ASB-2 inhibits growth and promotes commitment in myeloid leukemia cells

被引:78
作者
Guibal, FC
Moog-Lutz, C
Smolewski, P
Di Gioia, Y
Darzynkiewicz, Z
Lutz, PG
Cayre, YE
机构
[1] Hop St Antoine, Unite INSERM U417, F-75012 Paris, France
[2] New York Med Coll, Brander Canc Res Inst, Hawthorne, NY 10532 USA
[3] Thomas Jefferson Univ, Kimmel Canc Inst, Dept Immunol Microbiol, Philadelphia, PA 19107 USA
关键词
D O I
10.1074/jbc.M108476200
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
In acute promyelocytic leukemia (APL) cells harboring the promyelocytic leukemia retinoic acid receptor alpha (PML-RARalpha) chimeric protein, retinoic acid (RA)-induced differentiation is triggered through a PML-RARa signaling resulting in activation of critical target genes. Induced differentiation of APL cells is always preceded by withdrawal from the cell cycle and commitment events leading to terminal differentiation. Here we have identified the human ankyrin repeat-containing protein with a suppressor of cytokine signaling box-2 (ASB-2) cDNA, as a novel RA-induced gene in APL cells. PML/RARalpha strongly enhanced RA-induced ASB-2 mRNA expression. In myeloid leukemia cells, ASB-2 expression induced growth inhibition and chromatin condensation recapitulating early events critical to RA-induced differentiation of APL cells.
引用
收藏
页码:218 / 224
页数:7
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