Abstract |
Interferon-gamma (IFN-γ) exhibits biological activities that are considered to have important roles in tumor suppression. Therefore, the IFN-γ gene is a potential candidate for in vivo cytokine gene therapy against skin cancer. The present study evaluated the efficacy of a hydrodynamics-based IFN-γ gene transfection for skin cancer treatment, in which the plasmid DNA encoding IFN-γ was administered into the tail vein of mice following 7,12-dimethylbenz[a] anthracene and 12-O-tetradecanoylphorbol-13-acetate-induced skin carcinogenesis. Serum levels of IFN-γ were substantially elevated without liver toxicity. The mice injected with IFN-γ plasmid DNA displayed a marked reduction in papilloma numbers, suppressed proliferation of epidermal cells and induction of caspase-3-mediated apoptosis. These results suggest that the hydrodynamics-based transfection of IFN-γ plasmid DNA is a convenient and efficient means of skin cancer gene therapy.
|
Authors | J-H Ko, B-G Jung, Y-S Park, B-J Lee |
Journal | Cancer gene therapy
(Cancer Gene Ther)
Vol. 18
Issue 9
Pg. 646-54
(Sep 2011)
ISSN: 1476-5500 [Electronic] England |
PMID | 21799530
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- 9,10-Dimethyl-1,2-benzanthracene
- Interferon-gamma
- Caspase 3
- Tetradecanoylphorbol Acetate
|
Topics |
- 9,10-Dimethyl-1,2-benzanthracene
(toxicity)
- Animals
- Apoptosis
(genetics)
- Caspase 3
(genetics, metabolism)
- Cell Proliferation
- Female
- Genetic Therapy
- Interferon-gamma
(genetics, metabolism)
- Mice
- Mice, Inbred BALB C
- Plasmids
- Skin Neoplasms
(chemically induced, therapy)
- Tetradecanoylphorbol Acetate
(toxicity)
|