Evidence map›Paper›PMID 34787682›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2022

Transcriptional regulation of human odontogenic ameloblast-associated protein gene by tumor necrosis factor-α.

Yuto Tsuruya, Arisa Yamaguchi, Mizuho Yamazaki-Takai, Masaru Mezawa, Hideki Takai, Yohei Nakayama, Yorimasa Ogata

Abstract read
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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Interleukin-6 regulates humanJournal of periodontal & implant science · 2025
    Article
  2. Article
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

7 authors at 1 institution in 1 country.

Yuto TsuruyaDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Matsudo, Japan.
Arisa YamaguchiDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Matsudo, Japan.
Mizuho Yamazaki-TakaiDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Matsudo, Japan.
Masaru MezawaDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Matsudo, Japan.
Hideki TakaiDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Matsudo, Japan.
Yohei NakayamaDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Matsudo, Japan.
Yorimasa OgataDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Matsudo, Japan. ogata.yorimasa@nihon-u.ac.jp.ORCID http://orcid.org/0000-0002-2767-844X
Nihon University · JP

Funding

japan society for the promotion of science kakenhi grands 20K09945japan society for the promotion of science kakenhi grands 21K09921japan society for the promotion of science kakenhi grands 21K09922japan society for the promotion of science kakenhi grands Grant-in-Aid for Scientific Research (C)japan society for the promotion of science kakenhi grands Grant-in-Aid for Scientific Research (C) No. 18K09583japan society for the promotion of science kakenhi grands No. 17K11994japan society for the promotion of science kakenhi grands No.18K09582
6 · The paper itself

Abstract

objectiveOdontogenic ameloblast-associated protein (ODAM) is produced by maturation stage ameloblasts and junctional epithelium (JE). The function of ODAM is thought to be involved in the attachment of teeth and JE. To elucidate transcriptional regulation of human ODAM gene in inflamed gingiva, we have analyzed the effects of TNF-α on the expression of ODAM gene in Ca9-22 and Sa3 gingival epithelial cells. MATERIALS AND

methodsTotal RNAs were extracted from Ca9-22 and Sa3 cells after stimulation by TNF-α (10 ng/ml). ODAM mRNA and protein levels were analyzed by qPCR and Western blotting. Luciferase (LUC) analyses were performed using LUC constructs inserted in various lengths of ODAM gene promoter. Gel shift and chromatin immunoprecipitation (ChIP) assays were carried out.

resultsTNF-α increased ODAM mRNA and protein levels at 3 to 24 h. TNF-α induced LUC activities of the ODAM gene promoter constructs, and the activities were inhibited by protein kinase A, tyrosine kinase, MEK1/2, PI3-kinase and NF-κB inhibitors. Gel shift and ChIP assays revealed that TNF-α increased CCAAT/enhancer-binding protein (C/EBP) β and Yin Yang1 (YY1) binding to three kinds of C/EBPs and YY1 elements.

conclusionThese results demonstrate that TNF-α stimulates ODAM gene transcription via C/EBPs and YY1 elements in the human ODAM gene promoter.

Indexed as

AmeloblastsTumor Necrosis Factor-alphaEpithelial AttachmentGene Expression RegulationHumansI-kappa B ProteinsI-kappa B ProteinsTumor Necrosis Factor-alphaGene promoterHuman gingival epithelial cellsJunctional epitheliumOdontogenic ameloblast-associated proteinTNF-α

Identifiers

PMID34787682
OpenAlexW3213924889

What OpenQuestion holds

Textmetadata
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.