Evidence map›Paper›PMID 26793622›Full record

ArticleFrontiers in cellular and infection microbiology2015

A Systems Biology Approach to Reveal Putative Host-Derived Biomarkers of Periodontitis by Network Topology Characterization of MMP-REDOX/NO and Apoptosis Integrated Pathways.

Fares Zeidán-Chuliá, Mervi Gürsoy, Ben-Hur Neves de Oliveira, Vural Özdemir, Eija Könönen, Ulvi K Gürsoy

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

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  9. Article
  10. Ubiquitination in Periodontal Disease: A Review.International journal of molecular sciences · 2017
    Review
  11. Article
  12. Cancer/testis antigens as molecular drug targets using network pharmacology.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    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

6 authors at 3 institutions in 4 countries.

Fares Zeidán-ChuliáPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica, Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do SulPorto Alegre, Brazil; Department of Periodontology, Institute of Dentistry, University of TurkuTurku, Finland.
Mervi GürsoyDepartment of Periodontology, Institute of Dentistry, University of Turku Turku, Finland.
Ben-Hur Neves de OliveiraPrograma de Pós-Graduação em Ciências Biológicas: Bioquímica, Departamento de Bioquímica, Instituto de Ciências Básicas da Saúde, Universidade Federal do Rio Grande do Sul Porto Alegre, Brazil.
Vural ÖzdemirFaculty of Communications and Office of the President, International Technology and Innovation Policy, Gaziantep UniversityGaziantep, Turkey; Amrita School of Biotechnology, Amrita Vishwa Vidyapeetham (Amrita University)Kollam, India.
Eija KönönenDepartment of Periodontology, Institute of Dentistry, University of TurkuTurku, Finland; Oral Health Care, Welfare DivisionTurku, Finland.
Ulvi K GürsoyDepartment of Periodontology, Institute of Dentistry, University of Turku Turku, Finland.
University of Turku · FIGaziantep University · TRUniversidade Federal do Rio Grande do Sul · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Periodontitis, a formidable global health burden, is a common chronic disease that destroys tooth-supporting tissues. Biomarkers of the early phase of this progressive disease are of utmost importance for global health. In this context, saliva represents a non-invasive biosample. By using systems biology tools, we aimed to (1) identify an integrated interactome between matrix metalloproteinase (MMP)-REDOX/nitric oxide (NO) and apoptosis upstream pathways of periodontal inflammation, and (2) characterize the attendant topological network properties to uncover putative biomarkers to be tested in saliva from patients with periodontitis. Hence, we first generated a protein-protein network model of interactions ("BIOMARK" interactome) by using the STRING 10 database, a search tool for the retrieval of interacting genes/proteins, with "Experiments" and "Databases" as input options and a confidence score of 0.400. Second, we determined the centrality values (closeness, stress, degree or connectivity, and betweenness) for the "BIOMARK" members by using the Cytoscape software. We found Ubiquitin C (UBC), Jun proto-oncogene (JUN), and matrix metalloproteinase-14 (MMP14) as the most central hub- and non-hub-bottlenecks among the 211 genes/proteins of the whole interactome. We conclude that UBC, JUN, and MMP14 are likely an optimal candidate group of host-derived biomarkers, in combination with oral pathogenic bacteria-derived proteins, for detecting periodontitis at its early phase by using salivary samples from patients. These findings therefore have broader relevance for systems medicine in global health as well.

Indexed as

ApoptosisGene Regulatory NetworksBiomarkersComputational BiologyHumansMatrix MetalloproteinasesMetabolic Networks and PathwaysNitric OxideOxidation-ReductionPeriodontitisProtein Interaction MapsProto-Oncogene MasSalivaSignal TransductionSystems BiologyBiomarkersMAS1 protein, humanMatrix MetalloproteinasesNitric OxideProto-Oncogene Mascomputational biologydrug targetgelatinasesin siliconetworkomicsoxidative stresssaliva

Identifiers

PMID26793622
PMCPMC4707239
OpenAlexW2232697138

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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.