Huang Ming-Shyan, Wang Tzu-Jou, Liang Chung-Ling, Huang Huey-Mei, Yang I-Chi, Yi-Jan Hua, Hsiao Michael
Department of Internal Medicine, Kaohsiung Medical University, Taiwan.
Clin Exp Metastasis. 2002;19(4):359-68. doi: 10.1023/a:1015562532564.
Lung cancer is the most prevalent malignant tumor in the world. Metastasis of the disease causes death in lung cancer patients. Recent study has shown that multiple cascades of gene defects occur in lung cancer. In this report, we established a novel H1299/EGFP tumor model to determine whether H1299 transfected with the enhanced green fluorescent protein (EGFP) gene in vitro and xenotransplanted into SCID mouse lung would permit the detection of lung cancer micrometastasis in vivo. We demonstrated that EGFP-transduced H1299 cells maintained stable high-level EGFP expressions during their growth in vivo. EGFP fluorescence clearly demarcated the primary seeding place and readily allowed for the visualization of distant micrometastasis and local invasion at the single-cell level. Small metastatic and locally invasive foci, including those immediately adjacent to the tumor's leading invasive edge, were almost undetectable by routine hematoxylin and eosin staining and immunohistochemistry. The GFP tagged lung cancer model is superior for the detection and study of physiologically relevant patterns of lung cancer invasion and metastasis in vivo.
肺癌是全球最常见的恶性肿瘤。该疾病的转移导致肺癌患者死亡。最近的研究表明,肺癌中会发生多个基因缺陷级联反应。在本报告中,我们建立了一种新型的H1299/EGFP肿瘤模型,以确定在体外转染增强型绿色荧光蛋白(EGFP)基因并异种移植到SCID小鼠肺部的H1299是否能够在体内检测到肺癌微转移。我们证明,EGFP转导的H1299细胞在体内生长过程中维持稳定的高水平EGFP表达。EGFP荧光清晰地划定了原发接种部位,并易于在单细胞水平上观察远处微转移和局部侵袭。常规苏木精和伊红染色及免疫组织化学几乎检测不到小的转移灶和局部侵袭灶,包括紧邻肿瘤侵袭前沿的那些病灶。GFP标记的肺癌模型在体内检测和研究肺癌侵袭和转移的生理相关模式方面更具优势。