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Malignant transformation of oral lichen planus and related genetic factors KCI 등재후보

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  • URLhttps://db.koreascholar.com/Article/Detail/388633
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대한구강생물학회 (The Korean Academy of Oral Biology)
초록

Oral lichen planus (OLP) is a chronic inflammatory disease observed in approximately 0.5–2.2% of the population, and it is recognized as a premalignant lesion that can progress into oral squamous cell carcinoma (OSCC). The rate of malignant transformation is approximately 1.09–2.3%, and the risk factors for malignant transformation are age, female, erosive type, and tongue site location. Malignant transformation of OLP is likely related to the low frequency of apoptotic phenomena. Therefore, apoptosis-related genetic factors, like p53, BCL-2, and BAX are reviewed. Increased p53 expression and altered expression of BCL-2 and BAX were observed in OLP patients, and the malignant transformation rate in these patients was relatively higher. The involvement of microRNA (miRNA) in the malignant transformation of OLP is also reviewed. Because autophagy is involved in cell survival and death through the regulation of various cellular processes, autophagy-related genetic factors may function as factors for malignant transformation. In OLP, decreased levels of ATG9B mRNA and a higher expression of IGF1 were observed, suggesting a reduction in cell death and autophagic response. Activated IGF1-PI3K/AKT/mTor cascade may play an important role in a signaling pathway related to the malignant transformation of OLP to OSCC. Recent research has shown that miRNAs, such as miR-199 and miR-122, activate the cascade, increasing the prosurvival and proproliferative signals.

목차
Introduction
Malignant Transformation to OralSquamous Cell Carcinoma
Genetic Factors Related to Oral LichenPlanus
    1. Apoptosis related genetic factors
    2. Autophagy related genetic factors
References
저자
  • Eurim C. Hwang(Department of Oral Physiology, School of Dentistry, Seoul National University)
  • Se-Young Choi(Department of Oral Physiology, School of Dentistry, Seoul National University)
  • Jeong Hee Kim(Department of Oral Biochemistry and Molecular Biology, College of Dentistry, Kyung Hee University/Department of KHU-KIST Converging Science and Technology, Graduate School, Kyung Hee University) Correspondence to