Target intelligence / Profile preview

HAGLR opposite strand long non-coding RNA (HAGLROS)

Target
HAGLROS
Molecular classification
Long non-coding RNA (lncRNA), Other
01

Overview

HAGLR opposite strand long non-coding RNA (HAGLROS) is a cytoplasmic lncRNA transcript, approximately 699 nucleotides long, located on chromosome 2q31.1. It acts as a competing endogenous RNA (ceRNA), primarily by “sponging” microRNAs such as miR-100, miR-330-5p, miR-206, and miR-135b-3p, resulting in increased expression of their protein targets—including mTOR, SMARCA5, SPRR1B, NOTCH3, COL10A1, and ATG5. HAGLROS is frequently upregulated in several cancer types, where it promotes cell proliferation, migration, invasion, autophagy, and inhibits apoptosis. Its expression correlates with increased tumor grade, advanced clinical stage, metastasis, and poor patient prognosis. These findings make HAGLROS a promising molecular target and biomarker in oncology, although no approved drugs currently target it directly.

Other names
HAGLROSHOXD antisense growth-associated long-stranded noncoding RNA (antisense to HOXD, though the primary canonical name above is preferred)
02

Mechanism of action

Not directly applicable; mechanistic studies indicate its cancer-promoting effects are mediated by “sponging” microRNAs (such as miR-100, miR-330-5p, miR-206, miR-135b-3p) and influencing downstream oncogenic protein expression or mTORC1 signaling. In theory, antisense oligonucleotides or RNA interference-based therapies could downregulate HAGLROS, reversing its oncogenic effects

03

Biological functions

Cell proliferationCell migrationCell invasionAutophagy regulationApoptosis regulationImmune response (through mTORC1 pathway modulation)Cell death
04

Disease associations

Cancer (including non-small cell lung cancer, bladder cancer, breast cancer, esophageal cancer, gastric cancer, hepatocellular carcinoma, ovarian cancer, nephroblastoma, and laryngeal cancer)Drug resistance (via autophagy pathway modulation)Other (potential biomarker role for prognosis and diagnosis in multiple cancers)
05

Safety considerations

The main therapeutic challenge is targeting lncRNAs with adequate specificity and safety—off-target effects, delivery, and immune activation remain unsolved in the clinical contextAs HAGLROS is upregulated in healthy as well as cancerous tissues, silencing it might have unintended consequences (not yet documented in detail)
06

Interacting drugs

None directly listed in the available literature. HAGLROS is being investigated primarily as a molecular target and biomarker, rather than as a direct pharmacological target for existing drugs
07

Biomarkers

HAGLROS expression level can serve as a prognostic biomarker for multiple cancers, including NSCLC and bladder cancer—higher expression correlates with advanced disease/aggressive phenotype and poorer outcomes

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