Evidence map›Paper›PMID 40797025›Full record

ArticleScientific reports2025

Deciphering functional landscape and clinical implications of enhancer RNAs in lung adenocarcinoma.

Aike Li, Liguang Zhang, Xinsheng Du, Yi Dong, Yan Guo, Jiwei Zhao, Xiuli Fang, Pingping Lin

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Aike Li *Affiliated Hospital of Chengde Medical University, Chengde, 067000, Hebei, China.
Liguang Zhang *Affiliated Hospital of Chengde Medical University, Chengde, 067000, Hebei, China.
Xinsheng DuAffiliated Hospital of Chengde Medical University, Chengde, 067000, Hebei, China.
Yi DongAffiliated Hospital of Chengde Medical University, Chengde, 067000, Hebei, China.
Yan GuoAffiliated Hospital of Chengde Medical University, Chengde, 067000, Hebei, China.
Jiwei ZhaoAffiliated Hospital of Chengde Medical University, Chengde, 067000, Hebei, China.
Xiuli FangXinglong County People's Hospital, Chengde, 067300, Hebei, China.
Pingping LinAffiliated Hospital of Chengde Medical University, Chengde, 067000, Hebei, China. pingping0314@163.com.

Funding

Chengde Science and Technology Plan 202204A071
6 · The paper itself

Abstract

Lung adenocarcinoma (LUAD) is a common and deadly subtype of lung cancer with high mortality and limited treatment options. Enhancer RNAs (eRNAs) have emerged as important regulators in cancer biology, but their specific roles in LUAD have not been fully explored. This study aimed to investigate the role of eRNAs in LUAD pathogenesis and evaluate their potential as diagnostic biomarkers and therapeutic targets. Through integrated bioinformatics and experimental approaches, we identified differentially expressed eRNAs associated with LUAD progression. Functional analysis demonstrated that these eRNAs regulate critical pathways related to cell growth, division, repair, immune response, and tumor development. We constructed eRNA-centric regulatory networks, elucidating their interactions with transcription factors, enhancer-promoter loops, and RNA-binding proteins. Notably, eRNA ENSR00000188682 was highlighted for its central role, along with its associated transcription factor and downstream target gene ADRB2. Additionally, we developed a diagnostic prediction model based on eRNA expression profiles, which showed promising diagnostic accuracy. Our findings provide a comprehensive understanding of eRNA-mediated regulation in LUAD and suggest that eRNAs hold significant potential as prognostic biomarkers and therapeutic targets for improved clinical outcomes.

Indexed as

Adenocarcinoma of LungEnhancer Elements, GeneticLung NeoplasmsBiomarkers, TumorComputational BiologyEnhancer RNAsGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansPrognosisTranscription FactorsBiomarkers, TumorEnhancer RNAsTranscription FactorsBioinformaticsEnhancer RNAs (eRNAs)Lung adenocarcinoma (LUAD)Transcription factor (TF)

Identifiers

PMID40797025
PMCPMC12343932

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.