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PML-RARα 及其磷酸化调节 PML 寡聚化和 HIPK2 稳定性。

PML-RARα and its phosphorylation regulate pml oligomerization and HIPK2 stability.

机构信息

Division of Hematological Malignancy, National Cancer Center Research Institute, Chuo-ku, Tokyo, Japan.

出版信息

Cancer Res. 2013 Jul 15;73(14):4278-88. doi: 10.1158/0008-5472.CAN-12-3814. Epub 2013 May 30.

Abstract

The PML gene is frequently fused to the retinoic acid receptor α (RARα) gene in acute promyelocytic leukemia (APL), generating a characteristic PML-RARα oncogenic chimera. PML-RARα 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-RARα chimera. Here, we report that disruption of nuclear bodies is also mediated by PML-RARα inhibition of PML oligomerization. PKA-mediated phosphorylation of PML-RARα 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.

摘要

早幼粒细胞白血病(APL)中,PML 基因常与维甲酸受体 α(RARα)基因融合,产生特征性的 PML-RARα致癌嵌合体。PML-RARα破坏了离散的核斑点,称为核体,这是在 PML 中形成的,表明核体破坏参与了白血病的发生。依赖于 PML 寡聚化及其稳定缺氧诱导蛋白激酶(HIPK)-2 的核体形成,被 PML-RARα嵌合体的表达破坏。在这里,我们报告说,核体的破坏也被 PML-RARα抑制 PML 寡聚化所介导。PKA 介导的 PML-RARα磷酸化阻断了其抑制 PML 寡聚化和不稳定 HIPK2 的能力。我们的结果确立了核体中 PML 寡聚化和 HIPK2 的稳定对于 APL 细胞分化都是重要的,为临床上最常用的 APL 促分化治疗的基础提供了深入了解。

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