Evidence map›Paper›PMID 34907156›Full record

ArticleCell death & disease2021

Long noncoding RNA GSEC promotes neutrophil inflammatory activation by supporting PFKFB3-involved glycolytic metabolism in sepsis.

Dadong Liu, Wen Sun, Danying Zhang, Zongying Yu, Weiting Qin, Yishu Liu, Kai Zhang, Jiangtao Yin

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

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  12. FOSL1-mediated LINC01566 negatively regulates CD4Journal of neuroinflammation · 2024
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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 at 2 institutions in 1 country.

Dadong Liu *Department of Critical Care Medicine, Affiliated Hospital of Jiangsu University, Zhenjiang, China.
Wen Sun *Department of Critical Care Medicine, Jurong Hospital Affiliated to Jiangsu University, Zhenjiang, China.
Danying Zhang *Department of Laboratory Medicine, Affiliated People's Hospital of Jiangsu University, Zhenjiang, China.
Zongying YuDepartment of Electrocardiograph, The No. 4 Affiliated Hospital of Jiangsu University, Zhenjiang, China.
Weiting QinState Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Shanghai Jiao Tong University, Shanghai, China.
Yishu LiuDepartment of Gastrointestinal Surgery, Affiliated Hospital of Jiangsu University, Zhenjiang, China.
Kai ZhangDepartment of Otorhinolaryngology and Head and Neck Surgery, Affiliated Hospital of Jiangsu University, Zhenjiang, China. zhangkainju@sina.com.ORCID http://orcid.org/0000-0001-9241-8137
Jiangtao YinDepartment of Critical Care Medicine, Affiliated Hospital of Jiangsu University, Zhenjiang, China. doctoryjt2438@163.com.ORCID http://orcid.org/0000-0001-5201-3397
Jiangsu University · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic reprogramming is a hallmark of neutrophil activation in sepsis. LncRNAs play important roles in manipulating cell metabolism; however, their specific involvement in neutrophil activation in sepsis remains unclear. Here we found that 11 lncRNAs and 105 mRNAs were differentially expressed in three transcriptome datasets (GSE13904, GSE28750, and GSE64457) of gene expression in blood leukocytes and neutrophils of septic patients and healthy volunteers. After Gene Ontology biological process analysis and lncRNA-mRNA pathway network construction, we noticed that GSEC lncRNA and PFKFB3 were co-expressed and associated with enhanced glycolytic metabolism. Our clinical observations confirmed the expression patterns of GSEC lncRNA and PFKFB3 genes in neutrophils in septic patients. Performing in vitro experiments, we found that the expression of GSEC lncRNA and PFKFB3 was increased when neutrophils were treated with inflammatory stimuli. Knockdown and overexpression experiments showed that GSEC lncRNA was essential for mediating PFKFB3 mRNA expression and stability in neutrophil-like dHL-60 cells. In addition, we found that GSEC lncRNA-induced PFKFB3 expression was essential for mediating dHL-60 cell inflammatory cytokine expression. Performing mechanistic experiments, we found that glycolytic metabolism with PFKFB3 involvement supported inflammatory cytokine expression. In summary, our study uncovers a mechanism by which GSEC lncRNA promotes neutrophil inflammatory activation in sepsis by supporting glycolytic metabolism with PFKFB3.

Indexed as

Neutrophil ActivationPhosphofructokinase-2RNA, Long NoncodingSepsisCytokinesGene Expression ProfilingGene Regulatory NetworksGlycolysisHumansNeutrophilsRNA, MessengerCytokinesPFKFB3 protein, humanPhosphofructokinase-2RNA, Long NoncodingRNA, Messenger

Identifiers

PMID34907156
PMCPMC8671582
OpenAlexW4200249698

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.