Evidence map›Paper›PMID 31117883›Full record

ArticleBioengineered2019

5-Aza-2'-deoxycytidine enhances lipopolysaccharide-induced inflammatory cytokine expression in human dental pulp cells by regulating TRAF6 methylation.

Zhihui Feng, Minkang Zhan, Runsha Meng, Xinxuan Wang, Qiong Xu

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2019. 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
1.3field-weighted citation impact, top 20% 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.

  1. Pooled it
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  15. PGN and LTA fromToxins · 2020
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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

5 authors at 1 institution in 1 country.

Zhihui Fenga Guanghua School of Stomatology & Guangdong Provincial Key Laboratory of Stomatology , Sun Yat-sen University , Guangzhou , China.
Minkang Zhana Guanghua School of Stomatology & Guangdong Provincial Key Laboratory of Stomatology , Sun Yat-sen University , Guangzhou , China.
Runsha Menga Guanghua School of Stomatology & Guangdong Provincial Key Laboratory of Stomatology , Sun Yat-sen University , Guangzhou , China.
Xinxuan Wanga Guanghua School of Stomatology & Guangdong Provincial Key Laboratory of Stomatology , Sun Yat-sen University , Guangzhou , China.
Qiong Xua Guanghua School of Stomatology & Guangdong Provincial Key Laboratory of Stomatology , Sun Yat-sen University , Guangzhou , China.
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dental pulp inflammation is a common bacterially driven inflammation characterized by the local accumulation of inflammatory mediators in human dental pulp. DNA methylation is a crucial epigenetic modification that that plays a fundamental role in gene transcription, and its role in inflammation-related diseases has recently attracted attention. However, its role in dental pulp inflammation is poorly understood. This study is aimed to elucidate the role of DNA methylation in lipopolysaccharide (LPS)-induced inflammatory reaction in human dental pulp cells (hDPCs). hDPCs were pretreated with DNA methylation inhibitor 5-aza-2'-deoxycytidine (5-Aza-CdR) and a cytokine antibody array was used to detect LPS-induced cytokine expression. The results indicated that 5-Aza-CdR significantly increased the expression of several pro-inflammatory cytokines in LPS-treated cells, including IL-6, IL-8, GM-CSF, MCP-2 and RANTES. The increased expression levels of IL-6 and IL-8 were further verified by qRT-PCR and ELISA. Furthermore, pretreatment with 5-Aza-CdR resulted in upregulation of p-IKKα/β, p-IκBα, p-p65 and p-ERK in the NK-κB and MAPK pathways. In addition, the 5mC level of the TRAF6 promoter was significantly decreased following 5-Aza-CdR pretreatment in the LPS-stimulated hDPCs. The findings indicate that 5-Aza-CdR significantly enhances the expression of proinflammatory cytokines and activates the NF-κB and MAPK signaling pathways by eliciting a decline in the 5mc level in the TRAF6 promoter in hDPCs, suggesting that DNA methylation may play an important role in dental pulp inflammation. This study highlights the important role of DNA methylation in the immunity defense of dental pulp infection.

Indexed as

Cells, CulturedCytokinesDecitabineDental PulpDNA MethylationHumansInflammationInterleukin-6Interleukin-8LipopolysaccharidesPromoter Regions, GeneticSignal TransductionTNF Receptor-Associated Factor 6CytokinesDecitabineInterleukin-6Interleukin-8LipopolysaccharidesTNF Receptor-Associated Factor 65-Aza-2’-deoxycytidinedental pulp cellsDNA methylationlipopolysaccharideTRAF6

Identifiers

PMID31117883
PMCPMC6550546
OpenAlexW2945424548

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.