Target intelligence / Profile preview

FOXF1 adjacent non-coding developmental regulatory RNA (FENDRR)

Target
FENDRR
Molecular classification
Long non-coding RNA (lncRNA), Regulatory RNA, Chromatin-associated RNA
01

Overview

FOXF1 adjacent non-coding developmental regulatory RNA (FENDRR) is a long non-coding RNA transcribed bidirectionally from the same locus as FOXF1 and regulates gene expression through epigenetic mechanisms, including direct recruitment of chromatin-modifying complexes such as Polycomb Repressive Complex 2 (PRC2) and TrxG/MLL, and by acting as a competing endogenous RNA to sponge microRNAs and proteins that control mRNA stability. FENDRR is essential for normal organ development (heart, lungs, gastrointestinal tract) in mice and is implicated in various human diseases, including cancer (where it can act as either a tumor suppressor or an oncogene depending on cell context), fibrosis, and inflammatory conditions. Notably, altered expression of FENDRR is linked to chemotherapy resistance via modulation of drug transporter genes and transcription factors such as FOXC2, making it a candidate biomarker for prognosis and drug resistance, but not a direct druggable target.

Other names
lincFOXF1onco-lncRNA-21FOXF1-AS1FOXF1AS1TCONS_00024240FOXF1 antisense RNA 1 (head to head)FOXF1 antisense RNA 1 (non-protein coding)FENDRR
02

Mechanism of action

Not a direct drug target; for role in drug resistance: regulation of expression of drug efflux transporters (e.g., ABCC10), modulation of FOXC2/FOXL1, and influencing epigenetic silencing through chromatin modification complexes (like PRC2).

03

Biological functions

Epigenetic regulation (guides chromatin-modifying complexes to gene promoters)Competing endogenous RNA (ceRNA; sponging microRNAs and protein factors)Modulation of gene expressionRegulation of development (heart, lung, gastrointestinal tract)
04

Disease associations

Cancer (tumor suppressor or oncogenic, context-dependent)Chemotherapy resistanceFibrosisInflammatory diseases
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Safety considerations

Therapeutic modulation (upregulation/silencing) could affect crucial developmental and regulatory pathways, possibly resulting in unintended developmental or tissue maintenance effects
06

Interacting drugs

None established (FENDRR itself is not directly targeted by approved drugs; it modulates drug resistance genes and pathways)
07

Biomarkers

Low expression in non-small cell lung cancer (NSCLC) and cisplatin-resistant cells is associated with poor prognosisProposed as a prognostic biomarker in NSCLC and gastric cancer

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