Kaneko K, Yano M, Tsujinaka T, Morita S, Taniguchi M, Fujiwara Y, Doki Y, Inoue M, Shiozaki H, Monden M
Department of Surgery and Clinical Oncology, Osaka University Graduate School of Medicine, E-2, Suita, Osaka 565-0871, Japan.
Int J Oncol. 2000 May;16(5):893-8. doi: 10.3892/ijo.16.5.893.
To establish a visible peritoneal micrometastatic model, an enhanced green fluorescent protein (EGFP) expressing plasmid vector was transfected into the gastric cancer cell line, MKN-45. Highly expressing EGFP cells were injected into the peritoneal cavity of nude mice. Then, the peritoneum and abdominal organs were harvested and observed on days 1, 4 and 7. Fluorescence stereomicroscopy identified peritoneal micrometastases that had been undetected by stereomicroscopy. Micrometastases as small as a single cell are detectable in this model. This peritoneal micrometastatic model should be a useful tool for research on metastasis of gastric cancer.
为建立一个可见的腹膜微转移模型,将表达增强型绿色荧光蛋白(EGFP)的质粒载体转染至胃癌细胞系MKN-45。将高表达EGFP的细胞注射到裸鼠的腹腔内。然后,在第1、4和7天收获腹膜和腹部器官并进行观察。荧光立体显微镜可识别出立体显微镜未检测到的腹膜微转移灶。在该模型中可检测到小至单个细胞的微转移灶。这个腹膜微转移模型应该是研究胃癌转移的一个有用工具。