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Targeting CD99 in association with doxorubicin: an effective combined treatment for Ewing's sarcoma.
Scotlandi, Katia; Perdichizzi, Stefania; Bernard, Ghislaine; Nicoletti, Giordano; Nanni, Patrizia; Lollini, Pier-Luigi; Curti, Antonio; Manara, Maria Cristina; Benini, Stefania; Bernard, Alain; Picci, Piero.
Afiliação
  • Scotlandi K; Laboratorio di Ricerca Oncologica, Istituti Ortopedici Rizzoli, Bologna 40136, Italy. katia.scotlandi@ior.it
Eur J Cancer ; 42(1): 91-6, 2006 Jan.
Article em En | MEDLINE | ID: mdl-16326096
ABSTRACT
CD99 is a 32kDa surface glycoprotein that is involved in the migration of leukocytes, cell-cell adhesion and apoptosis of T cells and Ewing's sarcoma (ES) cells, two cell types with a high level of CD99 expression. Engagement of the molecule induces a rapid death signal that appears to be related to the level of expression of this antigen. The rapid apoptosis induced by agonistic anti-CD99 monoclonal antibodies is of clinical interest in ES, a tumour for which no new drugs have been described as clearly effective in the last 10 years. In this study, we show that an anti-CD99 monoclonal antibody can be used to advantage in association with doxorubicin. Striking effectiveness was observed against local tumours and metastases. No remarkably toxic effects of anti-CD99 monoclonal antibody were found in bone marrow against blood precursors. These results provide the necessary rationale and support for a novel modality of therapeutic intervention, which may have application in the care of patients with ES.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma de Ewing / Doxorrubicina / Moléculas de Adesão Celular / Antibióticos Antineoplásicos / Anticorpos Monoclonais Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2006 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma de Ewing / Doxorrubicina / Moléculas de Adesão Celular / Antibióticos Antineoplásicos / Anticorpos Monoclonais Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2006 Tipo de documento: Article