Evidence map›Paper›PMID 36943641›Full record

ArticleInflammation2023

Long Non-Coding RNA-GDA-1 Promotes Keratinocyte Proliferation and Psoriasis Inflammation by Regulating the STAT3/NF-κB Signaling Pathway via Forkhead Box M1.

Xueqing Li, Fuqiang Chen, Jiaoying Ju, Xiran Yin, Zhenxian Yang, Zhengjun Li, Qing Sun

Abstract read
PubMed Publisher
In one paragraph

Article in Inflammation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Role of the STAT3 Signaling Pathway in Cell Proliferation and Inflammation in Psoriasis and Approaches for Targeted Therapies: A Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Review
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  7. Key genes and immune infiltration patterns and the clinical implications in psoriasis patients.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
    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

7 authors at 3 institutions in 1 country.

Xueqing Li *Department of Dermatology, Qilu Hospital, Shandong University, Jinan, 250012, Shandong, China.
Fuqiang Chen *Department of Dermatology, Qilu Hospital, Shandong University, Jinan, 250012, Shandong, China.
Jiaoying JuDepartment of Dermatology, Qilu Hospital, Shandong University, Jinan, 250012, Shandong, China.
Xiran YinDepartment of Dermatology, Hospital of Weifang People, Weifang, Shandong, People's Republic of China.
Zhenxian YangDepartment of Dermatology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Zhengjun LiDepartment of Dermatology, Qilu Hospital, Shandong University, Jinan, 250012, Shandong, China. Lzj19861126@163.com.
Qing SunDepartment of Dermatology, Qilu Hospital, Shandong University, Jinan, 250012, Shandong, China. sunqing7226@163.com.
Qilu Hospital of Shandong University · CNShandong Provincial Hospital · CNWeifang People's Hospital · CN

Funding

National Natural Science Foundation of China 81972937National Science and Technology Major Project 2017YFA0104604
6 · The paper itself

Abstract

Psoriasis is a chronic inflammatory skin disease associated with multiple comorbidities and complex pathogenesis. Long non-coding RNAs (lncRNAs) play an important regulatory role in many diseases, including psoriasis. In this study, We aimed to investigate the role and mechanism of lncRNA GDA-1 (GDA) in M5-treated psoriatic keratinocytes. GDA expression was significantly upregulated in psoriatic tissues and M5-treated keratinocytes. By silencing and overexpressing GDA in NHEKs and Ker-CT cells, we showed that GDA regulated proliferation and cell cycle and increased secretion of interleukin-1β (IL-1β), IL-6, and chemokine ligands 2 and 20 (CCL2 and CCL20). RNA sequencing after GDA silencing led to the identification of a close regulatory relationship between GDA and Forkhead Box M1 (FOXM1). GDA significantly influenced FOXM1 expression at both mRNA and protein levels and activated STAT3/NF-κB signaling pathways. STAT3 and NF-κB inhibition abrogated GDA effects on keratinocyte proliferation and inflammation. In conclusion, our study is the first to report that Lnc-GDA-1 distinctly regulates FOXM1 expression and mediates proliferation and inflammation of psoriatic keratinocytes through the STAT3/NF-κB signaling pathway, which may be a potent target for psoriasis treatment.

Indexed as

PsoriasisRNA, Long NoncodingCell ProliferationHumansInflammationKeratinocytesNF-kappa BSignal TransductionSTAT3 Transcription FactorNF-kappa BRNA, Long NoncodingSTAT3 protein, humanSTAT3 Transcription FactorFOXM1inflammationLnc-GDA-1proliferationpsoriasis.

Identifiers

PMID36943641
OpenAlexW4328048154

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.