Abstract |
We constructed an adeno-associated virus (AAV) vector containing the human interferon-beta (HuIFN-b ) gene (AAV-IFN-beta) and investigated its antitumor effect against human glioma cells (U251-SP) inoculated into the brain of nude mice. Prior to this, we examined human glioma cells transduced with AAV-IFN-beta using video-enhanced contrast differential interference contrast (VEC- DIC) microscopy. Infection of AAV-IFN-beta induced apoptosis and secondary necrosis in human glioma cells. In in vivo experiments, we confirmed production of HuIFN-beta and induction of heat-shock protein (HSP) in glioma cells transduced with AAV-IFN-beta. Growth of the experimental gliomas was completely inhibited by six injections of AAV-IFN-beta, starting 7 days after transplantation of glioma cells. In addition, the survival of mice treated with AAV-IFN-beta was remarkably prolonged. These results indicate that AAV-IFN-beta induces apoptosis of glioma cells and has a strong antitumor effect in this experimental glioma model.
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Authors | Jun Yoshida, Masaaki Mizuno, Norimoto Nakahara, Peter Colosi |
Journal | Japanese journal of cancer research : Gann
(Jpn J Cancer Res)
Vol. 93
Issue 2
Pg. 223-8
(Feb 2002)
ISSN: 0910-5050 [Print] Japan |
PMID | 11856487
(Publication Type: Journal Article)
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Chemical References |
- Heat-Shock Proteins
- Interferon-beta
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Topics |
- Animals
- Brain Neoplasms
(pathology, therapy)
- Dependovirus
(genetics)
- Female
- Genetic Therapy
- Genetic Vectors
- Glioma
(pathology, therapy)
- Heat-Shock Proteins
(genetics)
- Humans
- Interferon-beta
(genetics)
- Mice
- Mice, Inbred BALB C
- Mice, Nude
- Neoplasm Transplantation
- Tumor Cells, Cultured
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