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硝基还原酶,一种用于转移性癌症体内时域光学成像的近红外报告平台。

Nitroreductase, a near-infrared reporter platform for in vivo time-domain optical imaging of metastatic cancer.

机构信息

Institute of Medicine, Hematology Section; Department of Biomedicine, University of Bergen, Norway.

出版信息

Cancer Res. 2013 Feb 15;73(4):1276-86. doi: 10.1158/0008-5472.CAN-12-2649. Epub 2012 Dec 10.

Abstract

The ability to visualize reporter gene expression in vivo has revolutionized all facets of biologic investigation and none more so than imaging applications in oncology. Near-infrared reporter gene imaging may facilitate more accurate evaluation of chemotherapeutic response in preclinical models of orthotopic and metastatic cancers. We report the development of a cell permeable, quenched squarine probe (CytoCy5S), which is reduced by Escherichia coli nitroreductase (NTR), resulting in a near-infrared fluorescent product. Time-domain molecular imaging of NTR/CytoCy5S reporter platform permitted noninvasive monitoring of disease progression in orthotopic xenografts of disseminated leukemia, lung, and metastatic breast cancer. This methodology facilitated therapeutic evaluation of NTR gene-directed enzymatic prodrug therapy with conventional metronidazole antibiotics. These studies show NTR/CytoCy5S as a near-infrared gene reporter system with broad preclinical and prospective clinical applications within imaging, and gene therapy, of cancer.

摘要

活体可视化报告基因表达的能力彻底改变了生物学研究的各个方面,在肿瘤学的成像应用中更是如此。近红外报告基因成像可能有助于更准确地评估原位和转移性癌症的临床前模型中的化疗反应。我们报告了一种细胞通透性、猝灭的 squarine 探针(CytoCy5S)的开发,该探针可被大肠杆菌硝基还原酶(NTR)还原,生成近红外荧光产物。NTR/CytoCy5S 报告平台的时域分子成像允许非侵入性监测播散性白血病、肺癌和转移性乳腺癌的原位异种移植物中的疾病进展。这种方法促进了 NTR 基因指导的酶前药治疗与传统甲硝唑抗生素的治疗评估。这些研究表明 NTR/CytoCy5S 是一种近红外基因报告系统,具有广泛的临床前和潜在的临床应用,可用于癌症的成像和基因治疗。

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