Evidence map›Paper›PMID 26395122›Full record

ArticleJournal of molecular neuroscience : MN2016

Transcriptome Sequencing to Identify Transcription Factor Regulatory Network and Alternative Splicing in Endothelial Cells Under VEGF Stimulation.

Fang Liu, Xianxin Gao, Jing Wang, Chao Gao, Xiaolin Li, Xiaodong Li, Xiao Gong, Xiandong Zeng

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

8 authors at 2 institutions in 1 country.

Fang LiuDepartment of Neurology, China Medical University, Shenyang, 110001, China.
Xianxin GaoDepartment of Neurology, Center Hospital Affiliated to Shenyang Medical College, Shenyang, 110024, China.
Jing WangDepartment of Neurology, Center Hospital Affiliated to Shenyang Medical College, Shenyang, 110024, China.
Chao GaoDepartment of Neurology, Center Hospital Affiliated to Shenyang Medical College, Shenyang, 110024, China.
Xiaolin LiDepartment of Neurology, Center Hospital Affiliated to Shenyang Medical College, Shenyang, 110024, China.
Xiaodong LiDepartment of Neurology, Center Hospital Affiliated to Shenyang Medical College, Shenyang, 110024, China.
Xiao GongDepartment of Neurology, Center Hospital Affiliated to Shenyang Medical College, Shenyang, 110024, China.
Xiandong ZengThe Dean's Office, Center Hospital Affiliated to Shenyang Medical College, Shenyang, 110024, China. zengxdxd@hotmail.com.
Shenyang Medical College · CNChina Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aims to investigate the mechanisms underlying the response of human umbilical vein vascular endothelial cells (HUVECs) to vascular endothelial growth factor (VEGF) stimulation. HUVECs were treated with or without 16 ng/mL VEGF for 4 days, and RNA was extracted from HUVECs. After sequencing and data filtering (tool: NGS QC Toolkit), clean data were mapped to genome hg19 (tool: TopHat2). Thereafter, 154 differentially expressed genes (DEGs) were identified between VEGF group and control group (tool: Cuffdiff), and DEGs were enriched in 11 pathways associated with cytokine receptor interaction and chemokine signaling. Protein-protein interaction network of DEGs was constructed (tool: STRING), and ISG15 and MX1 were hub DEGs. The regulatory network of DEGs and transcription factors (TFs) (tool: TRED database) was also constructed, and CCL2 and FN1 (hub DEGs) were co-regulated by NFKB1 and RELA (hub TFs). Moreover, exon usage and alternative splicing were analyzed (tool: DEXSeq), and the splicing of ADORA2A was altered under VEGF stimulation. VEGF might influence HUVECs proliferation and migration, as well as angiogenesis process by regulating the expression of ISG15, MX1, CCL2, FN1, and ADORA2A. However, more research studies are still required to verify these predictions.

Indexed as

Alternative SplicingGene Regulatory NetworksTranscriptomeChemokine CCL2CytokinesFibronectinsHumansHuman Umbilical Vein Endothelial CellsMyxovirus Resistance ProteinsReceptor, Adenosine A2ATranscription FactorsUbiquitinsVascular Endothelial Growth Factor ACCL2 protein, humanChemokine CCL2CytokinesFibronectinsFN1 protein, humanISG15 protein, humanMX1 protein, humanMyxovirus Resistance ProteinsReceptor, Adenosine A2ATranscription FactorsUbiquitinsVascular Endothelial Growth Factor AAlternative splicingDifferentially expressed genesHuman umbilical vein vascular endothelial cellsTranscriptome sequencingVascular endothelial growth factor

Identifiers

PMID26395122
OpenAlexW1699913131

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.