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PML-RARα and Its Phosphorylation Regulate PML Oligomerization and HIPK2 Stability
被引:15
|作者:
Shima, Yutaka
[1
]
Honma, Yuki
[1
]
Kitabayashi, Issay
[1
]
机构:
[1] Natl Canc Ctr, Div Hematol Malignancy, Chuo Ku, Tokyo 1040045, Japan
关键词:
ACUTE PROMYELOCYTIC LEUKEMIA;
ACUTE MYELOID-LEUKEMIA;
RETINOID-X-RECEPTOR;
T(15-17) TRANSLOCATION;
TRANSCRIPTION FACTORS;
NB4;
CELLS;
ACID;
DIFFERENTIATION;
DOMAINS;
ACTIVATION;
D O I:
10.1158/0008-5472.CAN-12-3814
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
The PML gene is frequently fused to the retinoic acid receptor alpha (RAR alpha) gene in acute promyelocytic leukemia (APL), generating a characteristic PML-RAR alpha oncogenic chimera. PML-RAR alpha disrupts the discrete nuclear speckles termed nuclear bodies, which are formed in PML, suggesting that nuclear body disruption is involved in leukemogenesis. Nuclear body formation that relies upon PML oligomerization and its stabilization of the hypoxia-inducible protein kinase (HIPK)-2 is disrupted by expression of the PML-RAR alpha chimera. Here, we report that disruption of nuclear bodies is also mediated by PML-RAR alpha inhibition of PML oligomerization. PKAmediated phosphorylation of PML-RAR alpha blocked its ability to inhibit PML oligomerization and destabilize HIPK2. Our results establish that both PML oligomerization and HIPK2 stabilization at nuclear bodies are important for APL cell differentiation, offering insights into the basis for the most common prodifferentiation therapies of APL used clinically. (C) 2013 AACR.
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页码:4278 / 4288
页数:11
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