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Qualitative expression of hypoxia-inducible factor-1α in malignant transformation of oral submucous fibrosis: An immunohistochemical study

BACKGROUND: Oral submucous fibrosis (OSF) is a precancerous condition predominantly seen in people of Asian descent. About 7%–12% of OSF patients develop oral squamous cell carcinoma. Morphological features of OSF, especially fibrosis, suggest a possibility of hypoxic environment in diseased tissues...

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Detalles Bibliográficos
Autores principales: Pereira, Treville, Surve, Ridima, Shetty, Subraj, Gotmare, Swati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269283/
https://www.ncbi.nlm.nih.gov/pubmed/32508457
http://dx.doi.org/10.4103/jomfp.JOMFP_234_19
Descripción
Sumario:BACKGROUND: Oral submucous fibrosis (OSF) is a precancerous condition predominantly seen in people of Asian descent. About 7%–12% of OSF patients develop oral squamous cell carcinoma. Morphological features of OSF, especially fibrosis, suggest a possibility of hypoxic environment in diseased tissues. Neovascularization and increased glycolysis, represent adaptations to a hypoxic microenvironment that are correlated with tumor invasion and metastasis. The adaptation of cells to hypoxia appears to be mediated through hypoxia-inducible factor-1α (HIF-1α). HIF-1α is said to be associated with malignant transformation of epithelium in other sites. AIM: The aim of this study was to investigate the relationship between the expression of HIF-1α in OSMF and its role in malignant transformation. MATERIALS AND METHODS: A retrospective study which included 20 histopathologically diagnosed cases of OSF was conducted. A qualitative evaluation of HIF-1α was performed. Statistical analysis was carried out using the IBM Statistical Package for Social Sciences 20.0 version (IBM Corporation, Armonk, NY, USA). RESULTS: Results showed an increased expression of HIF-1α in OSF. CONCLUSION: HIF-1α appears to play a role in malignant transformation of OSF.