Target intelligence / Profile preview

RARA antisense RNA 1 (RARA-AS1)

Target
RARA-AS1
Molecular classification
Long non-coding RNA, Antisense RNA, Other
01

Overview

RARA antisense RNA 1 (RARA-AS1) is a long non-coding antisense RNA with elevated expression in various human cancers, most notably glioblastoma, and plays key roles in regulating cell proliferation, invasion, and migration[2][4][7]. Functional studies demonstrate that knockdown of RARA-AS1 reduces tumor cell proliferation and migration, highlighting its significance in tumor progression. RARA-AS1 is highly correlated with immune checkpoint markers, mismatch repair genes, and participates in oncogenic and immune-related pathways. It is considered both a potential therapeutic target and prognostic biomarker, particularly in glioblastoma and other malignancies[2][4][7]. No direct drug is currently known to interact with RARA-AS1, but it is a subject for further drug discovery efforts, including RNA-based therapies[2].

Other names
CTD-2267D19.2RARA-AS1
02

Mechanism of action

RARA-AS1's mechanism involves RNA binding protein interaction (e.g., CSTF2T-mediated axis). It regulates oncogenic pathways such as cell cycle, P53 pathway, nucleotide metabolism, estrogen signaling, and ubiquitin-mediated proteolysis. Furthermore, it modulates immune checkpoint genes and has potential as a target for antisense RNA therapeutics through oligonucleotide-mediated knockdown.

03

Biological functions

Regulation of gene expressionCell proliferationCell migrationCell invasionImmune modulationOther
04

Disease associations

CancerGlioblastomaPrognostic marker (pan-cancer)Immune dysregulation (sepsis)Other
05

Safety considerations

None specifically reported; general challenges may include targeting lncRNAsOff-target effects of antisense therapeuticsUnclear clinical applicability
06

Biomarkers

Prognostic biomarker for overall and disease-specific survival in cancers (notably glioblastoma)Marker of poor prognosis when highly expressed in several tumor types

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