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Gadd45a基因缺陷会加速BCR-ABL驱动的慢性粒细胞白血病进程。

Gadd45a deficiency accelerates BCR-ABL driven chronic myelogenous leukemia.

作者信息

Mukherjee Kaushiki, Sha Xiaojin, Magimaidas Andrew, Maifrede Silvia, Skorski Tomasz, Bhatia Ravi, Hoffman Barbara, Liebermann Dan A

机构信息

Fels Institute for Cancer Research and Molecular Biology, Philadelphia, PA, USA.

Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Oncotarget. 2017 Feb 14;8(7):10809-10821. doi: 10.18632/oncotarget.14580.

Abstract

The Gadd45a stress sensor gene is a member in the Gadd45 family of genes that includes Gadd45b & Gadd45g. To investigate the effect of GADD45A in the development of CML, syngeneic wild type lethally irradiated mice were reconstituted with either wild type or Gadd45a null myeloid progenitors transduced with a retroviral vector expressing the 210-kD BCR-ABL fusion oncoprotein. Loss of Gadd45a was observed to accelerate BCR-ABL driven CML resulting in the development of a more aggressive disease, a significantly shortened median mice survival time, and increased BCR-ABL expressing leukemic stem/progenitor cells (GFP+Lin- cKit+Sca+). GADD45A deficient progenitors expressing BCR-ABL exhibited increased proliferation and decreased apoptosis relative to WT counterparts, which was associated with enhanced PI3K-AKT-mTOR-4E-BP1 signaling, upregulation of p30C/EBPα expression, and hyper-activation of p38 and Stat5. Furthermore, Gadd45a expression in samples obtained from CML patients was upregulated in more indolent chronic phase CML samples and down regulated in aggressive accelerated phase CML and blast crisis CML. These results provide novel evidence that Gadd45a functions as a suppressor of BCR/ABL driven leukemia and may provide a unique prognostic marker of CML progression.

摘要

Gadd45a应激传感器基因是Gadd45基因家族的成员之一,该家族还包括Gadd45b和Gadd45g。为了研究GADD45A在慢性粒细胞白血病(CML)发展中的作用,用表达210-kD BCR-ABL融合癌蛋白的逆转录病毒载体转导野生型或Gadd45a基因缺失的同基因骨髓祖细胞,对经致死剂量照射的野生型小鼠进行重建。结果发现,Gadd45a缺失会加速BCR-ABL驱动的CML发展,导致病情更具侵袭性、小鼠中位生存时间显著缩短,以及表达BCR-ABL的白血病干/祖细胞(GFP+Lin-cKit+Sca+)增加。与野生型对应物相比,表达BCR-ABL的GADD45A缺陷祖细胞增殖增加、凋亡减少,这与PI3K-AKT-mTOR-4E-BP1信号增强、p30C/EBPα表达上调以及p38和Stat5过度激活有关。此外,从CML患者获得的样本中,Gadd45a的表达在病情较缓和的慢性期CML样本中上调,而在侵袭性加速期CML和急变期CML中下调。这些结果提供了新的证据,表明Gadd45a作为BCR/ABL驱动的白血病的抑制因子发挥作用,并可能为CML进展提供独特的预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f26c/5355225/3ca4d5ef77d9/oncotarget-08-10809-g001.jpg

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