

Other names
hsa-miR-133bMIRN133BmiRNA133Bmir-133bhsa-mir-133bMIR133B
02

Mechanism of action

Drugs or biologics targeting miR-133b typically act via: miRNA mimicry (supplementation of miR-133b to restore tumor suppressive function); Anti-miR oligonucleotides (inhibit endogenous miR-133b when overactivity is pathogenic); Modulation of upstream regulators impacting miR-133b expression (e.g., SREBP-1c, androgen receptor, long non-coding RNAs).

03

Biological functions

Post-transcriptional regulation of gene expression (via mRNA degradation and translation inhibition)Regulation of cell differentiation (especially in skeletal and cardiac muscle)Control of cell proliferation and migrationRegulation of apoptosis and cell deathMetabolic reprogramming in cancer cellsSuppression or promotion of metastasis, contextually dependentRegulation of muscle development and maintenance
04

Disease associations

Cancer (often acts as a tumor suppressor, occasionally as an oncogene depending on cellular context)Cardiovascular disease (key regulator of cardiac muscle development and pathology)Neurodegenerative disease (association with Parkinson's disease)Muscle disorders (including those affecting skeletal and cardiac muscle)Involvement in tongue squamous cell carcinoma and endometrial carcinoma
05

Safety considerations

Off-target effects due to broad miRNA regulatory networksPotential impact on normal muscle tissue function, given its physiological role in muscle maintenanceRisks of overexpression leading to undesirable changes in gene expression relevant to cell proliferation and apoptosis
06

Interacting drugs

Synthetic miR-133b mimics (research use)

2 more in the full profile.

07

Biomarkers

Cancer diagnosis, progression, and patient stratification (notably in breast, lung, colorectal, hepatocellular, glioma, and tongue SCC)Decision-making in muscle and cardiovascular disease prognosisMonitoring efficacy of gene therapy or miRNA-based interventions

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