Adeno-associated virus-mediated delivery of a mutant endostatin suppresses ovarian carcinoma growth in mice

I. V. Subramanian; R. Ghebre; S. Ramakrishnan

doi:10.1038/sj.gt.3302352

Adeno-associated virus-mediated delivery of a mutant endostatin suppresses ovarian carcinoma growth in mice

I. V. Subramanian, R. Ghebre, S. Ramakrishnan

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39 Scopus citations

Abstract

Earlier studies have shown that a point mutation in human endostatin at position 125 (human endostatin wherein proline 125 was substituted with alanine, P125A-endostatin) improves endothelial cell binding and antiangiogenic activity. In the present study, we investigated the effect of recombinant adeno-associated virus (rAAV)-mediated gene delivery of P125A-endostatin (rAAV-P125Aendo) in a mouse model of ovarian carcinoma. Intramuscular (i.m.) injection of rAAV-P125Aendo resulted in a dose-dependent increase in serum endostatin levels. Consequently, vascular endothelial growth factor- and basic fibroblast growth factor-mediated angiogenesis was significantly inhibited in mice injected with rAAV-P125Aendo as compared to control mice injected with rAAV-LacZ. Furthermore, gene therapy using rAAV-P125Aendo construct showed sustained secretion of P125A-endostatin for up to 9 weeks after a single i.m. administration. Recombinant AAV-P125Aendo injection significantly inhibited the growth of human ovarian cancer cells in athymic nude mice. Immunofluorescence studies of residual tumors surgically removed from the rAAV-P125Aendo-treated animals showed decreased number of vessel ends and vessel length, indicating inhibition of angiogenesis. These studies suggest that recombinant AAV-mediated antiangiogenic gene therapy methods can be used to inhibit ovarian cancer growth.

Original language	English (US)
Pages (from-to)	30-38
Number of pages	9
Journal	Gene therapy
Volume	12
Issue number	1
DOIs	https://doi.org/10.1038/sj.gt.3302352
State	Published - Jan 2005

Bibliographical note

Funding Information:
We thank Dr C Le and RL Bliss (Biostatistics Core, University of Minnesota Cancer Center) for statistical analysis. We also thank Dr Y Yokoyama for helpful suggestions. This work was supported in part by grants from the Minnesota Ovarian Cancer Alliance, Sparboe and Women’s Health Fund Endowment and DAM 17-99-1-9564 from the USARMY.

Keywords

Angiogenesis
Endostatin
Mouse model
Ovarian cancer
rAAV

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This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1038/sj.gt.3302352

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abstract = "Earlier studies have shown that a point mutation in human endostatin at position 125 (human endostatin wherein proline 125 was substituted with alanine, P125A-endostatin) improves endothelial cell binding and antiangiogenic activity. In the present study, we investigated the effect of recombinant adeno-associated virus (rAAV)-mediated gene delivery of P125A-endostatin (rAAV-P125Aendo) in a mouse model of ovarian carcinoma. Intramuscular (i.m.) injection of rAAV-P125Aendo resulted in a dose-dependent increase in serum endostatin levels. Consequently, vascular endothelial growth factor- and basic fibroblast growth factor-mediated angiogenesis was significantly inhibited in mice injected with rAAV-P125Aendo as compared to control mice injected with rAAV-LacZ. Furthermore, gene therapy using rAAV-P125Aendo construct showed sustained secretion of P125A-endostatin for up to 9 weeks after a single i.m. administration. Recombinant AAV-P125Aendo injection significantly inhibited the growth of human ovarian cancer cells in athymic nude mice. Immunofluorescence studies of residual tumors surgically removed from the rAAV-P125Aendo-treated animals showed decreased number of vessel ends and vessel length, indicating inhibition of angiogenesis. These studies suggest that recombinant AAV-mediated antiangiogenic gene therapy methods can be used to inhibit ovarian cancer growth.",

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note = "Funding Information: We thank Dr C Le and RL Bliss (Biostatistics Core, University of Minnesota Cancer Center) for statistical analysis. We also thank Dr Y Yokoyama for helpful suggestions. This work was supported in part by grants from the Minnesota Ovarian Cancer Alliance, Sparboe and Women{\textquoteright}s Health Fund Endowment and DAM 17-99-1-9564 from the USARMY.",

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N1 - Funding Information: We thank Dr C Le and RL Bliss (Biostatistics Core, University of Minnesota Cancer Center) for statistical analysis. We also thank Dr Y Yokoyama for helpful suggestions. This work was supported in part by grants from the Minnesota Ovarian Cancer Alliance, Sparboe and Women’s Health Fund Endowment and DAM 17-99-1-9564 from the USARMY.

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N2 - Earlier studies have shown that a point mutation in human endostatin at position 125 (human endostatin wherein proline 125 was substituted with alanine, P125A-endostatin) improves endothelial cell binding and antiangiogenic activity. In the present study, we investigated the effect of recombinant adeno-associated virus (rAAV)-mediated gene delivery of P125A-endostatin (rAAV-P125Aendo) in a mouse model of ovarian carcinoma. Intramuscular (i.m.) injection of rAAV-P125Aendo resulted in a dose-dependent increase in serum endostatin levels. Consequently, vascular endothelial growth factor- and basic fibroblast growth factor-mediated angiogenesis was significantly inhibited in mice injected with rAAV-P125Aendo as compared to control mice injected with rAAV-LacZ. Furthermore, gene therapy using rAAV-P125Aendo construct showed sustained secretion of P125A-endostatin for up to 9 weeks after a single i.m. administration. Recombinant AAV-P125Aendo injection significantly inhibited the growth of human ovarian cancer cells in athymic nude mice. Immunofluorescence studies of residual tumors surgically removed from the rAAV-P125Aendo-treated animals showed decreased number of vessel ends and vessel length, indicating inhibition of angiogenesis. These studies suggest that recombinant AAV-mediated antiangiogenic gene therapy methods can be used to inhibit ovarian cancer growth.

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Adeno-associated virus-mediated delivery of a mutant endostatin suppresses ovarian carcinoma growth in mice

Abstract

Bibliographical note

Keywords

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