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Immunoexpression of MMP‐9, VEGF, and vWF in central and peripheral giant cell lesions of the jaws
Author(s) -
Matos Felipe R.,
aka Cassiano F. W.,
Miguel Márcia C. da C.,
Galvão Hébel C.,
Souza Lélia B. de,
Freitas Roseana de A.
Publication year - 2011
Publication title -
journal of oral pathology and medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.887
H-Index - 83
eISSN - 1600-0714
pISSN - 0904-2512
DOI - 10.1111/j.1600-0714.2010.00993.x
Subject(s) - pathology , matrix metalloproteinase , vascular endothelial growth factor , giant cell , lesion , medicine , pathological , von willebrand factor , angiogenesis , vegf receptors , cancer research , immunology , platelet
J Oral Pathol Med (2011) 40 : 338–344 Background: Central giant cell lesion (CGCL) and peripheral giant cell lesion (PGCL) are pathological conditions of the jaws that share the same microscopic features, but differ clinically in terms of their behavior. Our aim was to compare the immunoexpression of vascular endothelial growth factor (VEGF) and matrix metalloproteinase‐9 (MMP‐9) in CGCL and PGCL, relating them to the angiogenic index. Methods: Twenty CGCL and 20 PGCL were selected for analysis of the immunoexpression of MMP‐9 and VEGF in multinucleated giant cells (MGC) and mononucleated cells (MC). Angiogenic index was determined by microvessel count (MVC) using anti‐von Willebrand factor antibody. Results: The CGCL showed slightly higher expression of MMP‐9 than PGCL. In comparison with PGCL, the CGCL showed higher expression of VEGF both in MC ( P < 0.05) and in total cells ( P < 0.05). PGCL exhibited higher MVC than CGCL ( P < 0.05). Conclusions: MMP‐9 and VEGF might play an important role in the osteoclastogenesis process in CGCL. The higher MVC in PGCL might be related to the reactive nature of these lesions.