Target intelligence / Profile preview

HYOU1 antisense RNA 1 (HYOU1-AS1)

Target
HYOU1-AS1
Molecular classification
Long non-coding RNA (lncRNA), Antisense RNA, Natural antisense transcript (NAT)
01

Overview

HYOU1 antisense RNA 1 (HYOU1-AS1) is a long non-coding RNA transcribed antisense to the protein-coding gene Hypoxia Up-Regulated 1 (HYOU1). This lncRNA is highly expressed in triple-negative breast cancer (TNBC) cells and promotes tumor progression by boosting HYOU1 expression through competitive interaction with the RNA-binding protein hnRNPA1, thereby releasing post-transcriptional inhibition of HYOU1 mRNA. Knockdown of HYOU1-AS1 inhibits proliferation and migration of TNBC cells and reduces tumor formation in mice. Increased HYOU1-AS1 or HYOU1 levels are associated with poor prognosis in breast cancer, and the pathway may be considered a potential therapeutic target for future RNA-based treatments[1][3][7][8][9]. Key molecular features: - lncRNA - Antisense to HYOU1 - Regulates gene expression at the post-transcriptional level via protein (hnRNPA1) binding - Implicated in cancer biology (mainly breast cancer) - Target for RNA-based therapy research

Other names
HYOU1-AS1HYOU1-ASHYOU1 antisense RNA 1
02

Mechanism of action

Antisense oligonucleotide (ASO)-mediated inhibition or degradation of HYOU1-AS1 RNA to suppress its function Potential gene silencing, alteration of chromatin state, or interference with RNA-protein interactions

03

Biological functions

Regulation of gene expression (primarily cis-acting)Promotion of cell proliferation and migration (especially in breast cancer cells)Modulation of hypoxia response via the HYOU1 geneCompetitive binding to RNA-binding protein hnRNPA1, releasing inhibition of HYOU1 mRNA
04

Disease associations

Cancer (especially triple-negative breast cancer, TNBC)Likely involved in other tumors where HYOU1 upregulation is observedPotential roles in diseases associated with hypoxia and cellular stress (inferred from HYOU1 function)
05

Safety considerations

General ASO/lncRNA-targeting safety concerns: off-target effects, delivery to intended tissues/cells, and immune activationKnockdown of HYOU1-AS1 or HYOU1 in non-cancer cells could theoretically impair cellular protection against hypoxiaNovelty of lncRNA therapies means clinical safety profile is mostly unknown at this time
06

Interacting drugs

No directly approved drugs are known to interact with HYOU1-AS1 as of this date.

2 more in the full profile.

07

Biomarkers

HYOU1-AS1 expression may serve as a prognostic biomarker in triple-negative breast cancerHigh HYOU1-AS1 or HYOU1 levels correlate with poor breast cancer outcomesHYOU1 mRNA/protein level (as a downstream target)

Beyond the preview

Go deeper on HYOU1 antisense RNA 1 (HYOU1-AS1).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on HYOU1 antisense RNA 1 (HYOU1-AS1).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call