Laterra J, Rosen E, Nam M, Ranganathan S, Fielding K, Johnston P
Department of Neurology, The Johns Hopkins University School of Medicine, The Kennedy Krieger Research Institute, Baltimore, Maryland 21205, USA.
Biochem Biophys Res Commun. 1997 Jun 27;235(3):743-7. doi: 10.1006/bbrc.1997.6853.
We have shown previously that the multifunctional cytokine scatter factor/hepatocyte growth factor (SF/HGF) is elevated in human malignant gliomas. In this study we investigated how human SF/HGF expression affects the malignancy of the U373 human glioblastoma cell line in vivo and in vitro. Human SF/HGF gene transfer increased U373 glioblastoma tumorigenicity by > or = 20-fold and enhanced the growth rate of intracerebral U373 xenografts by 3- to 8-fold. SF/HGF expression had no effect on the proliferation of glioblastoma cell monolayers but increased their anchorage-independent colony formation in soft agar by 5- to 8-fold. These results are the first to show that SF/HGF expression by human glioblastoma cells enhances their growth dysregulation in vitro and malignancy in vivo.
我们先前已表明,多功能细胞因子分散因子/肝细胞生长因子(SF/HGF)在人类恶性胶质瘤中升高。在本研究中,我们调查了人类SF/HGF表达如何在体内和体外影响U373人胶质母细胞瘤细胞系的恶性程度。人类SF/HGF基因转移使U373胶质母细胞瘤的致瘤性增加了20倍或更多,并使脑内U373异种移植物的生长速率提高了3至8倍。SF/HGF表达对胶质母细胞瘤细胞单层的增殖没有影响,但使它们在软琼脂中不依赖贴壁的集落形成增加了5至8倍。这些结果首次表明,人胶质母细胞瘤细胞表达SF/HGF会增强其在体外的生长失调和在体内的恶性程度。