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用于测量神经纤维瘤病小鼠模型中肿瘤生长的生物发光方法。

Bioluminescent approaches for measuring tumor growth in a mouse model of neurofibromatosis.

作者信息

Hawes Jessica J, Reilly Karlyne M

机构信息

Mouse Cancer Genetics Program, National Cancer Institute, Frederick, Maryland 21702, USA.

出版信息

Toxicol Pathol. 2010 Jan;38(1):123-30. doi: 10.1177/0192623309357075.

Abstract

Neurofibomatosis (NF1) patients are susceptible to multiple tumors of the nervous system including neurofibromas, optic glioma, malignant peripheral nerve sheath tumors (MPNSTs), and astrocytoma. The Nf1+/-;Trp53+/- (NPcis) mouse model of NF1 spontaneously develops astrocytoma and MPNSTs that are very similar to human NF1 tumors. To use this model for testing potential therapeutics, we have developed systems that take advantage of bioluminescent reporters of tumor growth. We have generated E2F1 promoter-driving luciferase (ELUX) reporter mice to detect proliferating tumors in NPcis mice in vivo using bioluminescence. The power of this system is that it enables looking at tumor evolution and detecting spontaneous tumors at early stages of development as they evolve within their natural haploinsufficient microenvironment. This system can be used to identify tumors at different stages of tumorigenesis and to examine where spontaneous NF1 tumors initiate. The ability to rapidly screen multiple animals at a time increases the potential for use of this model in preclinical trials. This model will be valuable for the characterization of spontaneous NF1 tumors and will be important for studying the treatment and prevention of NF1 tumors in vivo.

摘要

神经纤维瘤病1型(NF1)患者易患多种神经系统肿瘤,包括神经纤维瘤、视神经胶质瘤、恶性外周神经鞘瘤(MPNST)和星形细胞瘤。NF1的Nf1+/-;Trp53+/-(NPcis)小鼠模型会自发形成与人类NF1肿瘤非常相似的星形细胞瘤和MPNST。为了利用该模型测试潜在疗法,我们开发了利用肿瘤生长生物发光报告基因的系统。我们构建了E2F1启动子驱动荧光素酶(ELUX)报告基因小鼠,以利用生物发光在体内检测NPcis小鼠中的增殖肿瘤。该系统的优势在于,它能够观察肿瘤的演变,并在自发肿瘤在其自然单倍体不足微环境中演变时,在发育早期检测到它们。该系统可用于识别肿瘤发生不同阶段的肿瘤,并检查自发NF1肿瘤的起始部位。一次快速筛选多只动物的能力增加了该模型在临床前试验中使用的潜力。该模型对于表征自发NF1肿瘤将具有重要价值,并且对于研究体内NF1肿瘤的治疗和预防也将具有重要意义。

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