Evidence map›Paper›PMID 33520437›Full record

ArticlePeerJ2021

Identification and analysis of lncRNA, microRNA and mRNA expression profiles and construction of ceRNA network in

Yueqi Li, Wudi Wei, Sanqi An, Junjun Jiang, Jinhao He, Hong Zhang, Gang Wang, Jing Han, Bingyu Liang, Li Ye and 1 more

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

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  7. DisseminatedFrontiers in cellular and infection microbiology · 2023
    Review
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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

11 authors at 1 institution in 1 country.

Yueqi Li *Guangxi Collaborative Innovation Center for Biomedicine & Guangxi-ASEAN Collaborative Innovation Center for Major Disease Prevention and Treatment, Life Science Institute, Guangxi Medical University, Nanning, Guangxi, China.
Wudi Wei *Guangxi Collaborative Innovation Center for Biomedicine & Guangxi-ASEAN Collaborative Innovation Center for Major Disease Prevention and Treatment, Life Science Institute, Guangxi Medical University, Nanning, Guangxi, China.
Sanqi AnGuangxi Collaborative Innovation Center for Biomedicine & Guangxi-ASEAN Collaborative Innovation Center for Major Disease Prevention and Treatment, Life Science Institute, Guangxi Medical University, Nanning, Guangxi, China.ORCID 0000-0002-3177-213X
Junjun JiangGuangxi Collaborative Innovation Center for Biomedicine & Guangxi-ASEAN Collaborative Innovation Center for Major Disease Prevention and Treatment, Life Science Institute, Guangxi Medical University, Nanning, Guangxi, China.
Jinhao HeGuangxi Collaborative Innovation Center for Biomedicine & Guangxi-ASEAN Collaborative Innovation Center for Major Disease Prevention and Treatment, Life Science Institute, Guangxi Medical University, Nanning, Guangxi, China.
Hong ZhangGuangxi Collaborative Innovation Center for Biomedicine & Guangxi-ASEAN Collaborative Innovation Center for Major Disease Prevention and Treatment, Life Science Institute, Guangxi Medical University, Nanning, Guangxi, China.
Gang WangGuangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health, Guangxi Medical University, Nanning, Guangxi, China.
Jing HanGuangxi Collaborative Innovation Center for Biomedicine & Guangxi-ASEAN Collaborative Innovation Center for Major Disease Prevention and Treatment, Life Science Institute, Guangxi Medical University, Nanning, Guangxi, China.
Bingyu LiangGuangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health, Guangxi Medical University, Nanning, Guangxi, China.
Li YeGuangxi Collaborative Innovation Center for Biomedicine & Guangxi-ASEAN Collaborative Innovation Center for Major Disease Prevention and Treatment, Life Science Institute, Guangxi Medical University, Nanning, Guangxi, China.
Hao LiangGuangxi Collaborative Innovation Center for Biomedicine & Guangxi-ASEAN Collaborative Innovation Center for Major Disease Prevention and Treatment, Life Science Institute, Guangxi Medical University, Nanning, Guangxi, China.
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCompetitive endogenous RNA (ceRNA) reveals new mechanisms for interactions between RNAs, which have been considered to play a significant role in pathogen-host innate immune response. However, knowledge of ceRNA regulatory networks in

methodsNext-generation sequencing technology (NGS) was used to obtain mRNA, miRNA and lncRNA expression profiles in TM-infected macrophages. The R package DESeq2 was used to identify differentially expressed lncRNA, miRNA and mRNA. The R package GOseq was used for Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, and the ceRNA network of lncRNA-miRNA-mRNA interaction was constructed in Cytoscape. Similarly, functional enrichment analysis on mRNA in the ceRNA network. Finally, two mRNAs and four lncRNAs in the ceRNA network were randomly selected to verify the expression using qRT-PCR.

resultsIn total, 119 lncRNAs, 28 miRNAs and 208 mRNAs were identified as differentially expressed RNAs in TM-infected macrophages. The constructed ceRNA network contains 38 lncRNAs, 10 miRNAs and 45 mRNAs. GO and KEGG analysis of mRNA in the ceRNA network indicated that activated pathways in TM-infected macrophages were related to immunity, inflammation and metabolism. The quantitative validation of the expression of four randomly selected differentially expressed lncRNAs, AC006252.1, AC090197.1, IL6R-AS1, LINC02009 and two mRNAs, CSF1, NR4A3 showed that the expression levels were consistent with those in the RNA-sequencing.

conclusionsThe ceRNA network related to immunity, inflammation and metabolism plays an important role in TM-macrophage interaction. This study may provide effective and novel insights for further understanding the underlying mechanism of TM infection.

Indexed as

ceRNAlncRNAMacrophageMetabolismTalaromyces marneffe

Identifiers

PMID33520437
PMCPMC7811284
OpenAlexW3120818710

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.