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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Decreased expression of ADAMTS-1 in human breast tumors stimulates migration and invasion

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Autor(es):
Freitas, Vanessa M. [1] ; do Amaral, Jonatas Bussador [1] ; Silva, Thaiomara A. [1] ; Santos, Emerson S. [1, 2] ; Mangone, Flavia R. [3] ; Pinheiro, Joao de Jesus [1, 4] ; Jaeger, Ruy G. [1] ; Nagai, Maria A. [3] ; Machado-Santelli, Glaucia Maria [1]
Número total de Autores: 9
Afiliação do(s) autor(es):
[1] Univ Sao Paulo, Inst Ciencias Biomed, Dept Biol Celular & Desenvolvimento, BR-05508000 Sao Paulo - Brazil
[2] Univ Sao Paulo Ribeirao Preto, Fac Ciencias Farmaceut, Dept Anal Clin, BR-14040903 Ribeirao Preto, SP - Brazil
[3] Univ Sao Paulo, Fac Med, Dept Radiol & Oncol, Disciplina Oncol, BR-01246903 Sao Paulo - Brazil
[4] Fed Univ Para, Fac Odontol, Inst Ciencias Saude, Programa Posgrad Odontol, BR-66075110 Belem, Para - Brazil
Número total de Afiliações: 4
Tipo de documento: Artigo Científico
Fonte: Molecular Cancer; v. 12, JAN 5 2013.
Citações Web of Science: 25
Resumo

Background: ADAMTS-1 (a disintegrin and metalloprotease with thrombospondin motifs) is a member of the ADAMTS family of metalloproteases. Here, we investigated mRNA and protein levels of ADAMTS-1 in normal and neoplastic tissues using qPCR, immunohistochemistry and immunoblot analyses, and we addressed the role of ADAMTS-1 in regulating migration, invasion and invadopodia formation in breast tumor cell lines. Results: In a series of primary breast tumors, we observed variable levels of ADAMTS-1 mRNA expression but lower levels of ADAMTS-1 protein expression in human breast cancers as compared to normal tissue, with a striking decrease observed in high-malignancy cases (triple-negative for estrogen, progesterone and Her-2). This result prompted us to analyze the effect of ADAMTS-1 knockdown in breast cancer cells in vitro. MDA-MB-231 cells with depleted ADAMTS-1 expression demonstrated increased migration, invasion and invadopodia formation. The regulatory mechanisms underlying the effects of ADAMTS-1 may be related to VEGF, a growth factor involved in migration and invasion. MDA-MB-231 cells with depleted ADAMTS-1 showed increased VEGF concentrations in conditioned medium capable of inducing human endothelial cells (HUVEC) tubulogenesis. Furthermore, expression of the VEGF receptor (VEGFR2) was increased in MDA-MB-231 cells as compared to MCF7 cells. To further determine the relationship between ADAMTS-1 and VEGF regulating breast cancer cells, MDA-MB-231 cells with reduced expression of ADAMTS-1 were pretreated with a function-blocking antibody against VEGF and then tested in migration and invasion assays; both were partially rescued to control levels. Conclusions: ADAMTS-1 expression was decreased in human breast tumors, and ADAMTS-1 knockdown stimulated migration, invasion and invadopodia formation in breast cancer cells in vitro. Therefore, this series of experiments suggests that VEGF is involved in the effects mediated by ADAMTS-1 in breast cancer cells. (AU)

Processo FAPESP: 06/54963-0 - Estudo dos genes AAEF2 e ADAMTS-1 na migração e invasão de células tumorais de mama cultivadas em ambiente bidiomensional e tridimensional
Beneficiário:Vanessa Morais Freitas
Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
Processo FAPESP: 06/01026-0 - Análise funcional de genes potencialmente regulados pelo receptor de estrógeno e/ou pelo oncogene ERBB2: implicações no diagnóstico, prognóstico e tratamento do câncer de mama
Beneficiário:Maria Aparecida Nagai
Modalidade de apoio: Auxílio à Pesquisa - Temático
Processo FAPESP: 08/57103-8 - Dinamica de formacao de invadopodios em linhagens tumorais tratadas por peptideos bioativos da laminina. estudo por microscopia 4d
Beneficiário:Ruy Gastaldoni Jaeger
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 10/07699-1 - Protease ADAMTS-1 influenciando o comportamento e o microambiente do câncer de mama
Beneficiário:Vanessa Morais Freitas
Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores