Development and characterization of a synthetic promoter for selective expression in proliferating endothelial cells
| Autor: | K. Anwer, Sean M. Sullivan, Paul Szymanski |
|---|---|
| Rok vydání: | 2006 |
| Předmět: |
Endothelium
Genetic enhancement Genetic Vectors Gene Expression Transplants Cell Cycle Proteins Biology Transfection Cell Line Mice In vivo Drug Discovery Genetics medicine Animals Humans Cytotoxic T cell Promoter Regions Genetic Enhancer Molecular Biology Genetics (clinical) Cell Proliferation Endothelins Endothelial Cells Nuclear Proteins Promoter Genetic Therapy Cell cycle Molecular biology Enhancer Elements Genetic medicine.anatomical_structure NIH 3T3 Cells Systemic administration Cancer research Molecular Medicine Cattle Female |
| Zdroj: | The Journal of Gene Medicine. 8:514-523 |
| ISSN: | 1521-2254 1099-498X |
| DOI: | 10.1002/jgm.875 |
| Popis: | Background Systemic administration of non-viral gene therapy provides better access to tumors than local administration. Development of a promoter that restricts expression of cytotoxic proteins to the tumor vasculature will increase the safety of the system by minimizing expression in the non-dividing endothelial cells of the vasculature of non-target tissues. Methods Cell cycle promoters were tested for selective expression in dividing cells vs. non-dividing cells in vitro and promoter strength was compared to the cytomegalovirus (CMV) promoter. Successful promoter candidates were tested in vivo using two proliferating endothelium mouse models. Ovarectomized mice were injected with estradiol prior to lipoplex administration and expression levels were measured in the lungs and uterus 4 days after administration. The second model was a subcutaneous tumor model and expression levels were measured in the lungs and tumors. For both animal models, expression levels from the proliferating endothelium promoter were compared to that obtained from a CMV promoter. Results The results showed that the Cdc6 promoter yielded higher expression in proliferating vs. non-proliferating cells. Secondly, promoter strength could be selectively increased in endothelial cells by the addition of a multimerized endothelin enhancer (ET) to the Cdc6 promoter. Thirdly, comparison of expression levels in the lungs vs. uterus in the ovarectomized mouse model and lungs vs. tumor in the mouse tumor model showed expression was much higher in the uterus and the tumor than in the lungs for the ET/Cdc6 promoter, and expression levels were comparable to that of the CMV promoter in the hypervascularized tissues. Conclusions These results demonstrate that the combination of the endothelin enhancer with the Cdc6 promoter yields selective expression in proliferating endothelium and can be used to express cytotoxic proteins to treat vascularized tumors. Copyright © 2006 John Wiley & Sons, Ltd. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Plný text