Target intelligence / Profile preview

MicroRNA 29c (miR-29c)

Target
miR-29c
Molecular classification
microRNA, non-coding RNA
01

Overview

MicroRNA 29c (miR-29c) is a single-stranded non-coding RNA belonging to the miR-29 family, transcribed from the MIR29C locus on chromosome 1q32.2. It is one of three closely related microRNAs (miR-29a, miR-29b, miR-29c) sharing a common seed region and similar but distinct biological roles. Functionally, miR-29c is incorporated into the RNA-induced silencing complex (RISC), where it binds target mRNAs through imperfect base pairing, leading to repression of translation or mRNA destabilization. In cancer, miR-29c often acts as a tumor suppressor; its expression is downregulated by epigenetic modifications such as promoter hypermethylation, contributing to invasiveness and chemotherapy resistance in breast cancer and hyperproduction of extracellular matrix proteins in nasopharyngeal carcinoma. In fibrotic diseases such as renal fibrosis, miR-29c is also suppressed, resulting in excess extracellular matrix production by fibroblasts and disease progression through TPM1 and Wnt/β-catenin pathway regulation. Restoration of miR-29c activity, either through hypomethylating agents or direct miRNA mimics, is under investigation as a therapeutic approach in multiple disease contexts.

Other names
hsa-mir-29cMIRN29CmiRNA29Cmir-29cMIR29C
02

Mechanism of action

Drugs elevate miR-29c expression by reducing DNA methylation in its promoter, thus restoring its tumor-suppressive and anti-fibrotic actions. Inhibition of cancer cell invasion and chemotherapy resistance by restoring miR-29c. Suppression of extracellular matrix production and fibrosis via TPM1 and Wnt/β-catenin pathway modulation.

03

Biological functions

Post-transcriptional regulation of gene expressionEpigenetic regulationRegulation of cell invasionRegulation of cell proliferationSuppression of extracellular matrix productionModulation of transcription factorsApoptosisSignal transduction
04

Disease associations

Cancer (nasopharyngeal carcinoma, breast cancer, lymphoma, general tumorigenesis)Cardiovascular disease (fibrosis)Neurodegenerative disease (Huntington disease, Alzheimer’s disease)Inflammation (immune modulation)Renal fibrosis
05

Safety considerations

Off-target effects typical of microRNA-based therapeuticsPotential for broad impact on gene expression due to multiple targetsDelivery efficiency and tissue specificity remain therapeutic challenges
06

Interacting drugs

DNA methyltransferase inhibitors (e.g., 5-aza-2'-deoxycytidine, 5-aza-CdR, which upregulate miR-29c via promoter demethylation)
07

Biomarkers

miR-29c downregulation used as a biomarker of aggressive basal-like breast cancer, renal fibrosis, and certain neurodegenerative conditionsCpG promoter methylation of miR-29c as epigenetic biomarker

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