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Immunohistochemical analysis of SHH, SMO and GLI-1 proteins in epithelial odontogenic lesions.

Abstract
The present study analyzed the expression of proteins involved in the sonic hedgehog signaling pathway (SHH, SMO, and GLI-1) in benign epithelial odontogenic lesions (odontogenic keratocyst - OKC, ameloblastoma - AB, and adenomatoid odontogenic tumor - AOT) in order to identify the role of these proteins in the pathogenesis of these lesions. The sample consisted of 20 OKCs, 20 ABs, and 10 AOTs. The Kruskal-Wallis, Mann-Whitney U, and Spearman's (r) tests were used for statistical analysis, with the level of significance set at 5% (p < 0.05). The membrane/cytoplasmic expression of SHH was significantly higher in AB compared to AOT (p = 0.022) and OKC (p = 0.02). No differences were found in the membrane/cytoplasmic expression of SMO between the lesions studied. Regarding GLI-1, significant differences were observed at the nuclear level for AB and OKC compared to AOT (p < 0.0001). In addition, significant positive correlations were found between cytoplasmic and nuclear GLI-1 in AB (r = 0.482; p = 0.031) and OKC (r = 0.865; p < 0.0001), and between membrane/cytoplasmic SMO and cytoplasmic GLI-1 in AOT (r = 0.667; p = 0.035) and OKC (r = 0.535; p = 0.015). The results of this study confirm the participation of the sonic hedgehog signaling pathway in the pathogenesis of the lesions studied. Overexpression of SHH in ABs and nuclear expression of GLI-1 in ABs and OKCs indicate that these proteins contribute to the more aggressive behavior of these two lesions when compared to AOT.
AuthorsKatianne Soares Rodrigues, Hellen Bandeira de Pontes Santos, Everton Freitas de Morais, Roseana de Almeida Freitas
JournalBrazilian dental journal (Braz Dent J) 2022 Sep-Oct Vol. 33 Issue 5 Pg. 91-99 ISSN: 1806-4760 [Electronic] Brazil
PMID36287504 (Publication Type: Journal Article)
Chemical References
  • Hedgehog Proteins
  • SHH protein, human
  • SMO protein, human
  • Smoothened Receptor
  • GLI1 protein, human
Topics
  • Humans
  • Ameloblastoma (metabolism, pathology)
  • Hedgehog Proteins (metabolism)
  • Odontogenic Cysts (metabolism, pathology)
  • Odontogenic Tumors
  • Signal Transduction
  • Smoothened Receptor

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