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Updated: Oct 8, 2025

Comprehensive DNA Methylation Analysis Using a Methyl-CpG-binding Domain Capture-based Method in Chronic Lymphocytic Leukemia Patients
Published on: June 16, 2017
Is OLP potentially malignant? A clue from ZNF582 methylation
Yu-Wei Chiu1,2,3, Yee-Fun Su4, Cheng-Chieh Yang3,5
1Department of Stomatology, Chung Shan Medical University Hospital, Taichung, Taiwan.
Oral lichen planus (OLP) is unlikely to be potentially malignant, as ZNF582 methylation (ZNF582m) levels are lower in OLP lesions than in dysplasia or OSCC. ZNF582m may help distinguish OLP from malignant conditions.
Area of Science:
- Oral pathology
- Molecular oncology
- Cancer biomarkers
Background:
- The potential for oral lichen planus (OLP) to undergo malignant transformation remains a subject of debate.
- Understanding molecular markers associated with OLP and its progression to oral squamous cell carcinoma (OSCC) is crucial for accurate diagnosis and prognosis.
Purpose of the Study:
- To investigate the association of ZNF582 methylation (ZNF582m) levels with OLP lesions.
- To differentiate ZNF582m patterns in OLP, oral dysplasia, and OSCC.
- To assess ZNF582m as a potential biomarker for malignant transformation.
Main Methods:
- A case-control study was conducted involving patients with OLP, dysplasia, OSCC, and healthy controls.
- ZNF582m levels were quantified in lesion and adjacent normal mucosal tissues.
- High-risk habits (betel nut chewing, smoking) were analyzed in relation to ZNF582m.
Main Results:
- OLP lesions exhibited significantly lower ZNF582m compared to dysplasia and OSCC.
- ZNF582m in adjacent normal mucosa increased progressively from OLP to dysplasia to OSCC patients.
- ZNF582m in OLP patients was not influenced by high-risk habits, unlike in dysplasia/OSCC patients.
Conclusions:
- The findings suggest that OLP is unlikely to be a potentially malignant disorder based on ZNF582m levels.
- ZNF582m shows potential as a biomarker to differentiate OLP from dysplastic features and OSCC.
- ZNF582m may aid in monitoring malignant transformation in oral potentially malignant disorders.
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