Evidence map›Paper›PMID 40362651›Full record

ReviewInternational journal of molecular sciences2025

Emerging Role of Long, Non-Coding RNA Nuclear-Enriched Abundant Transcript 1 in Stress- and Immune-Related Diseases.

Xingliang Liu, William Haugh, Ziqiang Zhang, Jianguo Huang

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
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

4 authors.

Xingliang LiuEarle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR 97213, USA.
William HaughEarle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR 97213, USA.
Ziqiang ZhangDepartment of Respiratory and Critical Care Medicine, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China.ORCID 0000-0001-7250-2550
Jianguo HuangEarle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR 97213, USA.ORCID 0000-0003-4777-2887

Funding

DISSECTING THE ROLES OF FAT1 AND NEAT1 IN SOFT TISSUE SARCOMA DEVELOPMENT AND METASTASIS USING NOVEL IN VIVO SARCOMA MODELSK22CA248849 · NCI · PROVIDENCE HEALTH & SERVICES - OREGON · PI HUANG, JIANGUO · 2022 to 2024
$486k
NCI NIH HHS K22 CA248849NIH HHS 5K22CA248849-03A1
6 · The paper itself

Abstract

Long, non-coding RNAs (lncRNAs) are a class of RNAs exceeding 200 nucleotides in length, lacking the ability to be translated into proteins. Over the past few decades, an increasing number of publications have established lncRNAs as potent regulators in a broad spectrum of diseases. They modulate the expression of critical genes by affecting transcription, post-transcription, translation, and protein modification. This regulation frequently involves the interaction of lncRNAs with various molecules, such as proteins, RNA, and DNA. lncRNAs are involved in diseases where stress is a significant factor. In recent years, lncRNAs have been identified as regulators of both innate and adaptive immune responses, playing significant roles in the onset and progression of diseases. Additionally, lncRNAs hold potential as biomarkers or therapeutic targets for numerous stress- and immune-related diseases. lncRNA nuclear-enriched abundant transcript 1 (NEAT1) is a notable example. This review consolidates the latest findings about the role of lncRNA NEAT1 in stress response and immune cell function in non-cancer diseases. It summarizes studies on NEAT1 regulating stress response, both innate and adaptive immunity, and its potential as a biomarker and therapeutic target for stress- and immune-related diseases.

Indexed as

Immune System DiseasesRNA, Long NoncodingStress, PhysiologicalAdaptive ImmunityAnimalsBiomarkersGene Expression RegulationHumansImmunity, InnateBiomarkersNEAT1 long non-coding RNA, humanRNA, Long Noncodingbiomarkerimmune cellsimmune-related diseaseslong, non-coding RNAsNEAT1stress-related diseasestherapeutic target

Identifiers

PMID40362651
PMCPMC12072541

What OpenQuestion holds

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Registered trials

None linked

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.