Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13699
Title: Putative salivary protein biomarkers for the diagnosis of oral lichen planus: A case-control study
Authors: Talungchit S.
Buajeeb W.
Lerdtripop C.
Surarit R.
Chairatvit K.
Roytrakul S.
Kobayashi H.
Izumi Y.
Khovidhunkit S.-O.P.
Keywords: biological marker
complement component C3c
cystatin S
fibrin degradation product
fibrinogen D fragment
protein
adult
aged
case control study
chemistry
enzyme linked immunosorbent assay
female
human
immunoblotting
lichen planus
male
mass spectrometry
middle aged
proteomics
saliva
two dimensional gel electrophoresis
Adult
Aged
Biomarkers
Case-Control Studies
Complement C3c
Electrophoresis, Gel, Two-Dimensional
Enzyme-Linked Immunosorbent Assay
Female
Fibrin Fibrinogen Degradation Products
Humans
Immunoblotting
Lichen Planus, Oral
Male
Mass Spectrometry
Middle Aged
Proteins
Proteomics
Saliva
Salivary Cystatins
Issue Date: 2018
Abstract: Background: Salivary protein biomarkers for screening and diagnosis of oral lichen planus (OLP) are not well-defined. The objective of this study was to identify putative protein biomarkers for OLP using proteomic approaches. Methods: Pooled unstimulated whole saliva was collected from five OLP patients and five healthy control participants. Saliva samples were then subjected to two-dimensional gel electrophoresis, followed by mass spectrometry to identify putative protein biomarkers. Subsequently, a subset of these putative biomarkers were validated in 24 OLP patients and 24 age-matched healthy control subjects, using an enzyme-linked immunosorbent assay (ELISA). Immunoblotting analyses were then performed in 3 pairs of age- and sex-matched OLP patients and healthy controls to confirm results from the ELISA study. Results: Thirty-one protein spots were identified, corresponding to 20 unique proteins. Notably, fibrinogen fragment D and complement component C3c exhibited increased expression in OLP patients, while cystatin SA exhibited decreased expression in OLP patients, compared with healthy control subjects. ELISA analyses indicated increased expression of fibrinogen fragment D and complement component C3c, and decreased expression of cystatin SA, in the saliva of OLP patients. Statistical differences in the expression of salivary complement C3c were observed between OLP patients and healthy control subjects. Immunoblotting analyses confirmed the results of our ELISA study. Conclusion: Complement C3c, fibrinogen fragment D and cystatin SA may serve as salivary biomarkers for screening and/or diagnosis of OLP. © 2018 The Author(s).
URI: https://ir.swu.ac.th/jspui/handle/123456789/13699
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85043468446&doi=10.1186%2fs12903-018-0504-8&partnerID=40&md5=63173c19dd6b0abe6a6b49174b02ed10
ISSN: 14726831
Appears in Collections:Scopus 1983-2021

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