A Molecular Hypothesis on Malignant Transformation of Oral Lichen Planus: A Systematic Review and Meta-Analysis of Cancer Hallmarks Expression in This Oral Potentially Malignant Disorder
Metadatos
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MDPI
Materia
oral lichen planus oral cancer hallmarks of cancer
Fecha
2024-07-23Referencia bibliográfica
Keim del Pino, C. & Ramos García, P. & González Moles, M.A. Cancers 2024, 16, 2614. [https://doi.org/10.3390/cancers16152614]
Resumen
We aimed to qualitatively and quantitatively analyze, through a systematic review and
meta-analysis, the current evidence on the differential expression of the hallmarks of cancer in oral
lichen planus (OLP) samples, in order to know the earliest molecular mechanisms that could be
involved in the malignant transformation of this oral potentially malignant disorder. We searched
MEDLINE/PubMed, Embase,Web of Science, and Scopus for studies published before November
2023. We evaluated the methodological quality of studies and carried out meta-analyses to fulfill
our objectives. Inclusion criteria were met by 110 primary-level studies, with 7065 OLP samples,
in which the expression of 104 biomarkers were analyzed through immunohistochemistry. Most
OLP samples showed sustained cell proliferation signaling (65.48%, 95%CI = 51.87–78.02), antiapoptotic
pathways (55.93%, 95%CI = 35.99–75.0), genome instability (48.44%, 95%CI = 13.54–84.19),
and tumor-promoting inflammation events (83.10%, 95%CI = 73.93–90.74). Concurrently, OLP
samples also harbored tumor growth suppressor mechanisms (64.00%, 95%CI = 53.27–74.12). In
conclusion, current evidence indicates that molecular mechanisms promoting hyperproliferative
signaling, an antiapoptotic state with genomic instability, and an escape of epithelial cells from
immune destruction, are developed in LP-affected oral mucosa. It is plausible that these events
are due to the actions exerted by the chronic inflammatory infiltrate. Malignant transformation
appears to be prevented by tumor suppressor genes, which showed consistent upregulation in
OLP samples.