Evidence map›Paper›PMID 34059095›Full record

ArticleJournal of translational medicine2021

MAPK14 over-expression is a transcriptomic feature of polycythemia vera and correlates with adverse clinical outcomes.

Chao Guo, Ya-Yue Gao, Qian-Qian Ju, Min Wang, Chun-Xia Zhang, Ming Gong, Zhen-Ling Li

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2021. 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
0.3field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

7 authors at 1 institution in 1 country.

Chao GuoDepartment of Hematology, China-Japan Friendship Hospital, Yinghua East Street, Beijing, China.
Ya-Yue GaoDepartment of Hematology, China-Japan Friendship Hospital, Yinghua East Street, Beijing, China.
Qian-Qian JuDepartment of Hematology, China-Japan Friendship Hospital, Yinghua East Street, Beijing, China.
Min WangDepartment of Hematology, China-Japan Friendship Hospital, Yinghua East Street, Beijing, China.
Chun-Xia ZhangDepartment of Hematology, China-Japan Friendship Hospital, Yinghua East Street, Beijing, China.
Ming GongDepartment of Hematology, China-Japan Friendship Hospital, Yinghua East Street, Beijing, China.
Zhen-Ling LiDepartment of Hematology, China-Japan Friendship Hospital, Yinghua East Street, Beijing, China. lizhenling03@163.com.ORCID 0000-0002-6623-1683
China-Japan Friendship Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe transcriptomic signature has not been fully elucidated in PV, as well as mRNA markers for clinical variables (thrombosis, leukemic transformation, survival, etc.). We attempted to reveal and validate crucial co-expression modules and marker mRNAs correlating with polycythemia vera (PV) by weighted gene co-expression network analysis (WGCNA). MATERIAL AND

methodsThe GSE57793/26014/61629 datasets were downloaded from Gene Expression Omnibus (GEO) database and integrated into one fused dataset. By R software and 'WGCNA' package, the PV-specific co-expression module was identified, the pathway enrichment profile of which was obtained by over-representation analysis (ORA). Protein-protein interaction (PPI) network and hub gene analysis identified MAPK14 as our target gene. Then the distribution of MAPK14 expression in different disease/mutation types, were depicted based on external independent datasets. Genome-scale correlation analysis revealed the association of MAPK14 and JAK/STAT family genes. Then gene set enrichment analysis (GSEA) was performed to detect the activated and suppressed pathways associating with MAPK14 expression. Moreover, GSE47018 dataset was utilized to compare clinical variables (thrombosis, leukemic transformation, survival, etc.) between MAPK14-high and MAPK14-low groups.

resultsAn integrated dataset including 177 samples (83 PV, 35 ET, 17 PMF and 42 normal donors) were inputted into WGCNA. The 'tan' module was identified as the PV-specific module (R

conclusionMAPK14 over-expression was identified as a transcriptomic feature of PV, which was also related to inferior clinical outcomes. The results provided novel insights for biomarkers and therapeutic targets for PV.

Indexed as

Mitogen-Activated Protein Kinase 14Polycythemia VeraThrombocythemia, EssentialHumansPhosphatidylinositol 3-KinasesTranscriptomeMitogen-Activated Protein Kinase 14Phosphatidylinositol 3-KinasesExpressionMAPK14Polycythemia veraWGCNA

Identifiers

PMID34059095
PMCPMC8166116
OpenAlexW3164260273

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.