cDNA microarray analysis of altered gene expression in Ara-C-treated leukemia cells

被引:15
|
作者
Takagaki, K [1 ]
Katsuma, S [1 ]
Horio, T [1 ]
Kaminishi, Y [1 ]
Hada, Y [1 ]
Tanaka, T [1 ]
Ohgi, T [1 ]
Yano, J [1 ]
机构
[1] Nippon Shinyaku Co Ltd, Res Labs, Tsukuba, Ibaraki 3050003, Japan
关键词
cDNA microarray; Ara-C; erythroid differentiation; chaperone; asparagine synthetase;
D O I
10.1016/j.bbrc.2003.08.009
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
The acute lymphoblastic leukemia cell line CCRF-CEM is sensitive to Ara-C and undergoes apoptosis. In contrast, the chronic myelogenous leukemia (CML) cell line K562 is highly resistant to Ara-C, which causes the cells to differentiate into erythrocytes before undergoing apoptosis. We used cDNA microarrays to monitor the alterations in gene expression in these two cell lines under conditions leading to apoptosis or differentiation. Ara-C-treated CCRF-CEM cells were characterized by a cluster of down-regulated chaperone genes, whereas Ara-C-treated K562 cells were characterized by a cluster of up-regulated hemoglobin genes. In K562 cells, Ara-C treatment induced significant down-regulation of the asparagine synthetase gene, which is involved in resistance to L-asparaginase. Sequential treatment with Ara-C and L-asparaginase had a synergistic effect on the inhibition of K562 cell growth, and combination therapy with these two anticancer agents may prove effective in the treatment of CNIL, which cannot be cured by either drug alone. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:351 / 358
页数:8
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