Evidence map›Paper›PMID 30533429›Full record

ArticleBioMed research international2018

RNA Sequencing for Gene Expression Profiles in a Rat Model of Middle Cerebral Artery Occlusion.

Xianchun Duan, Jianghua Gan, Fan Xu, Lili Li, Lan Han, Can Peng, Qiuyu Bao, Ling Xiao, Daiyin Peng

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  5. Comprehensive Analysis of the Effect of 20(Molecules (Basel, Switzerland) · 2022
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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

9 authors at 2 institutions in 1 country.

Xianchun DuanThe First Affiliated Hospital of Anhui University of Chinese Medicine, No 117 Meishan Road, Shushan District, Hefei 230031, China.ORCID 0000-0002-1625-6700
Jianghua GanAnhui University of Chinese Medicine, No 1 Qianjiang Road, Xinzhan District, Hefei 230012, China.
Fan XuAnhui University of Chinese Medicine, No 1 Qianjiang Road, Xinzhan District, Hefei 230012, China.
Lili LiAnhui University of Chinese Medicine, No 1 Qianjiang Road, Xinzhan District, Hefei 230012, China.
Lan HanAnhui University of Chinese Medicine, No 1 Qianjiang Road, Xinzhan District, Hefei 230012, China.
Can PengAnhui University of Chinese Medicine, No 1 Qianjiang Road, Xinzhan District, Hefei 230012, China.
Qiuyu BaoChina Pharmaceutical University, No 639 Longmian Avenue, Jiangning District, Nanjing 211198, China.
Ling XiaoChina Pharmaceutical University, No 639 Longmian Avenue, Jiangning District, Nanjing 211198, China.
Daiyin PengAnhui University of Chinese Medicine, No 1 Qianjiang Road, Xinzhan District, Hefei 230012, China.ORCID 0000-0002-8734-0897
Anhui University of Traditional Chinese Medicine · CNChina Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene expression regulatory mechanisms in models of middle cerebral artery occlusion (MCAO) have been assessed in some studies, but questions remain. The discovery of differentially expressed genes (DEGs) between MCAO and control rats analyzed by next-generation RNA sequencing is of particular interest. These DEGs may help guide the clinical diagnosis of stroke and facilitate selection of the optimal treatment strategy. Twenty rats were equally divided into control and MCAO groups. Three rats from each group were randomly selected for RNA sequencing analysis. Sequence reads were obtained from an Illumina HiSeq2500 platform and mapped onto the rat reference genome RN6 using Hisat2. We identified 1,007 significantly DEGs with p<0.05, including 785 upregulated (fold change [FC]>2) and 222 downregulated (FC<0.5) DEGs, in brain tissue from MCAO rats compared with that from control rats, and numerous immune response genes were identified. Gene ontology (GO) analysis revealed that the majority of the most enriched and meaningful biological process terms were mainly involved in immune response, inflammatory response, cell activation, leukocyte migration, cell adhesion, response to external stimulus, cell migration, and response to wounding. Also enriched were immune-related pathways and neural-related pathways. Similar to GO molecular function terms, the enriched terms were mainly related to cytokine receptor activity. Six DEGs were verified by quantitative real-time polymerase chain reaction (qRT-PCR). Protein-protein interaction analysis of these hits revealed that MCAO affects complement and coagulation cascades and chemokine signaling pathway. Our study identified novel biomarkers that could help further elucidate MCAO mechanisms and processes.

Indexed as

Gene Expression ProfilingSequence Analysis, RNAAnimalsDisease Models, AnimalDown-RegulationGene OntologyInfarction, Middle Cerebral ArteryMaleProtein Interaction MapsRats, Sprague-DawleyRNA, MessengerUp-RegulationRNA, Messenger

Identifiers

PMID30533429
PMCPMC6247679
OpenAlexW2900427845

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.