Kim Sung-Hye, Seo Hee-Won, Lee Min-Ho, Chung Jin-Ho, Lee Byung Hoon, Lee Mi-Ock
14College of Pharmacy, Seoul National University, Seoul, 151-742 Korea.
24Bio-MAX Institute, Seoul National University, Seoul, 151-742 Korea.
Toxicol Res. 2009 Dec;25(4):189-193. doi: 10.5487/TR.2009.25.4.189. Epub 2009 Dec 30.
Hypoxia inducible factor 1α (HIF-1α) is a potential marker of carcicnogenesis since it is overexpresssed in many human cancers such as brain, breast, and uterus, and its role has implicated in tumor cell growth and metastasis. In this study, we established a stable cell line that express green fluorescence protein (GFP)-fused hypoxia inducible factor 1α (HIF-1α) and evaluated the potential use of this cell line for assessment of carcinogenicity of chemical toxicants. Western blot analysis as well as fluorescence measurements showed that protein-level of GFP-HIF-1α was significantly enhanced in a dose-dependent manner upon treatment of hypoxia mimicking agents such as dexferrioxamine and CoCl. Well-Known tumor promoters such as mitomycin and methyl methane-sulfonate. significantly induced the fluorescence intensity of GFP-HIF-1α, whereas the known negative controls such as -anthranilic acid and benzethonium chloride, did not. These results indicate that HIF-1α could be a biological parameter for detection of tumor initiators/promoters and suggest that the GFP-HIF-1α cell line is a useful system for screening of carcinogenic toxicants.
缺氧诱导因子1α(HIF-1α)是一种潜在的致癌标志物,因为它在许多人类癌症中过度表达,如脑癌、乳腺癌和子宫癌,并且其作用与肿瘤细胞的生长和转移有关。在本研究中,我们建立了一种稳定表达绿色荧光蛋白(GFP)融合缺氧诱导因子1α(HIF-1α)的细胞系,并评估了该细胞系在评估化学毒物致癌性方面的潜在用途。蛋白质印迹分析以及荧光测量表明,在用去铁胺和氯化钴等模拟缺氧剂处理后,GFP-HIF-1α的蛋白质水平以剂量依赖的方式显著增强。丝裂霉素和甲磺酸甲酯等著名的肿瘤启动子显著诱导了GFP-HIF-1α的荧光强度,而邻氨基苯甲酸和苄索氯铵等已知的阴性对照则没有。这些结果表明,HIF-1α可能是检测肿瘤启动剂/促进剂的生物学参数,并表明GFP-HIF-1α细胞系是筛选致癌毒物的有用系统。