Saha Debabrata, Dunn Henry, Zhou Heling, Harada Hiroshi, Hiraoka Masahiro, Mason Ralph P, Zhao Dawen
Department of Radiation Oncology, University of Texas Southwestern Medical Center, USA.
J Vis Exp. 2011 Oct 3(56):3175. doi: 10.3791/3175.
It is well recognized that tumor hypoxia plays an important role in promoting malignant progression and affecting therapeutic response negatively. There is little knowledge about in situ, in vivo, tumor hypoxia during intracranial development of malignant brain tumors because of lack of efficient means to monitor it in these deep-seated orthotopic tumors. Bioluminescence imaging (BLI), based on the detection of light emitted by living cells expressing a luciferase gene, has been rapidly adopted for cancer research, in particular, to evaluate tumor growth or tumor size changes in response to treatment in preclinical animal studies. Moreover, by expressing a reporter gene under the control of a promoter sequence, the specific gene expression can be monitored non-invasively by BLI. Under hypoxic stress, signaling responses are mediated mainly via the hypoxia inducible factor-1α (HIF-1α) to drive transcription of various genes. Therefore, we have used a HIF-1α reporter construct, 5HRE-ODD-luc, stably transfected into human breast cancer MDA-MB231 cells (MDA-MB231/5HRE-ODD-luc). In vitro HIF-1α bioluminescence assay is performed by incubating the transfected cells in a hypoxic chamber (0.1% O₂) for 24 hr before BLI, while the cells in normoxia (21% O₂) serve as a control. Significantly higher photon flux observed for the cells under hypoxia suggests an increased HIF-1α binding to its promoter (HRE elements), as compared to those in normoxia. Cells are injected directly into the mouse brain to establish a breast cancer brain metastasis model. In vivo bioluminescence imaging of tumor hypoxia dynamics is initiated 2 wks after implantation and repeated once a week. BLI reveals increasing light signals from the brain as the tumor progresses, indicating increased intracranial tumor hypoxia. Histological and immunohistochemical studies are used to confirm the in vivo imaging results. Here, we will introduce approaches of in vitro HIF-1α bioluminescence assay, surgical establishment of a breast cancer brain metastasis in a nude mouse and application of in vivo bioluminescence imaging to monitor intracranial tumor hypoxia.
众所周知,肿瘤缺氧在促进恶性进展和对治疗反应产生负面影响方面起着重要作用。由于缺乏在这些深部原位肿瘤中监测肿瘤缺氧的有效手段,对于恶性脑肿瘤颅内发展过程中的原位、体内肿瘤缺氧情况了解甚少。基于检测表达荧光素酶基因的活细胞发出的光的生物发光成像(BLI)已迅速应用于癌症研究,特别是在临床前动物研究中评估肿瘤生长或肿瘤大小对治疗的反应。此外,通过在启动子序列控制下表达报告基因,可通过BLI非侵入性地监测特定基因表达。在缺氧应激下,信号反应主要通过缺氧诱导因子-1α(HIF-1α)介导,以驱动各种基因的转录。因此,我们使用了一种稳定转染入人乳腺癌MDA-MB231细胞(MDA-MB231/5HRE-ODD-luc)的HIF-1α报告基因构建体5HRE-ODD-luc。体外HIF-1α生物发光测定是在进行BLI之前,将转染细胞置于缺氧箱(0.1% O₂)中孵育24小时,而常氧(21% O₂)中的细胞作为对照。与常氧中的细胞相比,缺氧条件下的细胞观察到显著更高的光子通量,表明HIF-1α与其启动子(HRE元件)的结合增加。将细胞直接注射到小鼠脑内以建立乳腺癌脑转移模型。在植入后2周开始对肿瘤缺氧动态进行体内生物发光成像,并每周重复一次。BLI显示随着肿瘤进展,来自脑内的光信号增加,表明颅内肿瘤缺氧增加。组织学和免疫组织化学研究用于证实体内成像结果。在此,我们将介绍体外HIF-1α生物发光测定方法、裸鼠乳腺癌脑转移的手术建立方法以及应用体内生物发光成像监测颅内肿瘤缺氧的方法。