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本文引用的文献

1
PIM2 inhibition as a rational therapeutic approach in B-cell lymphoma.PIM2 抑制作为 B 细胞淋巴瘤的合理治疗方法。
Blood. 2011 Nov 17;118(20):5517-27. doi: 10.1182/blood-2011-03-344374. Epub 2011 Sep 21.
2
Targeting cap-dependent translation blocks converging survival signals by AKT and PIM kinases in lymphoma.靶向 AKT 和 PIM 激酶依赖性翻译阻断物以阻断淋巴瘤中的存活信号。
J Exp Med. 2011 Aug 29;208(9):1799-807. doi: 10.1084/jem.20110846. Epub 2011 Aug 22.
3
Targeting PIM kinase activity significantly augments the efficacy of cytarabine.靶向PIM激酶活性可显著增强阿糖胞苷的疗效。
Br J Haematol. 2012 Jan;156(1):129-32. doi: 10.1111/j.1365-2141.2011.08792.x. Epub 2011 Jun 21.
4
The direct Myc target Pim3 cooperates with other Pim kinases in supporting viability of Myc-induced B-cell lymphomas.直接的Myc靶点Pim3与其他Pim激酶协同作用,以维持Myc诱导的B细胞淋巴瘤的生存能力。
Oncotarget. 2011 Jun;2(6):448-60. doi: 10.18632/oncotarget.283.
5
Mechanisms of cytotoxicity to Pim kinase inhibitor, SGI-1776, in acute myeloid leukemia.Pim 激酶抑制剂 SGI-1776 对急性髓系白血病细胞的细胞毒性作用机制。
Blood. 2011 Jul 21;118(3):693-702. doi: 10.1182/blood-2010-12-323022. Epub 2011 May 31.
6
The serine/threonine kinase Pim-2 is a novel anti-apoptotic mediator in myeloma cells.丝氨酸/苏氨酸激酶 Pim-2 是骨髓瘤细胞中一种新型的抗凋亡介质。
Leukemia. 2011 Jul;25(7):1182-8. doi: 10.1038/leu.2011.60. Epub 2011 Apr 8.
7
For better or for worse: the role of Pim oncogenes in tumorigenesis.不管结果是好是坏:Pim 癌基因在肿瘤发生中的作用。
Nat Rev Cancer. 2011 Jan;11(1):23-34. doi: 10.1038/nrc2986. Epub 2010 Dec 9.
8
A phase II trial of the oral mTOR inhibitor everolimus in relapsed aggressive lymphoma.一项评估口服 mTOR 抑制剂依维莫司治疗复发性侵袭性淋巴瘤的 II 期临床试验。
Leukemia. 2011 Feb;25(2):341-7. doi: 10.1038/leu.2010.226. Epub 2010 Dec 7.
9
Mantle cell lymphoma: biology, pathogenesis, and the molecular basis of treatment in the genomic era.套细胞淋巴瘤:在基因组时代的生物学、发病机制和治疗的分子基础。
Blood. 2011 Jan 6;117(1):26-38. doi: 10.1182/blood-2010-04-189977. Epub 2010 Oct 12.
10
Mantle cell lymphoma: report of the 2009 Mantle Cell Lymphoma Consortium Workshop.套细胞淋巴瘤:2009 年套细胞淋巴瘤联盟研讨会报告。
Leuk Lymphoma. 2010 Mar;51(3):390-8. doi: 10.3109/10428190903503453.

转录和翻译是套细胞淋巴瘤中 Pim 激酶抑制剂 SGI-1776 的主要靶点。

Transcription and translation are primary targets of Pim kinase inhibitor SGI-1776 in mantle cell lymphoma.

机构信息

Department of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, USA.

出版信息

Blood. 2012 Oct 25;120(17):3491-500. doi: 10.1182/blood-2012-02-412643. Epub 2012 Sep 6.

DOI:10.1182/blood-2012-02-412643
PMID:22955922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3482859/
Abstract

Proviral integration site for Moloney murine leukemia virus (Pim) kinases are serine/threonine/tyrosine kinases and oncoproteins that promote tumor progression. Three isoforms of Pim kinases have been identified and are known to phosphorylate numerous substrates, with regulatory functions in transcription, translation, cell cycle, and survival pathways. These kinases are involved in production, proliferation, and survival of normal B cells and are overexpressed in B-cell malignancies such as mantle cell lymphoma (MCL). SGI-1776 is a small molecule and Pim kinase inhibitor with selectivity for Pim-1. We hypothesize that Pim kinase function can be inhibited by SGI-1776 in MCL and that inhibition of phosphorylation of downstream substrates will disrupt transcriptional, translational, and cell cycle processes and promote cell death. SGI-1776 treatment in 4 MCL cell lines resulted in apoptosis induction. Phosphorylation of transcription (c-Myc) and translation targets (4E-BP1), tested in Jeko-1 and Mino, was declined. Consistent with these data, Mcl-1 and cyclin D1 protein levels were decreased. Importantly, similar to cell line data, MCL primary cells but not normal cells showed similar inhibition of substrate phosphorylation and cytotoxicity from SGI-1776 treatment. Genetic knockdown of Pim-1/Pim-2 affected similar proteins in MCL cell lines. Collectively these data demonstrate Pim kinases as therapeutic targets in MCL.

摘要

前病毒整合位点 Moloney 鼠白血病病毒 (Pim) 激酶是丝氨酸/苏氨酸/酪氨酸激酶和癌蛋白,可促进肿瘤进展。已经鉴定出三种 Pim 激酶同工型,已知它们可磷酸化许多底物,在转录、翻译、细胞周期和存活途径中具有调节功能。这些激酶参与正常 B 细胞的产生、增殖和存活,并且在 B 细胞恶性肿瘤(如套细胞淋巴瘤(MCL))中过度表达。SGI-1776 是一种小分子和 Pim 激酶抑制剂,对 Pim-1 具有选择性。我们假设 SGI-1776 可在 MCL 中抑制 Pim 激酶功能,并且抑制下游底物的磷酸化将破坏转录、翻译和细胞周期过程并促进细胞死亡。在 4 种 MCL 细胞系中进行 SGI-1776 处理导致细胞凋亡诱导。在 Jeko-1 和 Mino 中测试的转录(c-Myc)和翻译靶标(4E-BP1)的磷酸化减少。与这些数据一致,Mcl-1 和细胞周期蛋白 D1 蛋白水平降低。重要的是,与细胞系数据类似,MCL 原代细胞而不是正常细胞显示出对 SGI-1776 处理的底物磷酸化和细胞毒性的相似抑制作用。Pim-1/Pim-2 的基因敲低在 MCL 细胞系中影响类似的蛋白。这些数据共同表明 Pim 激酶是 MCL 的治疗靶点。