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Anti-tumor effect of endostatin mediated by retroviral gene transfer in mice bearing renal cell carcinoma

Coutinho, Enia Lúcia ; de Sousa Andrade, Luciana Nogueira ; Chammas, Roger ; Morganti, Ligia ; Schor, Nestor ; Bellini, Maria Helena

The FASEB journal, 2007-10, Vol.21 (12), p.3153-3161 [Periódico revisado por pares]

United States: The Federation of American Societies for Experimental Biology

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Título:
Anti-tumor effect of endostatin mediated by retroviral gene transfer in mice bearing renal cell carcinoma
Autor: Coutinho, Enia Lúcia ; de Sousa Andrade, Luciana Nogueira ; Chammas, Roger ; Morganti, Ligia ; Schor, Nestor ; Bellini, Maria Helena
Assuntos: Angiogenesis Inhibitors - metabolism ; Animals ; antiangiogen‐esis ; Antineoplastic Agents - metabolism ; Apoptosis - physiology ; bioassay ; cancer ; Carcinoma, Renal Cell - metabolism ; Carcinoma, Renal Cell - pathology ; Carcinoma, Renal Cell - therapy ; Cell Line, Tumor ; Endostatins - genetics ; Endostatins - metabolism ; gene therapy ; Gene Transfer Techniques ; Humans ; Male ; Mice ; Mice, SCID ; Neoplasm Transplantation ; NIH 3T3 Cells ; Retroviridae - genetics ; Retroviridae - metabolism ; Transduction, Genetic ; Transplantation, Heterologous
É parte de: The FASEB journal, 2007-10, Vol.21 (12), p.3153-3161
Notas: http://www.fasebj.org/
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Descrição: We investigated whether transfer of the gene encoding the angiogenesis inhibitor endostatin into the NIH/3T3 fibroblast cell line could inhibit renal tumor growth in vivo. NIH/3T3 cells were transduced with retroviral vectors containing the murine endostatin (ES) gene. SCID mice bearing CaKi-1 derived tumors were given a subcutaneous injection of either ES-transduced cells or control cells and were monitored for tumor growth. At the end of the in vivo experiment, the mean tumor volume of treated mice was 51.6 ± 2.4 mm³, while the tumor volume of control was 234.5 ± 14.8 mm³. Microvascular density was significantly decreased on treatment (control 9.79 vs. ES 2.53%, <0.001) accompanied by a 23-fold increase in intraturmoral necrotic area and a 2.94-fold increase in the apoptotic index, determined by immunohistochemistry with anti- activated caspase-3. Apoptotic cells were found in foci enriched in infiltrating leukocytes. In conclusion, retroviral endostatin gene transfer led to secretion of functional endostatin that was sufficiently active to inhibit tumor angiogenesis and tumor growth. A second mechanism may also be implied in endostatin-dependent tumor regression, associated with tumor infiltration of leukocytes. Besides its antiangiogenic properties, endostatin may be a promising adjuvant to immunotherapy.--Coutinho, E. L., Nogueira de Sousa Andrade, L., Chammas, R., Morganti, L., Schor, N., Bellini, M. H. Anti-tumor effect of endostatin mediated by retroviral gene transfer in mice bearing renal cell carcinoma.
Editor: United States: The Federation of American Societies for Experimental Biology
Idioma: Inglês

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Anti-tumor effect of endostatin mediated by retroviral gene transfer in mice bearing renal cell carcinoma

Coutinho, Enia Lúcia ; de Sousa Andrade, Luciana Nogueira ; Chammas, Roger ; Morganti, Ligia ; Schor, Nestor ; Bellini, Maria Helena

United States: The Federation of American Societies for Experimental Biology

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