Evidence map›Paper›PMID 30180891›Full record

ArticleBiological research2018

Knockdown of lncRNA MIR31HG inhibits cell proliferation in human HaCaT keratinocytes.

Jintao Gao, Fangru Chen, Mingchun Hua, Junfan Guo, Yuejuan Nong, Qinyan Tang, Fengxia Zhong, Linxiu Qin

Open access · goldAbstract read
In one paragraph

Article in Biological research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

30 citing papers in PubMed, 43 citations in OpenAlex.

  1. MIR31HG Modulates IL-4 Secretion by Keratinocytes and M2-Like Macrophage Polarization to Promote Local Immunosuppression in Condyloma Acuminata.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2026
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  15. A bibliometrics study on the status quo and hot topics of pathogenesis of psoriasis based on Web of Science.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
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  16. Signaling pathways and targeted therapies for psoriasis.Signal transduction and targeted therapy · 2023
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  19. Emerging roles of non-coding RNAs in psoriasis pathogenesis.Functional & integrative genomics · 2023
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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

8 authors at 1 institution in 1 country.

Jintao GaoCollege of Biotechnology, Guilin Medical University, Guilin, 541100, Guangxi, People's Republic of China. jintao_gao@glmc.edu.cn.ORCID http://orcid.org/0000-0002-3991-9706
Fangru ChenDepartment of Dermatology, Affiliated Hospital of Guilin Medical University, Guilin, 541001, Guangxi, People's Republic of China.
Mingchun HuaDepartment of Plastic Surgery, Affiliated Hospital of Guilin Medical University, Guilin, 541001, Guangxi, People's Republic of China.
Junfan GuoCollege of Biotechnology, Guilin Medical University, Guilin, 541100, Guangxi, People's Republic of China.
Yuejuan NongCollege of Biotechnology, Guilin Medical University, Guilin, 541100, Guangxi, People's Republic of China.
Qinyan TangCollege of Biotechnology, Guilin Medical University, Guilin, 541100, Guangxi, People's Republic of China.
Fengxia ZhongCollege of Biotechnology, Guilin Medical University, Guilin, 541100, Guangxi, People's Republic of China.
Linxiu QinCollege of Biotechnology, Guilin Medical University, Guilin, 541100, Guangxi, People's Republic of China.
Guilin Medical University · CN

Funding

Natural Science Foundation of Guangxi Zhuang Autonomous Region 2016GXNSFBA380146Project of Improving the Basic Ability of Young and Middle-aged Teachers of Guangxi Zhuang Autonomous Region KY2016YB329
6 · The paper itself

Abstract

backgroundPsoriasis is a complex, chronic inflammatory skin disease with substantial negative effects on patient quality of life. Long non-coding RNAs (lncRNAs) are able to be involved in multitudes of cellular processes in diverse human diseases. This study aimed to investigate the potential involvement of lncRNA MIR31HG in HaCaT keratinocytes proliferation.

resultsThe study showed that MIR31HG was significantly elevated in the lesional psoriatic skin compared with normal individuals' skin. Knockdown of MIR31HG inhibited HaCaT keratinocytes proliferation. Flow cytometry analysis showed that siRNA-mediated MIR31HG depletion induced cell cycle arrest in the G2/M phase. In addition, MIR31HG expression was found to be dependent on NF-κB activation.

conclusionsNF-κB activation mediated MIR31HG upregulation plays an important role in the regulation of HaCaT keratinocytes proliferation. It could be a potential diagnostic biomarker and therapeutic target for psoriasis.

Indexed as

BiomarkersCase-Control StudiesCell ProliferationGene Expression RegulationHumansKeratinocytesPsoriasisRNA, Long NoncodingSignal TransductionUp-RegulationBiomarkersRNA, Long NoncodingHaCaT keratinocytesKnockdownLncRNAMIR31HGProliferation

Identifiers

PMID30180891
PMCPMC6122774
OpenAlexW2890618663

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.