Evidence map›Paper›PMID 33167868›Full record

ArticleBMC molecular and cell biology2020

Egr-1 mediates low-dose arecoline induced human oral mucosa fibroblast proliferation via transactivation of Wnt5a expression.

Qiang Chen, Jiuyang Jiao, Youyuan Wang, Zhihui Mai, Jing Ren, Sijie He, Xiaolan Li, Zheng Chen

Open access · goldAbstract read
In one paragraph

Article in BMC molecular and cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.9field-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

11 citing papers in PubMed, 14 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

8 authors at 2 institutions in 1 country.

Qiang ChenDepartment of Stomatology, the Third Affiliated Hospital of Sun Yat-sen University, No.600 Tianhe road, Guangzhou, 510630, China.
Jiuyang JiaoDepartment of Oral & Maxillofacial Surgery & Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Youyuan WangDepartment of Oral & Maxillofacial Surgery & Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Zhihui MaiDepartment of Stomatology, the Third Affiliated Hospital of Sun Yat-sen University, No.600 Tianhe road, Guangzhou, 510630, China.
Jing RenDepartment of Stomatology, the Third Affiliated Hospital of Sun Yat-sen University, No.600 Tianhe road, Guangzhou, 510630, China.
Sijie HeThe fourth people's hospital of Nanhai district of Foshan city, Foshan, China. jaccyhe@hotmail.com.
Xiaolan LiGuanghua School of stomatology & hospital of stomatology, Guangdong province key laboratory of stomatology, Sun Yat-sen University, Guangzhou, China. lixiaolan@mail.sysu.edu.cn.
Zheng ChenDepartment of Stomatology, the Third Affiliated Hospital of Sun Yat-sen University, No.600 Tianhe road, Guangzhou, 510630, China. chenzh68@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-3505-0396
Sun Yat-sen University · CNThe Fourth People's Hospital · CN

Funding

the Guangdong Provincial Natural Science Foundation 2017A030313480the Guangdong Provincial Natural Science Foundation 2019A1515011936the Guangzhou City Foundation of Science and Technology Plan 201804010015the Scientific and Technological Innovation Projects of Foshan 2017AB000612
6 · The paper itself

Abstract

backgroundArecoline is an alkaloid natural product found in the areca nut that can induce oral submucous fibrosis and subsequent development of cancer. However, numerous studies have shown that arecoline may inhibit fibroblast proliferation and prevent collagen synthesis.

resultsHigh doses of arecoline (> 32 μg/ml) could inhibit human oral fibroblast proliferation, while low doses of arecoline (< 16 μg/ml) could promote the proliferation of human oral fibroblasts. Wnt5a was found to be both sufficient and necessary for the promotion of fibroblast proliferation. Egr-1 could mediate the expression of Wnt5a in fibroblasts, while NF-κB, FOXO1, Smad2, and Smad3 did not. Treatment with siRNAs specific to Egr-1, Egr inhibitors, or Wnt5a antibody treatment could all inhibit arecoline-induced Wnt5a upregulation and fibroblast proliferation.

conclusionsEgr-1 mediates the effect of low dose arecoline treatment on human oral mucosa fibroblast proliferation by transactivating the expression of Wnt5a. Therefore, Egr inhibitors and Wnt5a antibodies are potential therapies for treatment of oral submucosal fibrosis and oral cancer.

Indexed as

ArecolineCell ProliferationCells, CulturedEarly Growth Response Protein 1FibroblastsForkhead Box Protein O1Gene Expression Regulation, NeoplasticHumansMouth MucosaOral Submucous FibrosisPromoter Regions, GeneticRNA, Small InterferingSmad2 ProteinUp-RegulationWnt-5a ProteinArecolineEarly Growth Response Protein 1EGR1 protein, humanForkhead Box Protein O1FOXO1 protein, humanRNA, Small InterferingSmad2 ProteinSMAD2 protein, humanWnt-5a ProteinWNT5A protein, humanArecolineEgr-1FibrosisOral submucous fibroblastWnt5a

Identifiers

PMID33167868
PMCPMC7653895
OpenAlexW3103273936

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.