Target intelligence / Profile preview

Long intergenic non-protein coding RNA 839 (LINC00839)

Target
LINC00839
Molecular classification
Long non-coding RNA, Other
01

Overview

Long intergenic non-protein coding RNA 839 (LINC00839) is a human long non-coding RNA (lncRNA) located on chromosome 10 and transcribed in the forward strand[3][7]. LINC00839 does not encode a protein but exerts regulatory functions, mainly in cancer biology. It is widely upregulated in several tumor types (osteosarcoma, lung adenocarcinoma, liver cancer, colorectal cancer, neuroblastoma, and nasopharyngeal carcinoma)[1][2][4][6][8]. Functionally, LINC00839 promotes malignant characteristics such as cell proliferation, migration, invasion, and metabolic reprogramming, often by acting as a microRNA sponge or interacting with regulatory proteins in the nucleus or cytoplasm. It contributes to the activation of oncogenic pathways, such as the NF-κB axis and the c-Met pathway, and modulates key cellular behaviors associated with tumor progression and metastasis[2][4]. LINC00839 is considered both as a putative therapeutic target and a biomarker candidate for cancer prognosis and therapy-monitoring, though no drugs are yet directly targeting it in clinical use[4].

Other names
LINC00839
02

Mechanism of action

Acts as a competitive endogenous RNA (ceRNA) by sponging microRNAs such as miR-454-3p and miR-17-5p, thereby de-repressing targets like c-Met and TLR4[1][2][4]. Binds proteins such as PTBP1 to regulate nuclear translocation of NF-κB p65 and thus modulate transcription of target genes[2]. Interacts with proteins involved in metabolism and RNA transport (e.g., FMNL2 in hepatocellular carcinoma)[6]. Regulates cellular signaling pathways including NF-κB and TLR4/NF-κB axes[2].

03

Biological functions

Cell proliferationCell migrationCell invasionEpithelial-mesenchymal transition (EMT)Apoptosis suppressionRegulation of NF-κB signalingceRNA activity (microRNA sponge)Regulation of gene expression in nucleus and cytoplasmPromotion of glycolysis (metabolic reprogramming)
04

Disease associations

CancerOsteosarcomaLung adenocarcinomaHepatocellular carcinoma (liver cancer)Colorectal cancerNeuroblastomaNasopharyngeal carcinoma
05

Safety considerations

As a non-coding RNA target, challenges include delivery and specificity of RNA-targeted therapeuticsLack of direct drug modulators; current strategies are limited to gene silencing or antisense technologies[4]
06

Biomarkers

Potential prognostic biomarker in multiple cancers, where high expression is associated with a poorer survival (e.g., osteosarcoma, neuroblastoma, hepatocellular carcinoma)[1][6][8]

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