Abstract
Objective
The aim of this study is to assess whether C1772T and G1790A hypoxia-inducible factor-1 (HIF-1)α polymorphisms are associated with risk of oral lichen planus (OLP).
Material and methods
Restriction fragment length polymorphism analysis was used to investigate HIF-1α C1779T and G1790A polymorphisms in 32 OLP and 88 individuals without OLP.
Results
The frequency of the CC, TT, GA, and AA genotypes was higher in patients with OLP. Notably, individuals carrying the C and A, and T and A haplotypes showed a significant association OLP risk.
Conclusions
Our study demonstrated that the C1772T and G1790A polymorphisms of HIF-1α gene increased the risk of OLP. C1772T and G1790A polymorphisms of HIF-1α gene had differing patterns of allelic imbalance in the normal samples and subsequent chronic lesions. Further studies are necessary to elucidate the HIF-1α pathway in OLP, which would facilitate the development of novel therapeutic strategies for the prevention and treatment of OLP.
Clinical relevance
These results, in conjunction with previous studies, suggest that HIF-1α may play important roles in the chronicity of oral mucosa lesions of OLP patients. Taken together, we suggest that HIF-1α polymorphisms enhance its target genes, thereby altering the microenvironment and supporting sequential release of inflammatory mediators or cellular events in OLP. It appears unlikely that inhibition of a single proinflammatory mediator will prove useful in clinical practice, but several ways to reprogram mediators engaged in a wide array of roles simultaneously are encouraging.
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Acknowledgments
This study was supported by grants from the Conselho Nacional de Desenvolvimento Científico e Tecnológico and the Fundação de Amparo a Pesquisa do Estado de Minas Gerais. Dr Guimarães is a research fellow of CNPq. Dr De Paula is a research fellow of FAPEMIG.
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No conflicts declared.
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de Carvalho Fraga, C.A., Alves, L.R., Marques-Silva, L. et al. High HIF-1α expression genotypes in oral lichen planus. Clin Oral Invest 17, 2011–2015 (2013). https://doi.org/10.1007/s00784-013-0920-8
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DOI: https://doi.org/10.1007/s00784-013-0920-8