小剂量5-FU提高携带VEGF siRNA的腺病毒载体对肿瘤细胞的转导效率和基因治疗效果的研究(英文)

作     者：王丰 李惠明 陈霞芳 Feng Wang;Hui-Ming Li;Xia-Fang Chen;Kuang-Cheng Xie;Qian Huang

作者机构：Experimental CenterAffiliated First People's HospitalShanghai Jiaotong University 

基　　金：National Science Fund for Distinguished Young Scholars (No.30325043) Major State Basic Research Development Program of China(No. 2004CB518804) 

出 版 物：《Chinese Journal of Cancer》 (CHINESE JOURNAL OF CANCER)

年 卷 期：2010年第29卷第7期

页      码：677-682页

摘      要：Background and Objective:Adenovirus vectors were widely used in gene therapy for *** used adenovirus vector to transfer small interfering RNA(siRNA) against vascular epithelium growth factor A(VEGF-A) molecules to mouse lung adenoma LA795 cells and used low dose of chemotherapeutic drugs to further elevate the infection efficiency of adenovirus vector in and therapeutic effect of RNAi on tumor *** hods:LA795 cells were infected by Ad/EGFP and treated with different dosages of gemcitabin,epirubicin,cisplatin,or 5-fluorouracil(5-FU).Cells were observed under fluorescence microscope continuously using green fluorescent protein(GFP) as the reporter *** percentage of GFP-positive cells and fluorescent intensity were tested by flow cytometry to determine optimum concentrations of ***/siVEGF-A containing VEGF-A siRNA was ***-time PCR and ELISA were applied to measure the expression level of VEGF-A after LA795 cells were infected by Ad/siVEGF-A and treated with *** combination of Ad/siVEGF-A and 5-FU was also applied in treating subcutaneous tumor in *** s:Low dose of 5FU elevated the Ad/EGFP infection in LA795 cells significantly,and also enhanced the effect of Ad/siVEGF-A in downregulating VEGF-A mRNA and protein levels in tumor *** used in tumor in vivo,the combination strategy repressed tumor growth ***:Low dose of 5-FU can enhance the capability of adenovirus infecting tumor cells and promote the efficiency of gene therapy by adenovirus.

主 题 词：血管内皮生长因子 广告效果 肿瘤生长 氟尿嘧啶 肺腺癌 低剂量 细胞株 转染效率 

学科分类：1002[医学-临床医学类] 100214[100214] 10[医学] 

核心收录：

D　O　I：10.5732/cjc.009.10684

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