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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.)

Endostatin neoadjuvant gene therapy extends survival in an orthotopic metastatic mouse model of renal cell carcinoma

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Autor(es):
Braga, Marina de Souza [1, 2] ; Chaves, Karen Barbosa [1] ; Chammas, Roger [3] ; Schor, Nestor [1] ; Bellini, Maria Helena [1, 2]
Número total de Autores: 5
Afiliação do(s) autor(es):
[1] Univ Fed Sao Paulo, Div Nephrol, Dept Med, Sao Paulo - Brazil
[2] Dept Biotechnol, IPEN CNEN, Sao Paulo - Brazil
[3] Univ Fed Sao Paulo, Dept Radiol, Sao Paulo - Brazil
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: BIOMEDICINE & PHARMACOTHERAPY; v. 66, n. 4, p. 237-241, JUN 2012.
Citações Web of Science: 6
Resumo

Despite recent advances in targeted therapy, renal cell carcinoma (RCC) remains one of the most lethal urologic malignancies. Approximately 30% of patients with localised RCC will develop metastases after curative surgery. Presurgical therapy has been explored for treatment of localised RCC. Endostatin (ES) is a fragment of collagen XVIII that possesses antiangiogenic activity. In this study, we examined the potential use of an antiangiogenic agent as a neoadjuvant therapy in an orthotopic metastatic mouse model of RCC. BALB/c mice bearing Renca cells were treated before nephrectomy with NIH/3T3-LendSN cells. At the end of the experiment, ES serum levels were measured. Primary and metastatic tumour area and microvascular area were determined. In the survival studies, mice were monitored daily until they died. ES serum levels in treated mice were higher in the control group (P < 0.05). The median primary tumour area and the mean microvascular area were significantly lower in the ES-treated group compared to control group (P < 0.05). The proliferation of Renca cells in the ES-treated group was significantly reduced compared with the control group (P < 0.01). ES therapy led to a significant reduction in the number of pulmonary metastatic nodules compared with the control group (P < 0.01). Kaplan-Meier survival curves showed that the probability of survival was significantly higher in mice receiving ES therapy (P = 0.0243, Log-Rank test). Our results indicated that neoadjuvant ES gene therapy has the potential to decrease tumour burden, extend survival, and may have clinical benefit in the management of RCC. (C) 2011 Elsevier Masson SAS. All rights reserved. (AU)

Processo FAPESP: 10/18969-0 - Estudo da regulação do NF-kB no carcinoma renal metastático após terapia gênica com endostatina
Beneficiário:Maria Helena Bellini Marumo
Modalidade de apoio: Auxílio à Pesquisa - Regular