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作者:
Zhang B, Feng X, Wang J, Xu X, Lin N, Liu H.
文题:
Combined antitumor effect of Ad-bFGF-siRNA and Ad-Vpr on the growth of xenograft glioma in nude mouse model.
期刊名,年份,卷(期),起止页码:
Pathol Oncol Res. 2011 Jun;17(2):237-42.
全文链接:
http://dx.doi.org/10.1007/s12253-010-9303-5
数据库名称:
springer
收录信息:
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eveb: 金币+5, ★★★★★最佳答案, thank 2014-11-13 12:27:03
jssxh: LS-EPI+1, 谢谢参与,请继续关注本版块 2014-11-13 14:59:39
Combined Antitumor Effect of Ad-bFGF-siRNA and Ad-Vpr on the Growth of Xenograft Glioma in Nude Mouse Model


作者:Zhang, B (Zhang, Biao)[ 2 ] ; Feng, XQ (Feng, Xuequan)[ 3 ] ; Wang, JH (Wang, Jinhuan)[ 1 ] ; Xu, XN (Xu, Xinnu)[ 4 ] ; Lin, N (Lin, Na)[ 4 ] ; Liu, HS (Liu, Hongsheng)[ 4 ]




PATHOLOGY & ONCOLOGY RESEARCH



卷: 17

期: 2

页: 237-242

DOI: 10.1007/s12253-010-9303-5

出版年: JUN 2011

查看期刊信息




































摘要

Basic fibroblast growth factor (bFGF) has been demonstrated to correlate with glioma grade and clinical outcome and has established its possible usefulness as a target for glioma therapy. Vpr has been described as an antitumor agent and displays a potent antitumor nature. Here, we try to investigate whether a combined treatment with bFGF-siRNA and Vpr gene would have a enhanced effectiveness on glioma in vitro and in vivo.After treatments with only Ad-bFGF-siRNA, only Ad-Vpr, and a combination of both, we assessed the changes in cell proliferation, cell cycle, and apoptosis in vitro by the methods of MTT, PI and FITC-AnnexinV double staining, respevtively. In addition, we also evaluated the combined effect of bFGF-siRNA and Vpr gene therapy on glioma in vivo using xenograft glioma models in nude mice. Combined Ad-bFGF-siRNA and Ad-Vpr treatment was more better successful in inhibiting cell proliferation in comparison with treatments of either Ad-bFGF-siRNA or Ad-Vpr alone. Treatment of Ad-Vpr alone or a treatment of a combination of Ad-bFGF-siRNA and Ad-Vpr induced the G2/M cell cycle arrest and apoptosis; however, combined treatment was more effective than the Ad-Vpr treatment alone. Although each single treatment can slow the growth of xenograft glioma, the combined treatment with Ad-bFGF-siRNA and Ad-Vpr was better than either the Ad-bFGF-siRNA or Ad-Vpr treatment alone. Our results suggest that the combination therapy with bFGF-siRNA and Vpr gene can achieve a enhanced activity of anti-glioma, supporting the idea that the combination of these two antitumor agents could open new perspectives in glioma therapy.


关键词

作者关键词:siRNA; bFGF; Vpr; Adenoviral vector

KeyWords Plus:IN-VIVO ELECTROPORATION; HIV-1 VPR; NUCLEAR ACCUMULATION; CELLS; GLIOBLASTOMA; INHIBITION; CASPASE-9; RECEPTOR; PLASMID; TUMORS


作者信息

通讯作者地址: Wang, JH (通讯作者)



      

Tianjin Huan Hu Hosp, Dept Neurosurg, 122 Qixiangtai Rd, Tianjin 300060, Peoples R China.



地址:



      

[ 1 ] Tianjin Huan Hu Hosp, Dept Neurosurg, Tianjin 300060, Peoples R China



      

[ 2 ] Tianjin Huan Hu Hosp, Clin Lab, Tianjin 300060, Peoples R China



      

[ 3 ] Tianjin First Ctr Hosp, Dept Neurosurg, Tianjin 300192, Peoples R China



      

[ 4 ] Tianjin First Ctr Hosp, Key Lab Crit Care Med, Minist Hlth, Tianjin 300192, Peoples R China



电子邮件地址:wangjinhuanfch@yahoo.com.cn


基金资助致谢



基金资助机构

授权号



National Natural Sciences Foundation of China


30672158

查看基金资助信息   




出版商

SPRINGER, VAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS


类别 / 分类

研究方向:Oncology; Pathology

Web of Science 类别:Oncology; Pathology


文献信息

文献类型:Article

语种:English

入藏号: WOS:000290587300007

PubMed ID: 20848251

ISSN: 1219-4956


期刊信息


Impact Factor (影响因子): Journal Citation Reports®


其他信息

IDS 号: 763VH

Web of Science 核心合集中的 "引用的参考文献": 20

Web of Science 核心合集中的 "被引频次": 5


引文网络




5 被引频次

20 引用的参考文献

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(数据来自 Web of ScienceTM 核心合集)



全部被引频次计数



5 / 所有数据库

5 / Web of Science 核心合集

1 / BIOSIS Citation Index

0 / 中国科学引文数据库

0 / Data Citation Index

0 / SciELO Citation Index


最近的引文









Zhang, S. HIV-1 viral protein R downregulates Ebp1 and stabilizes p53 in glioblastoma U87MG cells. CLINICAL & TRANSLATIONAL ONCOLOGY, MAR 2014.



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此记录来自:

Web of ScienceTM 核心合集


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如果希望提高此记录中数据的质量,请提供修正建议。
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入藏号: WOS:000290587300007
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