Evidence map›Paper›PMID 41154834›Full record

ArticleBiology2025

Development and Validation of a 7-eRNA Prognostic Signature for Lung Adenocarcinoma.

Yiwen Sun, Keng Chen, Jingkai Zhang, Zhijie Hu, Mingmei Xiong, Zhigang Fang, Guanmei Chen, Xiaomei Meng, Baolin Liao, Yuanyan Xiong and 1 more

Abstract read
In one paragraph

Article in Biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Yiwen SunKey Laboratory of Gene Engineering of the Ministry of Education, Department of Biochemistry, School of Life Sciences, Sun Yat-sen University, Guangzhou 510220, China.
Keng ChenGuangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou 510440, China.
Jingkai ZhangKey Laboratory of Gene Engineering of the Ministry of Education, Department of Biochemistry, School of Life Sciences, Sun Yat-sen University, Guangzhou 510220, China.
Zhijie HuKey Laboratory of Gene Engineering of the Ministry of Education, Department of Biochemistry, School of Life Sciences, Sun Yat-sen University, Guangzhou 510220, China.
Mingmei XiongGuangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou 510440, China.
Zhigang FangGuangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou 510440, China.
Guanmei ChenGuangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou 510440, China.
Xiaomei MengGuangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou 510440, China.
Baolin LiaoGuangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou 510440, China.ORCID 0009-0008-8103-1891
Yuanyan XiongKey Laboratory of Gene Engineering of the Ministry of Education, Department of Biochemistry, School of Life Sciences, Sun Yat-sen University, Guangzhou 510220, China.ORCID 0000-0002-3227-5215
Luping LinGuangzhou Eighth People's Hospital, Guangzhou Medical University, Guangzhou 510440, China.

Funding

Natural Science Foundation of Guangdong Province 2025A1515011628Science and Technology Program of Guangzhou 2025A03J4005Science and Technology Program of Guangzhou 2025A03J4006
6 · The paper itself

Abstract

Enhancer RNAs (eRNAs) are abundant in most human cells and tissues, and quantifying eRNAs has become a robust approach for biomarker discovery. While eRNAs play crucial roles in regulating biological processes and cancer progression, their functions in lung adenocarcinoma (LUAD) remain poorly understood. Here, we developed a LUAD prognostic model based on eRNA expression data from The Cancer Genome Atlas (TCGA). Through rigorous validation, a 7-eRNA signature was identified, which robustly stratified LUAD patients into high-risk and low-risk groups in both training and testing sets. Functional analyses revealed distinct enrichment of pathways related to amino acid biosynthesis, ribosome biogenesis, and proteasome activity in high-risk patients. Somatic mutation profiling highlighted TP53 and TTN as frequently mutated genes, while drug sensitivity prediction identified four potential therapeutic agents (including AZD4547 and Nutlin-3a) for high-risk individuals. Collectively, this study constructed a 7-eRNA prognostic model for LUAD, providing a powerful tool for clinical risk assessment and uncovering eRNA-mediated regulatory mechanisms.

Indexed as

drug predictioneRNALUADprognosis evaluation model

Identifiers

PMID41154834
PMCPMC12561158

What OpenQuestion holds

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Registered trials

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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.