Evidence map›Paper›PMID 34220794›Full record

ArticleFrontiers in immunology2021

Integrated Transcriptome Profiling Revealed That Elevated Long Non-Coding RNA-

Yi You, Xingwang Zhao, Yaguang Wu, Jiangming Mao, Lan Ge, Junkai Guo, Chenglei Zhao, Dong Chen, Zhiqiang Song

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

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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.

Yi YouDepartment of Dermatology, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Xingwang ZhaoDepartment of Dermatology, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Yaguang WuDepartment of Dermatology, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Jiangming MaoCenter for Genome Analysis, ABLife Inc., Wuhan, China.
Lan GeDepartment of Dermatology, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Junkai GuoDepartment of Dermatology, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Chenglei ZhaoDepartment of Dermatology, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Dong ChenCenter for Genome Analysis, ABLife Inc., Wuhan, China.
Zhiqiang SongDepartment of Dermatology, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Army Medical University · CNSouthwest Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Systemic lupus erythematosus (SLE) is a serious autoimmune disease. Its molecular pathogenesis, especially the long non-coding RNA (lncRNA) function, remains unclear. We want to investigate the lncRNA dysregulation profile and their molecular mechanisms in SLE. Methods: In this study, we analyzed the transcriptome profiles (RNA-seq) of peripheral blood mononuclear cells (PBMCs) from SLE patients and two published transcriptome datasets to explore lncRNA profiles. The differentially expressed lncRNAs were confirmed by quantitative real-time PCR in another set of female patients. We constructed the lncRNA-mRNA regulatory networks by performing weighted gene co-expression network analysis (WGCNA). Dysregulated lncRNA AC007278.2 was repressed by short hairpin RNA (shRNA) in Jurkat cells. Dual-luciferase reporter gene assay was performed to investigate the regulatory mechanism of AC007278.2 on target gene CCR7. Results: We observed dominant up-regulation of transcripts, including mRNAs and lncRNAs, in SLE patients. By WGCNA method, we identified three modules that were highly related to SLE. We then focused on one lncRNA, Conclusion: In summary, our study indicated the important regulatory role of lncRNAs in SLE.

Indexed as

AutoimmunityCell DifferentiationGene Expression ProfilingGene Expression RegulationGenetic MarkersGerminal CenterHumansJurkat CellsLupus Erythematosus, SystemicReceptors, CCR7RNA, Long NoncodingRNA, Small InterferingTh1 CellsTranscriptomeUp-RegulationCCR7 protein, humanGenetic MarkersReceptors, CCR7RNA, Long NoncodingRNA, Small InterferingCCR7lncRNAsPBMCsRNA-seqSLETfh cell differentiation

Identifiers

PMID34220794
PMCPMC8242351
OpenAlexW3165905223

What OpenQuestion holds

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LicenceCC BY
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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.