Evidence map›Paper›PMID 29282478›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2018

Tumor necrosis factor-α stimulates human amelotin gene transcription in gingival epithelial cells.

Mizuho Yamazaki, Yasunobu Iwai, Keisuke Noda, Sari Matsui, Ayako Kato, Hideki Takai, Yohei Nakayama, Yorimasa Ogata

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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 9 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 1 institution in 1 country.

Mizuho YamazakiDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Chiba, 271-8587, Japan.
Yasunobu IwaiDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Chiba, 271-8587, Japan.
Keisuke NodaDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Chiba, 271-8587, Japan.
Sari MatsuiDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Chiba, 271-8587, Japan.
Ayako KatoDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Chiba, 271-8587, Japan.
Hideki TakaiDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Chiba, 271-8587, Japan.
Yohei NakayamaDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Chiba, 271-8587, Japan.
Yorimasa OgataDepartment of Periodontology, Nihon University School of Dentistry at Matsudo, Chiba, 271-8587, Japan. ogata.yorimasa@nihon-u.ac.jp.ORCID http://orcid.org/0000-0002-2767-844X
Nihon University · JP

Funding

Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports, and Culture of Japan Scientific Research (C); No. 17K11994Nihon University Nihon University Multidisciplinary Research Grant for 2017
6 · The paper itself

Abstract

objectiveAmelotin (AMTN) is an enamel protein that is localized in the basal lamina of ameloblasts in their maturation stage and the internal basal lamina of junctional epithelium (JE) and it is suggested that AMTN could be involved in the dentogingival attachment. To elucidate the transcriptional regulation of human AMTN gene in inflamed gingiva, we have analyzed the effect of tumor necrosis factor-α (TNF-α) on the expression of AMTN gene in Ca9-22 and Sa3 human gingival epithelial cells. MATERIALS AND

methodsTotal RNAs were extracted from Ca9-22 and Sa3 cells after stimulation by TNF-α (10 ng/ml). AMTN mRNA and protein levels were measured by real-time PCR and Western blotting. Transient transfection analyses were completed using the various lengths of human AMTN gene promoter constructs with or without TNF-α. Gel mobility shift and chromatin immunoprecipitation assays were performed to investigate the transcription factors bindings to the human AMTN gene promoter by TNF-α.

resultsTNF-α (10 ng/ml) increased AMTN mRNA and protein levels after 12 h. TNF-α induced luciferase activities of human AMTN gene promoter constructs (- 211AMTN, - 353AMTN, and - 501AMTN). TNF-α-induced luciferase activities were partially inhibited in the mutation - 353AMTN constructs that included 3-bp mutations in CCAAT enhancer-binding protein 1 (C/EBP1), C/EBP2 and Ying Yang 1 (YY1) elements. Transcriptional activities induced by TNF-α were inhibited by protein kinase A, Src-tyrosine kinase, MEK1/2, p38 kinase, NF-κB, and PI3-kinase inhibitors. Gel shift assays showed that TNF-α increased nuclear proteins binding to two types of C/EBP elements (C/EBP1 and C/EBP2) and YY1 element. The results of the chromatin immunoprecipitation assays showed that C/EBPβ binding to C/EBP1 and C/EBP2, and YY1 binding to YY1 were increased by TNF-α.

conclusionsThese findings demonstrated that TNF-α stimulates AMTN gene transcription in human gingival epithelial cells via C/EBP1, C/EBP2, and YY1 elements in the human AMTN gene promoter.

Indexed as

Transcription, GeneticCell Line, TumorDental Enamel ProteinsEpithelial CellsGingivaHumansPromoter Regions, GeneticRNA, MessengerTranscription FactorsTumor Necrosis Factor-alphaAMTN protein, humanDental Enamel ProteinsRNA, MessengerTranscription FactorsTumor Necrosis Factor-alphaAmelotinGene promoterGingival epithelial cellsInflammationJunctional epitheliumTranscriptionTumor necrosis factor-α

Identifiers

PMID29282478
OpenAlexW2778026131

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.