Evidence map›Paper›PMID 26349411›Full record

ArticleScientific reports2015

Microarray Profiling and Co-Expression Network Analysis of LncRNAs and mRNAs in Neonatal Rats Following Hypoxic-ischemic Brain Damage.

Fengyan Zhao, Yi Qu, Junyan Liu, Haiting Liu, Li Zhang, Yi Feng, Huiqing Wang, Jing Gan, Ruifeng Lu, Dezhi Mu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. 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

10 authors at 3 institutions in 2 countries.

Fengyan ZhaoDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
Yi QuDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
Junyan LiuDepartment of Pediatrics, Binzhou Medical University Hospital, Binzhou 256600, China.
Haiting LiuDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
Li ZhangDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
Yi FengDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
Huiqing WangDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
Jing GanDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
Ruifeng LuDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
Dezhi MuDepartment of Pediatrics, West China Second University Hospital, Sichuan University, Chengdu 610041, China.
West China Second University Hospital of Sichuan University · CNSichuan University · CNBinzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) play critical roles in cellular homeostasis. However, little is known about their effect in developing rat brains with hypoxic-ischemic brain damage (HIBD). To explore the expression and function of lncRNA in HIBD, we analyzed the expression profiles of lncRNAs in hypoxic-ischemic (HI) brains and sham control using microarray analysis. The results showed a remarkable difference in lncRNA between HI and sham brains. A total of 322 lncRNAs were found to be differentially expressed in HI brains, compared to sham control. Among these, BC088414 was one of the most significantly urpregulated lncRNAs. In addition, 375 coding genes were differentially expressed between HI brains and sham control. Pathway and gene ontology analysis indicated that the upregulated coding genes mostly involved in wounding, inflammation and defense, whereas the downregulated transcripts were largely associated with neurogenesis and repair. Moreover, coding non-coding co-expression network analysis showed that the BC088414 lncRNA expression was correlated with apoptosis-related genes, including Casp6 and Adrb2. Silencing of lncRNA BC088414 in PC12 cells caused reduced mRNA level of Casp6 and Adrb2, decreased cell apoptosis and increased cell proliferation. These results suggested lncRNA might participate in the pathogenesis of HIBD via regulating coding genes.

Indexed as

Gene Expression ProfilingGene Expression RegulationGene Regulatory NetworksTranscriptomeAnimalsAnimals, NewbornApoptosisCell ProliferationCluster AnalysisComputational BiologyGene Knockdown TechniquesGene OntologyHypoxia-Ischemia, BrainOpen Reading FramesRatsReproducibility of ResultsRNA, Long NoncodingRNA, Messenger

Identifiers

PMID26349411
PMCPMC4563552
OpenAlexW1461724045

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.