Target intelligence / Profile preview

PRC2 and DDX5 associated long noncoding RNA (PRADX)

Target
PRADX
Molecular classification
Long noncoding RNA (lncRNA), Epigenetic regulator, Other
01

Overview

PRC2 and DDX5 associated long noncoding RNA (PRADX) is a nuclear long noncoding RNA highly expressed in glioblastoma and colon adenocarcinoma tissues. It acts as a cancer driver by recruiting the PRC2/DDX5 complex to chromatin, specifically increasing H3K27me3 at the UBXN1 gene promoter, thereby silencing UBXN1 and activating the NF-κB and STAT3 oncogenic pathways. PRADX is transcriptionally upregulated by the RUNX1-CBFβ complex, is predominantly localized in the cell nucleus, and its knockdown suppresses tumor cell viability and tumorigenesis in preclinical models. High PRADX expression is associated with worse outcomes, particularly in mesenchymal glioblastoma, making it a potential therapeutic target and a biomarker for aggressive tumor subtypes.

Other names
ENST00000449248.1
02

Mechanism of action

Recruitment of Polycomb repressive complex 2 (PRC2) and DEAD-box helicase 5 (DDX5) to gene promoters (notably UBXN1), resulting in trimethylation of histone H3 at lysine 27 (H3K27me3) and transcriptional repression. Activation of NF-κB signaling via UBXN1 silencing. Activation of STAT3 pathway via suppression of BLCAP (as shown in glioblastoma models).

03

Biological functions

Epigenetic regulation (regulation of histone methylation through recruitment of PRC2/DDX5 complex)Gene silencing (of targets such as UBXN1)Activation of oncogenic pathways (e.g., NF-κB, STAT3)Promotion of cell proliferationCell cycle regulationRegulation of cell metabolism
04

Disease associations

Cancer (glioblastoma, colon adenocarcinoma, especially mesenchymal GBM)Tumor progression
05

Safety considerations

Potential off-target effects for lncRNA-targeted therapiesSpecificity and delivery challenges for RNA-targeted drugsUnknown long-term safety profile for PRADX-directed interventions
06

Interacting drugs

No direct drugs currently targeting PRADX reported; however, pathway inhibitors such as ACSL1 and CPT1 inhibitors have been proposed in combination with PRADX modulation in GBM models

1 more in the full profile.

07

Biomarkers

High PRADX expression as a biomarker for poor prognosis in glioblastoma and colon adenocarcinomaPRADX expression as a biomarker for mesenchymal glioblastoma subtype

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