ArticleClinical oral investigations2025
Integrating genotype-phenotype correlations into the diagnostic workflow of odontogenic tumors and cysts: insights from a 69 lesion cohort.
Article in Clinical oral investigations, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Hybrid/collision ameloblastoma-ameloblastic fibroma: a case with molecular features supporting a tumor-in-tumor model.Virchows Archiv : an international journal of pathology · 2026Article
- Immunohistochemical Expression of CK13 and Molecular Analysis of KRT13 and APC in Odontogenic Ghost Cell Lesions, Adenoid Ameloblastoma, and Conventional Ameloblastoma.Head and neck pathology · 2026Article
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4 authors.
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Abstract
objectivesOdontogenic tumors (OTs) represent a heterogeneous group of lesions ranging from hamartomatous or non-neoplastic proliferations to benign and malignant neoplasms with metastatic potential. Their classification remains challenging due to morphological and molecular variability. In this study, we performed comprehensive molecular profiling of odontogenic lesions—excluding previously analyzed ameloblastomas—to identify genomic alterations that define molecular subtypes and evaluate their diagnostic significance and potential therapeutic implications. MATERIALS AND
methodsA total of 88 odontogenic lesions were analyzed, including 25 cysts and 63 benign or malignant tumors, classified according to the 2022 5th edition of the World Health Organization (WHO) classification. Targeted next-generation sequencing (NGS) was performed to detect somatic mutations. Mutational patterns were correlated with histological subtypes and clinical parameters such as age, gender, lesion location, and recurrence.
resultsSomatic mutations were identified in 46 of 69 lesions successfully sequenced (66.7%). Among malignant tumors, genomic alterations—including gene fusions and mutations—were detected in 75% of cases. The highest mutation frequency was observed in OTs of epithelial origin. Notably, 11 of the 46 mutated cases harbored concurrent alterations in two genes.
conclusionsMolecular profiling serves as a valuable diagnostic adjunct in evaluating odontogenic tumors and cysts. Incorporating mutational analysis into routine workflows may enhance diagnostic precision, particularly in small or ambiguous biopsies, and may provide preliminary insights for future development of targeted therapeutic approaches. CLINICAL RELEVANCE: This study highlights the diagnostic value of integrating somatic mutation analysis into the standard evaluation of odontogenic lesions and highlights its potential adjunctive role in diagnostically challenging cases and as a basis for future therapeutic investigations.
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