Ral promotes anchorage-independent growth of a human fibrosarcoma, HT1080

被引:13
作者
Yamazaki, Y [1 ]
Kaziro, Y [1 ]
Koide, H [1 ]
机构
[1] Tokyo Inst Technol, Fac Biosci & Biotechnol, Midori Ku, Yokohama, Kanagawa 2268501, Japan
关键词
ral; ras; p27(Kip1); anchorage-independent growth; HT1080;
D O I
10.1006/bbrc.2000.4233
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ral has been shown to act downstream of Ras oncoprotein. However, the role of Ral in Has-induced cellular transformation has not been fully understood. To test the involvement of Ral in Has-induced anchorage-independent growth, we ectopically expressed Ral mutants in HT1080 cells, whose ability to grow in the absence of anchorage depends on the oncogenic mutation of N-ras. Expression of an activated mutant of Ral resulted in enhanced growth of HT1080 cells in soft agar, whereas a dominant-negative mutant of Ral inhibited their anchorage-independent growth. Moreover, the activated Ral mutant decreased the amount of p27(Kip1) in the absence of adhesion, while the dominant-negative mutant increased it. These results suggest that Ral is involved in the Ras-dependent anchorage-independent growth of HT1080 cells by regulating p27(Kip1). (C) 2001 Academic Press.
引用
收藏
页码:868 / 873
页数:6
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