Target intelligence / Profile preview

MicroRNA-452-5p (miR-452-5p)

Target
miR-452-5p
Molecular classification
MicroRNA, Non-coding RNA, Regulatory RNA, Other
01

Overview

MicroRNA-452-5p (miR-452-5p) is a short, single-stranded, non-coding RNA molecule (microRNA) involved in the post-transcriptional regulation of gene expression in multicellular organisms. It regulates target gene expression by binding to complementary sequences in the 3’ untranslated region (UTR) of mRNAs, typically leading to mRNA degradation or inhibited translation. miR-452-5p is implicated in various cancers, including colorectal, liver, breast, and lung cancers, where it can act as either a tumor suppressor or promoter depending on the context. It alters key cellular processes such as proliferation, apoptosis, cell cycle progression, migration, and invasion. In colorectal and liver cancers, miR-452-5p is associated with disease progression and may serve as a biomarker or future therapeutic target[1][2][4][5][7][8]. In colorectal cancer, miR-452-5p is overexpressed in early stages, where it promotes cell proliferation (via activation of the extracellular signal-regulated kinase pathway) and inhibits EMT and invasion (through suppression of the transcription factor Slug and upregulation of E-cadherin)[1]. In hepatocellular carcinoma, miR-452-5p targets genes such as CDKN1B, contributing to oncogenic behavior[4]. It is differentially expressed in multiple cancer types and is under investigation for its diagnostic and prognostic value[5][7]. No direct small molecule or biological drugs are known to specifically target microRNA-452-5p at this time.

Other names
miR-452-5pMIR452hsa-miR-452-5p
02

Mechanism of action

Not directly targeted by drugs yet; functions through binding to the 3' untranslated region of mRNAs to induce degradation or inhibit translation of target genes[3][5].

03

Biological functions

Post-transcriptional gene regulationNegative regulation of gene expressionCell proliferationCell cycle regulationApoptosisSignal transductionEpithelial–mesenchymal transition (EMT) modulationCell invasion and migration
04

Disease associations

CancerColorectal cancerHepatocellular carcinomaLung cancerBreast cancerGliomaInflammation
05

Safety considerations

No direct safety concerns reported as therapeutic targeting is still investigationalPossible off-target effects due to broad regulatory activity if used as a drug target
06

Biomarkers

Potential biomarker for early-stage colorectal cancer[1]Potential biomarker for hepatocellular carcinoma[4]

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