Chun Yao , Haiyan Xin , Si Liu , Hong Wang , Yanhong Ma , Chao Yao , Jian Meng
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引用次数: 0
Abstract
Objectives
This study aims to explore whether Connexin 43 (Cx43) in salivary extracellular vesicles (EVs) can serve as a biomarker for diagnosing oral lichen planus (OLP), an inflammatory oral mucosal disorder.
Design
The study assessed disease activity in OLP patients using the reticulum-erosion-ulcer disease activity score. Saliva EVs were isolated and purified with an EV Enrichment Kit. Transmission electron microscopy was used to examine the morphology and size of EVs, while Western blotting verified EV biomarkers. ELISA measured serum inflammatory factors, such as TNF-α and IL-17. The importance of Cx43 in the diagnosis of OLP was evaluated using receiver operating characteristic (ROC) curve analysis, and correlations were determined through Pearson analysis.
Results
The average diameter of isolated saliva EVs was approximately 110 nm, and they expressed high levels of known EV biomarkers. In OLP patients, both Cx43 mRNA and protein levels were significantly higher compared to healthy controls. Furthermore, Cx43 mRNA and protein levels increased gradually with increased disease severity, from the reticular type to the more severe erosion type of OLP. Cx43 mRNA and protein levels were found to effectively diagnosing OLP and correlated significantly with disease activity scores. Moreover, elevated Cx43 mRNA and protein levels showed strong positive correlations with serum TNF-α and IL-17 levels in OLP patients.
Conclusion
Cx43 mRNA and protein levels in salivary EVs serve as effective biomarkers for diagnosing OLP and are significantly associated with disease activity and inflammatory markers. This makes Cx43 a promising candidate for non-invasive diagnosis of OLP.
期刊介绍:
Archives of Oral Biology is an international journal which aims to publish papers of the highest scientific quality in the oral and craniofacial sciences. The journal is particularly interested in research which advances knowledge in the mechanisms of craniofacial development and disease, including:
Cell and molecular biology
Molecular genetics
Immunology
Pathogenesis
Cellular microbiology
Embryology
Syndromology
Forensic dentistry