Literature DB >> 29610270

Targeted Proteomics Guided by Label-free Quantitative Proteome Analysis in Saliva Reveal Transition Signatures from Health to Periodontal Disease.

Nagihan Bostanci1, Nathalie Selevsek2, Witold Wolski2, Jonas Grossmann2, Kai Bao3, Asa Wahlander4, Christian Trachsel2, Ralph Schlapbach2, Veli Özgen Öztürk5, Beral Afacan5, Gulnur Emingil6, Georgios N Belibasakis3.   

Abstract

Periodontal diseases are among the most prevalent worldwide, but largely silent, chronic diseases. They affect the tooth-supporting tissues with multiple ramifications on life quality. Their early diagnosis is still challenging, due to lack of appropriate molecular diagnostic methods. Saliva offers a non-invasively collectable reservoir of clinically relevant biomarkers, which, if utilized efficiently, could facilitate early diagnosis and monitoring of ongoing disease. Despite several novel protein markers being recently enlisted by discovery proteomics, their routine diagnostic application is hampered by the lack of validation platforms that allow for rapid, accurate and simultaneous quantification of multiple proteins in large cohorts. Here we carried out a pipeline of two proteomic platforms; firstly, we applied open ended label-free quantitative (LFQ) proteomics for discovery in saliva (n = 67, including individuals with health, gingivitis, and periodontitis), followed by selected-reaction monitoring (SRM)-targeted proteomics for validation in an independent cohort (n = 82). The LFQ platform led to the discovery of 119 proteins with at least 2-fold significant difference between health and disease. The 65 proteins chosen for the subsequent SRM platform included 50 functionally related proteins derived from the significantly enriched processes of the LFQ data, 11 from literature-mining, and four house-keeping ones. Among those, 60 were reproducibly quantifiable proteins (92% success rate), represented by a total of 143 peptides. Machine-learning modeling led to a narrowed-down panel of five proteins of high predictive value for periodontal diseases with maximum area under the receiver operating curve >0.97 (higher in disease: Matrix metalloproteinase-9, Ras-related protein-1, Actin-related protein 2/3 complex subunit 5; lower in disease: Clusterin, Deleted in Malignant Brain Tumors 1). This panel enriches the pool of credible clinical biomarker candidates for diagnostic assay development. Yet, the quantum leap brought into the field of periodontal diagnostics by this study is the application of the biomarker discovery-through-verification pipeline, which can be used for validation in further cohorts.
© 2018 Bostanci et al.

Entities:  

Keywords:  Biofluids*; Biomarker: Diagnostic; Biomarker: Prognostic; Diagnostic; Host-Pathogen Interaction; Infectious disease; Inflammation; Inflammatory response; Label-free quantification; Selected reaction monitoring; agressive periodontitis; chronic periodontitis; oral biofluids; periodontal disease; saliva

Mesh:

Substances:

Year:  2018        PMID: 29610270      PMCID: PMC6030726          DOI: 10.1074/mcp.RA118.000718

Source DB:  PubMed          Journal:  Mol Cell Proteomics        ISSN: 1535-9476            Impact factor:   5.911


  80 in total

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4.  Salivary lactoferrin and low-Mr mucin MG2 in Actinobacillus actinomycetemcomitans-associated periodontitis.

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5.  Molecular evolution of enolase.

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6.  Novel protein identification methods for biomarker discovery via a proteomic analysis of periodontally healthy and diseased gingival crevicular fluid samples.

Authors:  Richard C Baliban; Dimitra Sakellari; Zukui Li; Peter A DiMaggio; Benjamin A Garcia; Christodoulos A Floudas
Journal:  J Clin Periodontol       Date:  2011-11-10       Impact factor: 8.728

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Journal:  Biochim Biophys Acta       Date:  2007-05-10

Review 8.  Cysteine peptidases of mammals: their biological roles and potential effects in the oral cavity and other tissues in health and disease.

Authors:  D P Dickinson
Journal:  Crit Rev Oral Biol Med       Date:  2002

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10.  Trafficking and postsecretory events responsible for the formation of secreted human salivary peptides: a proteomics approach.

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Journal:  Mol Cell Proteomics       Date:  2008-01-09       Impact factor: 5.911

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3.  Pressure Cycling Technology Assisted Mass Spectrometric Quantification of Gingival Tissue Reveals Proteome Dynamics during the Initiation and Progression of Inflammatory Periodontal Disease.

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7.  Automated Pre-Analytic Processing of Whole Saliva Using Magnet-Beating for Point-of-Care Protein Biomarker Analysis.

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8.  A salivary metabolite signature that reflects gingival host-microbe interactions: instability predicts gingivitis susceptibility.

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9.  Salivary proteotypes of gingivitis tolerance and resilience.

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