TY - JOUR
T1 - The genomic and proteomic landscape in oral lichen planus versus oral squamous cell carcinoma
T2 - a scoping review
AU - Xie, Fangyi
AU - Meves, Alexander
AU - Lehman, Julia S.
N1 - Funding Information:
We would like to thank the following people for their contributions to this article: Leslie C. Hassett M.L.S, Outreach Librarian, for the literature search; Asha Nair Ph.D. M.S., Bioinformatics Core Supervisor, for visualization of data. This work was supported by the British Association of Dermatologists’ Geoffrey Dowling Fellowship and the Appignani Lichen Planus Benefactor Fund. The funding was not directly for this review, and the funders have not been involved in the review process. We express thanks to the anonymous reviewers for their suggestions in improving the manuscript.
Publisher Copyright:
© 2022 the International Society of Dermatology.
PY - 2022/10
Y1 - 2022/10
N2 - Background: Oral lichen planus (OLP), a World Health Organization (WHO)-classified oral potentially malignant condition, confers a 1% risk of transformation to oral squamous cell carcinoma (OSCC). There does not appear to be a consensus understanding of the underlying molecular events. This scoping review aimed to identify critical molecular pathways and highlight gaps in existing knowledge on malignant transformation in OLP. Methods: Following Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocols (PRISMA-P) guidelines, a comprehensive literature search and methodical screening identified 61 relevant studies detailing molecular differences between OLP and OSCC. Results: Molecular changes shared between OLP and OSCC included those affecting cellular proliferation (altered p53 expression, hypermethylation of p16/CDKN2A, MYC gains, increased ki-67), apoptosis (increased bcl-2 and survivin expression), extracellular matrix (ECM) remodeling (increased matrix metalloproteinase [MMP] expression), and transcriptional control (altered bmi1 and microRNA [miRNA] expression). In addition, some molecular alterations accumulated incrementally from control to OLP to OSCC or were present in higher-risk erosive variants of OLP or transformed OLP. Few studies included rigorous diagnostic inclusion criteria or unbiased discovery methods. Conclusions: Results of this review support the potentially malignant nature of OLP and imply that molecular events associated with malignant transformation may be heterogeneous. In addition, findings in this review highlight the need for additional studies using rigorous diagnostic inclusion criteria and unbiased discovery methods to further understand this process.
AB - Background: Oral lichen planus (OLP), a World Health Organization (WHO)-classified oral potentially malignant condition, confers a 1% risk of transformation to oral squamous cell carcinoma (OSCC). There does not appear to be a consensus understanding of the underlying molecular events. This scoping review aimed to identify critical molecular pathways and highlight gaps in existing knowledge on malignant transformation in OLP. Methods: Following Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocols (PRISMA-P) guidelines, a comprehensive literature search and methodical screening identified 61 relevant studies detailing molecular differences between OLP and OSCC. Results: Molecular changes shared between OLP and OSCC included those affecting cellular proliferation (altered p53 expression, hypermethylation of p16/CDKN2A, MYC gains, increased ki-67), apoptosis (increased bcl-2 and survivin expression), extracellular matrix (ECM) remodeling (increased matrix metalloproteinase [MMP] expression), and transcriptional control (altered bmi1 and microRNA [miRNA] expression). In addition, some molecular alterations accumulated incrementally from control to OLP to OSCC or were present in higher-risk erosive variants of OLP or transformed OLP. Few studies included rigorous diagnostic inclusion criteria or unbiased discovery methods. Conclusions: Results of this review support the potentially malignant nature of OLP and imply that molecular events associated with malignant transformation may be heterogeneous. In addition, findings in this review highlight the need for additional studies using rigorous diagnostic inclusion criteria and unbiased discovery methods to further understand this process.
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U2 - 10.1111/ijd.16273
DO - 10.1111/ijd.16273
M3 - Article
C2 - 35575880
AN - SCOPUS:85130136345
SN - 0011-9059
VL - 61
SP - 1227
EP - 1236
JO - International Journal of Dermatology
JF - International Journal of Dermatology
IS - 10
ER -