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Published on: June 15, 2016
MicroRNAs in oral lichen planus and potential miRNA-mRNA pathogenesis with essential cytokines: a review
Hui Ma1, Yuanqin Wu1, Huamei Yang1
1State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Abstract:
Oral lichen planus (OLP) is a potentially premalignant condition with unknown pathogenesis. Immune and inflammatory factors are thought to play important roles in the development of OLP, and cytokines, such as interferon (IFN)-γ and tumor necrosis factor (TNF)-α, can act as critical players in the immunopathogenesis of OLP. MicroRNAs (miRNAs) are closely correlated with cytokines in various inflammation-related diseases. In patients with OLP, miRNA-146a and miRNA-155 are increased in peripheral blood mononuclear cells, and numerous miRNAs have been shown to exhibit altered expression profiles in lesions. Although the microRNA-messenger RNA (miRNA-mRNA) network is thought to be involved in the development of OLP, in-depth studies are lacking. Here, we summarize current data on the mechanisms of action of miRNAs regulating typical cytokines in OLP, including interleukin (IL)-10, IL-17, IL-22, IFN-γ, and TNF-α, to study the genetic basis of the pathogenesis of OLP and to provide prospects of therapy.
Insights
Oral lichen planus (OLP), a premalignant condition, involves immune factors and cytokines. MicroRNAs (miRNAs) regulate these cytokines, offering potential therapeutic targets for OLP.
Area of Science:
- Immunology
- Molecular Biology
- Oral Pathology
Background:
- Oral lichen planus (OLP) is a potentially premalignant condition with largely unknown pathogenesis.
- Immune and inflammatory factors, particularly cytokines like interferon (IFN)-γ and tumor necrosis factor (TNF)-α, are implicated in OLP development.
- MicroRNAs (miRNAs) are increasingly recognized for their role in inflammation and disease, with altered miRNA expression observed in OLP lesions.
Purpose of the Study:
- To summarize current data on miRNA mechanisms regulating key cytokines in OLP.
- To elucidate the role of the microRNA-messenger RNA (miRNA-mRNA) network in OLP pathogenesis.
- To explore the genetic basis of OLP and identify potential therapeutic strategies.
Main Methods:
- Literature review and data summarization.
- Analysis of miRNA expression profiles in OLP patients.
- Investigation of miRNA-cytokine interactions in inflammation.
Main Results:
- Specific miRNAs (e.g., miRNA-146a, miRNA-155) are upregulated in OLP patients' cells.
- Altered expression of numerous miRNAs is detected in OLP lesions.
- miRNAs are shown to regulate critical cytokines involved in OLP, including IL-10, IL-17, IL-22, IFN-γ, and TNF-α.
Conclusions:
- The miRNA-mRNA network plays a significant role in OLP pathogenesis.
- Understanding miRNA-cytokine interactions provides insights into OLP's genetic basis.
- Targeting miRNAs offers promising therapeutic avenues for OLP.
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