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作者: Feng X, Zhang B, Wang J, Xu X, Lin N, Liu H. 文题: Adenovirus-mediated transfer of siRNA against basic fibroblast growth factor mRNA enhances the sensitivity of glioblastoma cells to chemotherapy. 期刊名,年份,卷(期),起止页码: Med Oncol. 2011 Mar;28(1):24-30. 全文链接: http://dx.doi.org/10.1007/s12032-010-9445-z 数据库名称: springer 收录信息: 求助 SCI 收录信息 求助被引次数 |
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baiyuefei
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风雪
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入藏号: WOS:000287756000004 4次被引用： https://apps.webofknowledge.com/ ... FromNonInterProduct 1. Blocking the bFGF/STAT3 interaction through specific signaling pathways induces apoptosis in glioblastoma cells 作者: Wu, Jingchao; Feng, Xuequan; Zhang, Biao; 等. JOURNAL OF NEURO-ONCOLOGY 卷: 120 期: 1 页: 33-41 出版年: OCT 2014 出版商处的全文 查看摘要 被引频次: 0 (来自 Web of Science 的核心合集) 2. The role of basic fibroblast growth factor in glioblastoma multiforme and glioblastoma stem cells and in their in vitro culture 作者: Haley, Elizabeth M.; Kim, Yonghyun CANCER LETTERS 卷: 346 期: 1 页: 1-5 出版年: APR 28 2014 出版商处的全文 查看摘要 被引频次: 0 (来自 Web of Science 的核心合集) 3. Basic fibroblast growth factor upregulates survivin expression in hepatocellular carcinoma cells via a protein kinase B-dependent pathway 作者: Sun, Bo; Xu, Haiyan; Zhang, Gang; 等. ONCOLOGY REPORTS 卷: 30 期: 1 页: 385-390 出版年: JUL 2013 出版商处的全文 查看摘要 被引频次: 0 (来自 Web of Science 的核心合集) 4. MicroRNA and Diseases of the Nervous System 作者: Omahen, David A. NEUROSURGERY 卷: 69 期: 2 页: 440-454 出版年: AUG 2011 出版商处的全文 查看摘要 |
3楼2014-11-13 12:26:46
baiyuefei
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感谢参与，应助指数 +1
eveb: 金币+5, ★★★★★最佳答案, thanks 2014-11-13 12:32:24
jssxh: LS-EPI+1, 谢谢参与，请继续关注本版块 2014-11-13 14:59:25
感谢参与，应助指数 +1
eveb: 金币+5, ★★★★★最佳答案, thanks 2014-11-13 12:32:24
jssxh: LS-EPI+1, 谢谢参与，请继续关注本版块 2014-11-13 14:59:25
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https://apps.webofknowledge.com/ ... age=1&doc=1 Adenovirus-mediated transfer of siRNA against basic fibroblast growth factor mRNA enhances the sensitivity of glioblastoma cells to chemotherapy 作者:Feng, XQ (Feng, Xuequan)[ 1 ] ; Zhang, BA (Zhang, Biao)[ 2 ] ; Wang, JH (Wang, Jinhuan)[ 1,2 ] ; Xu, XN (Xu, Xinnv)[ 2 ] ; Lin, N (Lin, Na)[ 2 ] ; Liu, HS (Liu, Hongsheng)[ 2 ] MEDICAL ONCOLOGY 卷: 28 期: 1 页: 24-30 DOI: 10.1007/s12032-010-9445-z 出版年: MAR 2011 查看期刊信息 摘要 Basic fibroblast growth factor (bFGF) is an important growth factor for glioma cell proliferation and invasion. BFGF is overexpressed in malignant gliomas and its level is associated with malignant grades and clinical outcome of patients with gliomas. Small interfering RNAs (siRNA) are synthetic forms of microRNA made of short double stranded RNA, and they effectively catalyze the degradation of their target mRNA. The use of siRNA has become a key method in the suppression of gene expression and the development of therapeutic agents. In this study, we used an adenovirus(Ad)-mediated transfer of siRNA against bFGF mRNA (Ad-bFGF-siRNA) to study the effect of down-regulating bFGF expression on the sensitivity of glioma cells to chemotherapeutics. An optimal siRNA sequence specific for bFGF mRNA was cloned into an adenoviral vector and transfected into three glioma cell lines: U251, A172, and LN229. Methyl thiazolyl tetrazolium (MTT) assays were used to examine changes in cell proliferation, and changes in bFGF mRNA and protein levels in U251 cells were detected using quantitative RT-PCR and Western blot, respectively. Apoptosis of U251 cells was detected using Hoechst staining and flow cytometry, with expression of apoptosis-related proteins evaluated by Western blot. Following the transfection of a bFGF-specific siRNA, mRNA and protein levels of bFGF decreased significantly. Lower rates of proliferation and increased levels of apoptosis also were associated with the Ad-bFGF-siRNA-transfected group compared to control group. Decreased expression of Bcl-2, Bcl-xL, Jak-1, and STAT-3 and increased expression of Bax also were detected in the Ad-bFGF-siRNA-transfected group. For cells treated with both Ad-bFGF-siRNA and chemotherapeutics, a significant reduction in cell survival was observed compared to treatment with Ad-bFGF-siRNA or chemotherapeutics alone. Overall, we found that targeting bFGF mRNA with a siRNA resulted in lower rates of proliferation, increased apoptosis, and enhanced sensitivity of glioma cells to chemotherapy drugs. This suggests that specific targeting of bFGF mRNA may provide a novel approach for the treatment of glioblastoma multiforme (GBM). 关键词 作者关键词:bFGF; Apoptosis; RNA interference; GBM KeyWords Plus:C6 GLIOMA-CELLS; NUCLEAR ACCUMULATION; INHIBITION; EXPRESSION; APOPTOSIS; MECHANISMS; RECEPTOR 作者信息 通讯作者地址: Wang, JH (通讯作者) Tianjin First Ctr Hosp, Dept Neurosurg, Fukang Rd 24, Tianjin 300192, Peoples R China. 地址: [ 1 ] Tianjin First Ctr Hosp, Dept Neurosurg, Tianjin 300192, Peoples R China [ 2 ] 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 HUMANA PRESS INC, 999 RIVERVIEW DRIVE SUITE 208, TOTOWA, NJ 07512 USA 类别 / 分类 研究方向:Oncology Web of Science 类别:Oncology 文献信息 文献类型:Article 语种:English 入藏号: WOS:000287756000004 PubMed ID: 20221717 ISSN: 1357-0560 期刊信息 Impact Factor (影响因子): Journal Citation Reports® 其他信息 IDS 号: 726VZ Web of Science 核心合集中的 "引用的参考文献": 21 Web of Science 核心合集中的 "被引频次": 4 |
2楼2014-11-13 12:25:55