Department of Anatomy and Cell Biology, Osaka Medical College, Takatsuki, Osaka 569-8686, Japan.
Anticancer Res. 2009 Nov;29(11):4389-95.
Many areas of research, including gene and pharmacological therapeutics, would benefit from longitudinal in vivo monitoring methodologies. To investigate the feasibility of one such methodology, we developed a murine mammary cancer model amenable to sequential bioluminescent imaging of tumor growth and metastasis in living animals.
Metastatic mouse mammary carcinoma BJMC3879 cells were transfected to stably express firefly luciferase and inoculated into immunocompetent female BALB/c mice.
Sequential analysis using bioluminescent imaging showed increasing photon counts correlated to expanding mammary tumor volumes; in addition, strong signals from axillary, mandibular, femoral, thoracic and abdominal regions in mice were histopathologically determined to be due to metastases, the majority of which occurred in lymph nodes and lungs.
The bioluminescent mouse mammary cancer model we established provides a method for quantifiable longitudinal in vivo imaging that can be used in gene and pharmacological therapy applications.
包括基因和药物治疗学在内的许多研究领域都将受益于纵向体内监测方法。为了研究这种方法的可行性,我们开发了一种适用于活体动物中肿瘤生长和转移的连续生物发光成像的鼠乳腺肿瘤模型。
将转移性鼠乳腺癌细胞 BJMC3879 转染以稳定表达萤火虫荧光素酶,并接种到免疫功能正常的雌性 BALB/c 小鼠中。
使用生物发光成像进行的连续分析显示,光子计数的增加与乳腺肿瘤体积的扩大相关;此外,在小鼠的腋窝、下颌、股骨、胸部和腹部区域的强信号通过组织病理学确定是转移所致,其中大多数发生在淋巴结和肺部。
我们建立的生物发光鼠乳腺肿瘤模型提供了一种可用于基因和药物治疗应用的定量纵向体内成像方法。