Target intelligence / Profile preview

MicroRNA 29a (miR-29a)

Target
miR-29a
Molecular classification
MicroRNA, Non-coding RNA, Epigenetic regulator, Other
01

Overview

MicroRNA 29a (miR-29a) is a highly conserved small non-coding RNA that post-transcriptionally regulates expression of multiple genes by binding complementary sequences in the 3′ untranslated regions (UTRs) of target mRNAs, leading to their degradation or translational repression. miR-29a is part of the miR-29 family (including miR-29b and miR-29c) and is mainly transcribed from chromosome 7q32.3. It plays important roles in controlling cell proliferation, apoptosis, differentiation, and extracellular matrix remodeling, acting as a major tumor suppressor by inhibiting genes related to metastasis (e.g., CDC42, CEACAM6) and downregulating pro-fibrotic proteins such as collagens and elastin. miR-29a is frequently downregulated in diverse cancers and fibrotic conditions, and its restoration with oligonucleotide mimics is being investigated therapeutically. It also regulates immune function, angiogenesis (especially in the eye), glucose metabolism, and tissue responses to injury. Its expression levels can serve as diagnostic and predictive biomarkers. Although promising as a therapeutic target, modulation of miR-29a may challenge safety due to its broad regulatory functions across multiple tissues.

Other names
hsa-miR-29aMIR29AmiRNA29AmiR-29amicroRNA 29MIRN29AMIRN29hsa-mir-29ahsa-mir-29
02

Mechanism of action

Replacement therapy (miR-29 mimics) to restore downregulated levels in disease (e.g., fibrosis, cancer); Post-transcriptional gene silencing via targeting mRNAs coding for extracellular matrix proteins, angiogenic factors, and cell cycle regulators; Direct targeting of specific mRNA (e.g., CDC42 in NSCLC, collagens, soluble ST2)

03

Biological functions

Regulation of apoptosisRegulation of cell proliferationCell differentiationExtracellular matrix remodeling/antifibrosisAngiogenesis inhibitionMacrophage polarizationGlucose homeostasisRegulation of immune response/IL-33 signaling
04

Disease associations

Cancer (various types including non-small cell lung cancer, gastric carcinoma, osteosarcoma, glioma, colorectal cancer, pancreatic cancer, among others)Fibrotic diseases (skin, renal, cardiac, pulmonary, hepatic fibrosis, systemic sclerosis)Cardiovascular diseaseOsteoarthritis; osteoporosisAutoimmune/inflammatory diseaseOcular neovascular diseases
05

Safety considerations

Off-target effects due to broad gene regulatory rolesPotential impact on normal tissue homeostasis, wound healing, immune and metabolic functionsUndesired inhibition of physiological angiogenesis or tissue repair in nontarget tissuesLong-term effects of microRNA mimics on normal gene expression remain unknown
06

Interacting drugs

Remlarsen (MRG-201, miR-29 mimic, clinical trials for cutaneous fibrosis)

2 more in the full profile.

07

Biomarkers

Expression level of miR-29a in blood, tissues, or serum for prognosis and diagnosis (e.g., in cancer, fibrosis)miR-29a-3p as a candidate biomarker for colorectal cancer patient stratificationmiR-29a levels as a potential marker for monitoring response to miR-29-based therapies

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