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Illuminating cancer systems with genetically engineered mouse models and coupled luciferase reporters in vivo

机译:利用基因工程小鼠模型和偶联的萤光素酶报道分子在体内照亮癌症系统

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摘要

Bioluminescent imaging (BLI) is a powerful noninvasive tool that has dramatically accelerated the in vivo interrogation of cancer systems and longitudinal analysis of mouse models of cancer over the past decade. Various luciferase enzymes have been genetically engineered into mouse models (GEMM) of cancer, which permit investigation of cellular and molecular events associated with oncogenic transcription, posttranslational processing, protein-protein interactions, transformation, and oncogene addiction in live cells and animals. Luciferase-coupled GEMMs ultimately serve as a noninvasive, repetitive, longitudinal, and physiologic means by which cancer systems and therapeutic responses can be investigated accurately within the autochthonous context of a living animal. Significance: Luciferase-dependent bioluminescence imaging coupled with genetically engineered mouse models of cancer permit interrogation of tumor biology and therapeutic response within the proper physiological context of the whole animal in vivo.
机译:生物发光成像(BLI)是一种功能强大的非侵入性工具,在过去十年中,该工具极大地加速了对癌症系统的体内询问和对小鼠癌症模型的纵向分析。多种萤光素酶已被遗传工程改造为癌症的小鼠模型(GEMM),从而可以研究与活细胞和动物中的致癌转录,翻译后加工,蛋白质-蛋白质相互作用,转化和致癌基因成瘾有关的细胞和分子事件。萤光素酶偶联的GEMM最终作为一种非侵入性,重复性,纵向和生理手段,可通过该手段在活体动物的自然环境中准确地调查癌症系统和治疗反应。意义:依赖于荧光素酶的生物发光成像与基因工程改造的小鼠癌症模型相结合,可以在整个动物体内正确的生理环境下审视肿瘤生物学和治疗反应。

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