Inhibitory Effects of Decoy-ODN Targeting Activated STAT3 on Human Glioma Growth In Vivo

被引:1
|
作者
Shen, Jie [1 ]
Li, Ronghui [1 ]
Li, Gang [1 ]
机构
[1] Shandong Univ, Qi Lu Hosp, Dept Neurosurg, Jinan 250012, Shandong, Peoples R China
来源
IN VIVO | 2009年 / 23卷 / 02期
关键词
Glioma; STAT3; decoy-ODN; in vivo; KAPPA-B ACTIVATION; CONSTITUTIVE ACTIVATION; NEOINTIMAL FORMATION; SIGNAL TRANSDUCER; CARCINOMA CELLS; OLIGONUCLEOTIDES; VITRO; OLIGODEOXYNUCLEOTIDES; TRANSCRIPTION-3; INVASION;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: It has been previously found that a constitutively activated signal transducer and activator of transcription 3 (STAT3) blocked by decoy-ODN led to glioma growth inhibition in vitro. The objectives of this study were to identify whether STAT3 decoy-ODN had the same effect or not in vivo. Materials and Methods: Western blot was used to detect p-STAT3 in glioma and normal brain tissue. U251 cells were subcutaneously injected into nude mice and decoy-ODN was intratumorally administrated. TUNEL was used to exam the apoptosis cells in xenografts. Genes regulated by STAT3 were evaluated by RT-PCR and immunohistochemistry. Results: Activated STAT3 was highly present in glioma but not normal brain tissues. STAT3 decoy-ODN could significantly suppress the growth of glioma by inhibiting proliferation and promoting apoptosis in xenografts. The target genes controlled by STAT3 were down-regulated at both transcription and translation levels. Conclusion: The present study suggested that decoy-ODN provide an effective therapeutic approach to treat glioma in vivo.
引用
收藏
页码:237 / 243
页数:7
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