Downregulation of TNF-α and VEGF expression by Sp1 decoy oligodeoxynucleotides in mouse melanoma tumor

Autor(es)

Novak‚ E.M. ; Metzger‚ M. ; Chammas‚ R. ; Da Costa‚ M. ; Dantas‚ K. ; Manabe‚ C. ; Pires‚ J. ; De Oliveira‚ AC ; Bydlowski‚ SP

• Tipo de documento: Artigo Científico
• Fonte: Gene Therapy; v. 10, n. 23, p. 1992-1997, 2003.

Resumo

Melanoma tumor growth and progression are highly dependent on adequate blood supply through angiogenesis. Since several genes involved in angiogenesis revealed potential binding sites for the transcription factor Sp1, we have examined the effects of local inoculation of Sp1 decoy oligodeoxynucleotides (ODNs) on the growth of transplanted murine melanoma tumors and the expression of VEGF and TNF-alpha within these tumors. Treatment with Sp1 decoy ODNs, but not their mutated form, led to a significant increase ( P = 0.041) of the tumor necrotic area, as evaluated morphometrically. Tumor necrosis was associated with a significant decrease of microvascular density ( P = 0.012) and relative vascular area ( P = 0.026), as determined by counting CD34-positive vascular structures within the tumor microenvironment of Sp1 decoy ODNs and control ODN-treated tumors. RT-PCR experiments showed a strong decrease in the levels of VEGF(188) and VEGF(164) isoforms and a moderate decrease of TNF-alpha in Sp1 decoy-treated tumors. Taken together, our results indicate that Sp1 decoy ODNs may inhibit angiogenesis by affecting the gene expression of key players in angiogenesis such as TNF-alpha and VEGF. These findings indicate that Sp1 decoy ODNs may be a potential new therapeutic tool in antiangiogenic therapy. (AU)

• Processo FAPESP: 00/05381-2 - Estudo molecular do controle da expressão do fator de crescimento vascular endotelial (VEGF) em melanomas desenvolvidos em camundongos C57B16/J
• Beneficiário: Estela Maria Novak
• Modalidade de apoio: Auxílio à Pesquisa - Regular
• Processo FAPESP: 97/13100-9 - Dissialogangliosídios em melanomas
• Beneficiário: Roger Chammas
• Modalidade de apoio: Auxílio à Pesquisa - Regular
• Processo FAPESP: 99/00322-9 - Estudo integrado das alterações da fibra cardíaca, matriz extracelular, microcirculação e sistema nervoso autônomo, no desenvolvimento da remodelação cardiovascular
• Beneficiário: Maria de Lourdes Higuchi
• Modalidade de apoio: Auxílio à Pesquisa - Temático
• Processo FAPESP: 98/14247-6 - Center for Research on Cell-Based Therapy
• Beneficiário: Marco Antonio Zago
• Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs
• Processo FAPESP: 00/09011-5 - Utilização de emulsão lipídica como vetor de oligonucleotídeos antissenso para possível reversão do fenótipo de resistência a múltiplas drogas em células tumorais in vitro
• Beneficiário: Sergio Paulo Bydlowski
• Modalidade de apoio: Auxílio à Pesquisa - Regular