Matrix metalloproteinases, TIMPs and growth factors regulating ameloblastoma behaviour


Autoria(s): SIQUEIRA, Adriane S.; CARVALHO, Marcia R. D.; MONTEIRO, Ana C. D.; FREITAS, Vanessa M.; JAEGER, Ruy G.; PINHEIRO, Joao J. V.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Aims: Ameloblastoma is an odontogenic neoplasm with local invasiveness and recurrence. We have previously suggested that growth factors and matrix metalloproteinases (MMPs) influence ameloblastoma invasiveness(1). The aim was to study expression of MMPs, tissue inhibitor of metalloproteinases (TIMPs) and growth factors in ameloblastoma. Methods and results: Thirteen cases of solid/multicystic ameloblastoma were examined. As a control, calcifying cystic odontogenic tumour (CCOT), a non-invasive odontogenic neoplasm with ameloblastomatous epithelium was also studied. Immunohistochemistry detected MMPs, TIMPs and growth factors in ameloblastoma and CCOT. The labelling index (LI) of MMP-9 and TIMP-2 was significantly higher in ameloblastoma compared with CCOT. The LI of epidermal growth factor (EGF), transforming growth factor (TGF)-alpha and epidermal growth factor receptor (EGFR) was also increased in ameloblastoma. This neoplasm showed greater expression of MMPs, TIMPs and growth factors compared with CCOT. We then analysed these molecules in ameloblastoma cells and stroma. Ameloblastoma cells exhibited increased LI of MMP-1, -2 and EGFR. We found a positive correlation between EGF and TIMP-1, and between TGF-alpha and TIMP-2. It is known that signals generated by growth factors are transduced by the ERK pathway. Ameloblastoma stroma exhibited the phosphorylated (activated) form of ERK. Conclusions: These results suggest an interplay involving growth factors MMPs and TIMPs that may contribute to ameloblastoma behaviour. Signals generated by this molecular network would be transduced by ERK 1/2 pathway.

The State of Sao Paulo Research Foundation (FAPESP)[2006/57079-4]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

The State of Sao Paulo Research Foundation (FAPESP)[2007/51950-8]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

The State of Sao Paulo Research Foundation (FAPESP)[06/54963-0]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Brazilian National Council for Scientific and Technological Development (CNPq)[471751/2003-0]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Brazilian National Council for Scientific and Technological Development (CNPq)[304868/2006-0]

Brazilian National Council for Scientific and Technological Development (CNPq)[470622/2007-5]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Brazilian National Council for Scientific and Technological Development (CNPq)[504667/2008-4]

Identificador

HISTOPATHOLOGY, v.57, n.1, p.128-137, 2010

0309-0167

http://producao.usp.br/handle/BDPI/28074

10.1111/j.1365-2559.2010.03596.x

http://dx.doi.org/10.1111/j.1365-2559.2010.03596.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

Relação

Histopathology

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #ameloblastoma #calcifying cystic odontogenic tumour #EGF #EGFR #ERK #growth factors #MMPs #odontogenic tumours #TGF-alpha #TIMPs #FACTOR RECEPTOR #IMMUNOHISTOCHEMICAL DETECTION #ODONTOGENIC-TUMORS #TISSUE INHIBITORS #TGF-ALPHA #EXPRESSION #CANCER #FAMILY #MMP #MICROENVIRONMENT #Cell Biology #Pathology
Tipo

article

original article

publishedVersion