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Expression of extracellular matrix proteins in ameloblastomas and adenomatoid odontogenic tumors.

Abstract
This study evaluated the expression of fibronectin, tenascin and type I collagen in ameloblastomas and adenomatoid odontogenic tumors (AOTs) aiming to contribute with the comprehension of the differences in the biological behavior of these tumors. Immunohistochemical technique was performed in 20 cases of ameloblastoma (16 solid and 4 desmoplastic) and in 10 cases of AOT. All tumors presented moderate fibronectin expression in the stroma. Solid ameloblastomas showed intense expression of fibronectin at the epithelial-mesenchymal interface, whereas desmoplastic ameloblastomas revealed no immunoexpression of fibronectin at this site. Ameloblastomas presented stronger immunoreactivity to tenascin than AOTs, especially at the epithelial-mesenchymal interface. AOTs and desmoplastic ameloblastomas showed intense labeling for type I collagen. The patterns of expression of the proteins studied agree with the locally more invasive behavior of ameloblastomas in comparison to AOTs. Our results might suggest a less invasive behavior of desmoplastic ameloblastoma in comparison to solid ameloblastoma.
AuthorsAna Miryam Costa de Medeiros, Cassiano Francisco Weege Nonaka, Hébel Cavalcanti Galvão, Lélia Batista de Souza, Roseana de Almeida Freitas
JournalEuropean archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery (Eur Arch Otorhinolaryngol) Vol. 267 Issue 2 Pg. 303-10 (Feb 2010) ISSN: 1434-4726 [Electronic] Germany
PMID19466441 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Biomarkers, Tumor
  • Collagen Type I
  • Extracellular Matrix Proteins
  • Fibronectins
  • Tenascin
Topics
  • Adenomatoid Tumor (metabolism, pathology)
  • Ameloblastoma (metabolism, pathology)
  • Biomarkers, Tumor (biosynthesis)
  • Collagen Type I (biosynthesis)
  • Extracellular Matrix Proteins (biosynthesis)
  • Fibronectins (biosynthesis)
  • Humans
  • Immunohistochemistry
  • Jaw Neoplasms (metabolism, pathology)
  • Odontogenic Tumors (metabolism, pathology)
  • Prognosis
  • Tenascin (biosynthesis)

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