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一种用于研究人乳腺癌细胞中NF-κB活性和细胞凋亡的新型多色生物发光成像平台。

A new multicolor bioluminescence imaging platform to investigate NF-κB activity and apoptosis in human breast cancer cells.

作者信息

Mezzanotte Laura, An Na, Mol Isabel M, Löwik Clemens W G M, Kaijzel Eric L

机构信息

Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.

Department of Endocrinology, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

PLoS One. 2014 Jan 17;9(1):e85550. doi: 10.1371/journal.pone.0085550. eCollection 2014.

DOI:10.1371/journal.pone.0085550
PMID:24465597
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3894999/
Abstract

BACKGROUND

Evaluation of novel drugs for clinical development depends on screening technologies and informative preclinical models. Here we developed a multicolor bioluminescent imaging platform to simultaneously investigate transcription factor NF-κB signaling and apoptosis.

METHODS

The human breast cancer cell line (MDA-MB-231) was genetically modified to express green, red and blue light emitting luciferases to monitor cell number and viability, NF-κB promoter activity and to perform specific cell sorting and detection, respectively. The pro-luciferin substrate Z-DEVD-animoluciferin was employed to determine apoptotic caspase 3/7 activity. We used the cell line for the in vitro evaluation of natural compounds and in vivo optical imaging of tumor necrosis factor TNFα-induced NF-κB activation.

RESULTS

Celastrol, resveratrol, sulphoraphane and curcumin inhibited the NF-κB promoter activity significantly and in a dose dependent manner. All compounds except resveratrol induced caspase 3/7 dependent apoptosis. Multicolor bioluminescence in vivo imaging allowed the investigation of tumor growth and NF-κB induction in a mouse model of breast cancer.

CONCLUSION

Our new method provides an imaging platform for the identification, validation, screening and optimization of compounds acting on NF-κB signaling and apoptosis both in vitro and in vivo.

摘要

背景

新型药物临床开发的评估依赖于筛选技术和信息丰富的临床前模型。在此,我们开发了一种多色生物发光成像平台,用于同时研究转录因子NF-κB信号传导和细胞凋亡。

方法

对人乳腺癌细胞系(MDA-MB-231)进行基因改造,使其表达绿色、红色和蓝色发光荧光素酶,分别用于监测细胞数量和活力、NF-κB启动子活性以及进行特定的细胞分选和检测。使用促荧光素底物Z-DEVD-氨基荧光素测定凋亡的半胱天冬酶3/7活性。我们使用该细胞系对天然化合物进行体外评估,并对肿瘤坏死因子TNFα诱导的NF-κB激活进行体内光学成像。

结果

雷公藤红素、白藜芦醇、萝卜硫素和姜黄素均能显著且呈剂量依赖性地抑制NF-κB启动子活性。除白藜芦醇外,所有化合物均诱导半胱天冬酶3/7依赖性细胞凋亡。多色生物发光体内成像可在乳腺癌小鼠模型中研究肿瘤生长和NF-κB诱导情况。

结论

我们的新方法提供了一个成像平台,可用于在体外和体内鉴定、验证、筛选和优化作用于NF-κB信号传导和细胞凋亡的化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/356c/3894999/e7edecbfb3aa/pone.0085550.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/356c/3894999/e7edecbfb3aa/pone.0085550.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/356c/3894999/e7edecbfb3aa/pone.0085550.g003.jpg

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