Induction of apoptosis by tumor necrosis factor receptors 2 transgene in human laryngeal squamous cacinoma in nude mice animal model.
- Author:
Hongxia LI
1
;
Xiaoming LI
;
Xiaoping GAO
;
Xiuying LU
Author Information
1. Department of Otorhinolaryngology Head and Neck Surgery, Bethune International Peace Hospital, Shijiazhuang, 050082, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Apoptosis;
drug effects;
Carcinoma, Squamous Cell;
pathology;
therapy;
Cell Line, Tumor;
Genetic Therapy;
methods;
Humans;
Laryngeal Neoplasms;
pathology;
therapy;
Mice;
Mice, Nude;
Receptors, Tumor Necrosis Factor, Type II;
genetics;
pharmacology;
Transfection;
Transgenes;
Tumor Necrosis Factor-alpha;
genetics;
pharmacology
- From:
Journal of Clinical Otorhinolaryngology Head and Neck Surgery
2009;23(3):125-129
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the effect of tumor necrosis factor receptors II (TNFR II) in vivo transgene with topical injection of TNF alpha in inducing apoptosis and cell killing of laryngeal squamous carcinoma in nude mice animal model.
METHOD:Laryngeal carcinoma implantation animal model was established on nude mice. In vivo gene transfection of TNFR II was carried out using liposome as a carrier. TNF alpha was topically injected into tumor. Goss measurement of tumor, flow cytometry, immunohistochemistry, tunel and transmission electron microscopy were conducted to observe the expression of TNFR II protein and the apoptosis of tumor cells, and the effects of tumor killing and growth inhibition was objectively evaluated.
RESULT:Nude mice models bearing laryngeal carcinoma was established in 94.5% animals. After in vivo gene transfection, the expression of TNFR II protein reach the highest level at 48 hours, and remain in a substantially high level within 72 hours. Immunohistochemistry showed the expression of TNFR II is mainly on the cell membrane of the transfected tumor cells. Topical injection of 2000 U TNF alpha was most efficient in inducing tumor cell apoptosis, cell inhibition and cell killing. The tumor volume, weight, and tumor/body ratio in TNFR II transfected group were (1161.333 +/- 166.555) mm3, (1.100 +/- 0.832) g and 0.044 +/- 0.332, respectively, with a corresponding high level of tumor cell apoptosis rate (38.226 +/- 13.671) %, all of which were significantly higher than that in non-transfected group. Tunel and ultrastructural observations demonstrated apoptosis-related changes in the transfected tumor cells.
CONCLUSION:Up-regulation of TNFR II expression by in vivo gene transfection on tumor cells can remarkably enhance the tumor cell killing effect of topical injection of TNF-alpha. In vivo transgene of TNFR II in combination with topical injection of TNF alpha may become a effective gene therapy method in treating laryngeal cancer.
