国家重点基础研究发展计划(973)(2004CB518804),国家自然科学基金杰出青年项目(30325043),上海市视觉复明临床医学中心课题(FM040102-10),上海交通大学附属第一人民医院科学研究基金资助项目(03B02).
This work was supported by grants from National Basic Research Program of China (2004CB518804), The National Natural Science Foundation of China (30325043), Shanghai Clinical Medicine Center for Vision Rehabilitation (FM040102-10) and Foudation of First People's Hospital Affiliated Shanghai Jiaotong University(03B02).
视网膜母细胞瘤(retinoblastoma,RB)中由于Rb基因缺失或失活,转录调控因子E2F1始终处于活化状态,细胞不断增殖,E2F1活性增加是恶性肿瘤的普遍现象.根据人E2F1基因设计了3段shRNA,构建RNA干扰表达载体pSilencer-shE2F1,瞬时转染人视网膜母细胞瘤细胞株HXO-Rb-44和人肝癌细胞株SMMC-7721,通过荧光定量PCR检测E2F1表达水平的变化,PI (碘化丙锭)染色检测细胞周期各时相细胞数量以检测其对细胞周期的影响.根据筛选出的有效shRNA序列构建腺病毒载体并包装出腺病毒Ad-shE2F1,在裸鼠前房模型中,体外按50 moi的感染系数感染稳定表达绿色荧光蛋白(GFP)的人视网膜母细胞瘤细胞株48 h后,收集细胞,将2×105细胞注射到裸鼠眼前房内,连续观察眼内肿瘤细胞生长情况并拍照记录.通过转染肿瘤细胞株检测E2F1转录水平,筛选到1个能明显抑制肿瘤细胞内E2F1表达的shRNA序列,并使细胞周期中S期细胞数减少.经Ad-shE2F1感染的RB肿瘤细胞与对照相比较,其在裸鼠眼前房内肿瘤生长减缓.结果说明,有效抑制hE2F1表达的shRNA具有抑制体内外人视网膜母细胞瘤生长的作用.
The transcription factor E2F1 may form a complex with RB and which may play a major role in promoting growth control. Small interfering RNAs are short, double-stranded RNA molecules that can target mRNAs with complementary sequence for degradation via a cellular process to induce gene silence through degradation of homologous transcripts. The experiments were designed to inhibit proliferation of human retinoblastoma cells by knockdown human transcription factor E2F1 expression level using RNA interference technology. Three different hairpin shRNA inserts were designed targeting human transcription factor E2F1. The three inserts were synthesized and subcloned into a shRNA espression vector pSilencer H1puro which contains the H1 RNA polymerase Ⅲ promoter. The three plasmids encoding E2F1 short hairpin were transfected into human retinoblastoma cells line HXO-Rb-44 and human liver cancer cell line SMMC-7721 in vitro. Real-time RT-PCR was used to measure E2F1 mRNA level. For function analysis, propidium iodide (PI)-stained DNA content method was used to identify cell cycle by flow cytometer. The selected shE2F1 were cloned into an adenovirus system and packaged to adenovirus. Retinoblastoma HXO-Rb-44-gfp cell line which has been marked with green fluorescent protein (GFP) were infected by Ad-shE2F1 for 48h, and Ad-shNegative was used as control. The infected cells were injected into anterior chamber of nude mice eyes. The eyes were investigated and the consecutive and dynamic photos of the condition of RB tumor′s growth were taken by the special fluorescent microscope. One in three RNAi expression plasmids delivery resulted in 83.5% suppression of E2F1 mRNA transcription level. The same shRNA showed 89% inhibition in entering S phase. In nude mice eye anterior chamber, Ad-shE2F1 infected tumor cells grew more slowly than the negative control. The results showed that efficacy of Ad-shE2F1 were helpful in the process of limiting the growth of retinoblastoma. RNAi gene therapy directed against the human transcription factor E2F1 is a new therapeutic approach to suppress retinoblastoma cells proliferation.
王丰,马家烈,李惠明,陈霞芳,王煜非,黄倩.靶向E2F1的shRNA抑制眼内视网膜母细胞瘤生长[J].生物化学与生物物理进展,2009,36(5):587-591
复制生物化学与生物物理进展 ® 2025 版权所有 ICP:京ICP备05023138号-1 京公网安备 11010502031771号