Abstract
Endostatin is an important endogenous inhibitor of neovascularization, which has been widely used in anti-angiogenesis therapy for cancer. To fully explore the potential of endostatin, we evaluated the anti-tumor efficacy of the combination of recombinant human endostatin adenovirus and low-dose gemcitabine in nude mice. We injected recombinant human endostatin adenovirus intratumorally plus a low dose of gemcitabine i.p. routinely. The combination treatment produced no side-effects, and resulted in marked suppression in tumor formation and growth of established human lung carcinoma xenografts in nude mice, with decreased microvessel density and increased apoptosis percentage. Our data support the idea of synergistic anti-tumor properties of endostatin plus low-dose chemotherapy against human lung cancer in vivo.
MeSH terms
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Adenoviridae / genetics
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Animals
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Antineoplastic Agents / administration & dosage
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Antineoplastic Agents / therapeutic use*
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Cell Line, Tumor
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Deoxycytidine / administration & dosage
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Deoxycytidine / analogs & derivatives*
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Deoxycytidine / therapeutic use
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Drug Synergism
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Endostatins / administration & dosage
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Endostatins / genetics
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Endostatins / therapeutic use*
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Female
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Gemcitabine
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Genetic Therapy*
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Genetic Vectors
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Humans
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Injections, Intralesional
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Injections, Intraperitoneal
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Mice
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Mice, Nude
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Neoplasm Transplantation
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Neoplasms, Experimental / blood supply
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Neoplasms, Experimental / drug therapy*
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Neovascularization, Pathologic / prevention & control*
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Recombinant Proteins / administration & dosage
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Recombinant Proteins / therapeutic use
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Xenograft Model Antitumor Assays
Substances
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Antineoplastic Agents
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Endostatins
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Recombinant Proteins
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Deoxycytidine
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Gemcitabine