Evidence map›Paper›PMID 31566109›Full record

ArticleTherapeutic advances in respiratory disease

Global transcriptional regulation of STAT3- and MYC-mediated sepsis-induced ARDS.

Jianfeng Zhang, Yifeng Luo, Xiaoling Wang, Jieyun Zhu, Qian Li, Jihua Feng, Dan He, Zhimei Zhong, Xiaowen Zheng, Junyu Lu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Therapeutic advances in respiratory disease. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

30 citing papers in PubMed, 45 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Jianfeng ZhangDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic China.
Yifeng LuoDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic China.
Xiaoling WangDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic China.
Jieyun ZhuDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic China.
Qian LiDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic China.
Jihua FengDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic China.
Dan HeDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic China.
Zhimei ZhongDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic China.
Xiaowen ZhengDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic China.
Junyu LuDepartment of Emergency, The Second Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic China.
Donghua ZouDepartment of Neurology, The Fifth Affiliated Hospital of Guangxi Medical University, No 89 Qixing Road, Nanning, Guangxi 530022, People's Republic China.ORCID 0000-0002-3891-9472
Jiefeng LuoDepartment of Neurology, The Second Affiliated Hospital of Guangxi Medical University, No 166 Daxuedong Road, Nanning, Guangxi 530007, People's Republic China.
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn recent years, sepsis-induced acute respiratory distress syndrome (ARDS) has remained a major clinical challenge for patients in intensive care units. While some progress has been reported over the years, the pathogenesis of ARDS still needs to be further expounded.

methodsIn the present study, gene set enrichment analysis, differentially expressed genes analysis, short time-series expression miner, protein-protein interaction (PPI) networks, module analysis, hypergeometric test, and functional enrichment analysis were performed in whole blood gene expression profiles of sepsis and induced-sepsis ARDS to explore the molecular mechanism of sepsis-induced ARDS.

resultsFurther dysregulated genes in the process evolving from healthy control through sepsis to sepsis-induced ARDS were identified and organized into 10 functional modules based on their PPI networks. These functional modules were significantly involved in cell cycle, ubiquitin mediated proteolysis, spliceosome, and other pathways. MYC, STAT3, LEF1, and BRCA1 were potential transcription factors (TFs) regulating these modules. A TF-module-pathway global regulation network was constructed. In particular, our findings suggest that MYC and STAT3 may be the key regulatory genes in the underlying dysfunction of sepsis-induced ARDS. Receiver operating characteristic curve analysis showed the core genes in the global regulation network may be biomarkers for sepsis or sepsis-induced ARDS.

conclusionsWe found that MYC and STAT3 may be the key regulatory genes in the underlying dysfunction of sepsis-induced ARDS.

Indexed as

Transcription, GeneticCase-Control StudiesDatabases, GeneticDisease ProgressionGene Expression RegulationGene Regulatory NetworksHumansProtein Interaction MapsProto-Oncogene Proteins c-mycRespiratory Distress SyndromeSepsisSignal TransductionSTAT3 Transcription FactorMYC protein, humanProto-Oncogene Proteins c-mycSTAT3 protein, humanSTAT3 Transcription Factoracute respiratory distress syndromesepsissepsis-induced ARDS

Identifiers

PMID31566109
PMCPMC6769203
OpenAlexW2977270190

What OpenQuestion holds

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LicenceCC BY-NC
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.