INDUCTION OF APOPTOSIS BY A DOMINANT-NEGATIVE H-RAS MUTANT (116Y) IN K562 CELLS

被引:50
作者
SAKAI, N
OGISO, Y
FUJITA, H
WATARI, H
KOIKE, T
KUZUMAKI, N
机构
[1] HOKKAIDO UNIV,SCH MED,INST CANC,MOLEC GENET LAB,SAPPORO,HOKKAIDO 060,JAPAN
[2] HOKKAIDO UNIV,SCH MED,DEPT INTERNAL MED 2,SAPPORO,HOKKAIDO 060,JAPAN
关键词
D O I
10.1006/excr.1994.1324
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent extensive work on apoptosis has begun to reveal its molecular mechanisms. Several genes that regulate apoptosis have been identified. Among them, the BCL2 gene is considered to be an important gene that inhibits apoptosis. However, there must be other genes, yet to be identified, which suppress apoptosis. It has been suggested that the activation of RAS function by BCR-ABL fusion protein in chronic myelogenous leukemia may be an important mechanism in the BCR-ABL mediated transformation. Therefore, in this study we have investigated whether the suppression of endogenous H-RAS function inhibits the BCR-ABL mediated transforming activity in a K562 human chronic myelogenous leukemia cell line. The induced expression of a dominant negative v-H-RAS mutant (116Y) in K562 cells has resulted in cell death. The morphological characteristics and the detection of fragmented DNA by gel electrophoresis in the dead cells have revealed that this cell death is apoptosis. These results directly indicate that the RAS gene as well as the BCL2 gene has an ability to suppress apoptosis. (C) 1994 Academic Press, Inc.
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页码:131 / 136
页数:6
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