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TIMP-1 secreted by fibroblasts inhibits tumor cell invasion and metastasis in mouse melanoma / 生物医学工程学杂志
Journal of Biomedical Engineering ; (6): 610-614, 2009.
Article in Chinese | WPRIM | ID: wpr-294607
ABSTRACT
We constructed a recombinant adenoviral vector expressing human tissue inhibitors of metalloproteinase-1(TIMP-1), and evaluated the inhibition of TIMP-1 secreted by primary fibroblasts after infection with adenovirus-mediated TIMP-1 gene (Ad-TIMP-1) on tumor cell invasion and metastasis in mouse melanoma. It was found that TIMP-1 was detected in the supernatants of cultured mouse primary fibroblasts after infection with Ad-TIMP-1 by indirect enzyme-linked immunosorbent assay (ELISA). The TIMP-1 secreted by Ad-TIMP-1 infected primary fibroblast significantly inhibited B16BL6 cell invasion and metastasis both in vitro and in vivo. We also demonstrated that the primary fibroblasts transfected by Ad-TIMP-1, after being subcutaneously injected into mouse, can secreted TIMP-1 into the blood of mouse and maintained at the therapeutic in vivo levels of TIMP-1. These results suggest that the preparation of Ad-TIMP-1 infected primary fibroblast be an effective method to deliver TIMP-1 gene in vivo, which provides a new strategy of gene therapy and has the potential for clinical applications in the treatment of tumor cell metastasis.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / Therapeutics / Melanoma, Experimental / Recombinant Proteins / Genetic Therapy / Adenoviridae / Tissue Inhibitor of Metalloproteinase-1 / Fibroblasts / Genetics Limits: Animals / Female / Humans Language: Chinese Journal: Journal of Biomedical Engineering Year: 2009 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Pharmacology / Therapeutics / Melanoma, Experimental / Recombinant Proteins / Genetic Therapy / Adenoviridae / Tissue Inhibitor of Metalloproteinase-1 / Fibroblasts / Genetics Limits: Animals / Female / Humans Language: Chinese Journal: Journal of Biomedical Engineering Year: 2009 Type: Article