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优化用于放射遗传癌症治疗的辐射反应性基因启动子。

Optimizing radiation-responsive gene promoters for radiogenetic cancer therapy.

作者信息

Scott S D, Joiner M C, Marples B

机构信息

Department of Experimental Radiation Oncology, Gray Cancer Institute, Northwood, Middlesex, UK.

出版信息

Gene Ther. 2002 Oct;9(20):1396-402. doi: 10.1038/sj.gt.3301822.

Abstract

We have been developing synthetic gene promoters responsive to clinical doses of ionizing radiation (IR) for use in suicide gene therapy vectors. The crucial DNA sequences utilized are units with the consensus motif CC(A/T)(6)GG, known as CArG elements, derived from the IR-responsive Egr1 gene. In this study we have investigated the parameters needed to enhance promoter activation to radiation. A series of plasmid vectors containing different enhancer/promoters were constructed, transiently transfected into tumor cells (MCF-7 breast adenocarcinoma and U-373MG glioblastoma) and expression of a downstream reporter assayed. Results revealed that increasing the number of CArG elements, up to a certain level, increased promoter radiation-response; from a fold-induction of 1.95 +/- 0.17 for four elements to 2.74 +/- 0.17 for nine CArGs of the same sequence (for MCF-7 cells). Specific alteration of the core A/T sequences caused an even greater positive response, with fold-inductions of 1.71 +/- 0.23 for six elements of prototype sequence compared with 2.96 +/- 0.52 for one of the new sequences following irradiation. Alteration of spacing (from six to 18 nucleotides) between elements had little effect, as did the addition of an adjacent Sp1 binding site. Combining the optimum number and sequence of CArG elements in an additional enhancer was found to produce the best IR induction levels. Furthermore, the improved enhancers also performed better than the previously reported prototype when used in in vitro and in vivo experimental GDEPT. We envisage such enhancers will be used to drive suicide gene expression from vectors delivered to a tumor within an irradiated field. The modest, but tight expression described in the present study could be amplified using a molecular 'switch' system as previously described using Cre/LoxP. In combination with targeted delivery, this strategy has great potential for significantly improving the efficacy of cancer treatment in the large number of cases where radiotherapy is currently employed.

摘要

我们一直在研发对临床剂量的电离辐射(IR)有反应的合成基因启动子,用于自杀基因治疗载体。所利用的关键DNA序列是具有共有基序CC(A/T)(6)GG的单元,即所谓的CArG元件,其源自对IR有反应的Egr1基因。在本研究中,我们研究了增强启动子对辐射激活所需的参数。构建了一系列含有不同增强子/启动子的质粒载体,将其瞬时转染到肿瘤细胞(MCF-7乳腺腺癌和U-373MG胶质母细胞瘤)中,并检测下游报告基因的表达。结果显示,增加CArG元件的数量,在一定程度内,会增加启动子对辐射的反应;对于相同序列的四个元件,倍数诱导为1.95±0.17,而对于九个CArG元件,倍数诱导为2.74±0.17(针对MCF-7细胞)。核心A/T序列的特定改变引起了更大的阳性反应,照射后,原型序列的六个元件的倍数诱导为1.71±0.23,而新序列之一的倍数诱导为2.96±0.52。元件之间间隔的改变(从六个到18个核苷酸)影响不大,添加相邻的Sp1结合位点也是如此。发现在额外的增强子中组合最佳数量和序列的CArG元件可产生最佳的IR诱导水平。此外,在体外和体内实验性基因导向酶解药物前体疗法(GDEPT)中使用时,改进后的增强子也比先前报道的原型表现更好。我们设想此类增强子将用于驱动递送至照射野内肿瘤的载体中的自杀基因表达。本研究中描述的适度但严格的表达可以使用如先前使用Cre/LoxP所描述的分子“开关”系统进行放大。与靶向递送相结合,该策略在目前采用放射治疗的大量病例中具有显著提高癌症治疗疗效的巨大潜力。

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