Target intelligence / Profile preview

CEBPA antisense RNA 1 (CEBPA-AS1)

Target
CEBPA-AS1
Molecular classification
Long noncoding RNA (lncRNA), Enhancer RNA (eRNA), Noncoding RNA (other)
01

Overview

CEBPA antisense RNA 1 (CEBPA-AS1, also known as CEBPA divergent transcript/ADINR) is a long noncoding RNA (lncRNA) transcribed in a head-to-head orientation relative to the CEBPA gene promoter. It functions as a positive regulator (enhancer RNA or elncRNA) for CEBPA transcription, acting in cis by maintaining active enhancer marks (notably, H3K27ac) and thereby increasing CEBPA expression. CEBPA-AS1 expression is tightly correlated with CEBPA mRNA in multiple cell types, and knockdown of CEBPA-AS1 reduces both CEBPA and its downstream targets such as albumin. As CEBPA is a master regulator of cell differentiation, metabolism, and cell cycle arrest, disruption of CEBPA-AS1 is implicated in various cancers and potentially metabolic diseases. While not a direct therapeutic target, CEBPA-AS1 is a key regulatory molecule at the CEBPA locus and a prospective biomarker for enhancer function and disease state.

Other names
CEBPA divergent transcriptCEBPA-DTADINRAdipogenic differentiation induced noncoding RNACEBPA antisense RNA 1 (head to head)CEBPA antisense RNA 1 (non-protein coding)
02

Mechanism of action

Antisense oligonucleotides (ASOs): Bind and promote degradation or block function of CEBPA-DT, reducing its enhancer activity and lowering CEBPA expression. Small activating RNAs (saRNAs): May function by altering associated lncRNA expression and positively regulate CEBPA transcription.

03

Biological functions

Cis-acting positive regulation of CEBPA gene expressionModulation of cell differentiation (notably adipogenesis and potentially other lineages including hepatic and hematopoietic)Regulation of enhancer activity and chromatin state (through maintenance of H3K27ac at CEBPA enhancer)Potential role in cell cycle regulation via impact on CEBPA
04

Disease associations

Cancer, especially cancers with disrupted CEBPA function (e.g., acute myeloid leukemia, liver cancer, breast cancer, lung cancer)Possible involvement in metabolic diseases mediated by impaired adipogenesisOther, as implied by eRNA roles in enhancer dysfunction in disease
05

Safety considerations

No established clinical safety concerns, as this is not a currently drugged target.Theoretically, therapeutic manipulation of CEBPA-AS1 could affect cell proliferation and differentiation, impacting hematopoiesis or metabolic balance.Therapeutic challenge: Specificity—lncRNAs/eRNAs can have overlapping or tissue-specific roles, so off-target effects are a concern in RNA-based therapies.
06

Interacting drugs

No FDA-approved or clinical drugs known to specifically target CEBPA-AS1/CEBPA-DT/ADINR directly.

2 more in the full profile.

07

Biomarkers

Expression of CEBPA-AS1/CRED9/ADINR lncRNA as a proxy for active CEBPA gene enhancer activity, with potential application in identifying tumor subtypes or enhancer disruption.Potential biomarker in tumors exhibiting suppressed CEBPA expression and enhancer mutations.

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