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MicroRNA 30a (miR-30a)

Target
miR-30a
Molecular classification
MicroRNA, Non-coding RNA, RNA gene
01

Overview

MicroRNA 30a (miR-30a) is a highly conserved, small non-coding RNA (18–25 nucleotides) belonging to the miR-30 family, encoded by the MIR30A gene on chromosome 6q.13[1][6]. It acts as a post-transcriptional regulator of gene expression by binding to complementary sequences in the 3′ untranslated regions of target mRNAs, leading to translational repression or mRNA degradation. miR-30a participates in key biological processes including cell cycle regulation, apoptosis, inhibition of cell migration and invasion, autophagy control, and EMT. Functionally, miR-30a is generally considered a tumor suppressor in a range of cancers by downregulating target genes such as TM4SF1, CD73, IGF1R, and BECLIN-1, thereby inhibiting tumor progression, metastasis, and drug resistance[1][2][4][5]. It also plays a role in metabolic homeostasis and inflammation, with reduced expression associated with poor outcomes in metabolic and autoimmune diseases. Because of its dysregulation in disease, miR-30a is under investigation as both a biomarker and a therapeutic target[1][3][6].

Other names
hsa-mir-30aMIR30AMIRN30Amir-30a
02

Mechanism of action

Modulation of miR-30a expression (e.g., overexpression or mimic administration) suppresses oncogene or fibrosis-related target genes at the mRNA level, primarily through translational repression or mRNA destabilization

03

Biological functions

Regulation of gene expressionCell cycle controlApoptosisCell proliferationCell migration and invasionEpithelial-mesenchymal transition (EMT)Autophagy
04

Disease associations

Cancer (including colon, breast, ovarian, gastric, and hepatocellular cancers)Cardiovascular disease (via fibrosis and cell response in obesity)Inflammation (including roles in lupus nephritis and glomerular disease)Metabolic disease/obesity
05

Safety considerations

Modulation of microRNA levels may have widespread effects due to regulation of multiple targets; off-target or unintended biological effects are a key challenge.Delivery and stability of miRNA-based therapies require careful optimization to avoid immune activation or systemic toxicity.
06

Interacting drugs

No small-molecule drugs or conventional pharmaceuticals directly interact with microRNA 30a as of current knowledge; however, gene therapy approaches (such as miRNA mimics or antagonists) and viral delivery (e.g., adenovirus expressing miR-30a) are being investigated in preclinical research
07

Biomarkers

Downregulation of miR-30a in tumor tissues (biomarker of cancer progression/aggressiveness)miR-30a levels in adipose tissue as a biomarker for insulin sensitivity and metabolically healthy obesity

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