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Node-negative colorectal cancer at high risk of distant metastasis identified by combined analysis of lymph node status, vascular invasion, and Raf-1 kinase inhibitor protein expression.通过淋巴结状态、血管侵犯和Raf-1激酶抑制蛋白表达的联合分析确定的具有远处转移高风险的淋巴结阴性结直肠癌
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FoxM1 regulates growth factor-induced expression of kinase-interacting stathmin (KIS) to promote cell cycle progression.FoxM1调节生长因子诱导的激酶相互作用的微管相关蛋白(KIS)表达,以促进细胞周期进程。
J Biol Chem. 2008 Jan 4;283(1):453-460. doi: 10.1074/jbc.M705792200. Epub 2007 Nov 5.
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RKIP does not contribute to MAP kinase pathway silencing in the Merkel Cell Carcinoma cell line UISO.在默克尔细胞癌细胞系UISO中,RKIP对丝裂原活化蛋白激酶(MAP)信号通路的沉默没有作用。
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Targeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancer.靶向Raf-MEK-ERK丝裂原活化蛋白激酶级联反应用于癌症治疗。
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Hyperactive Ras in developmental disorders and cancer.发育障碍和癌症中过度活跃的Ras
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Growth-suppressive function of phosphatidylethanolamine-binding protein in anaplastic thyroid cancer.
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Raf kinase inhibitor protein expression in a survival analysis of colorectal cancer patients.Raf激酶抑制蛋白在结直肠癌患者生存分析中的表达
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The G protein-coupled receptor kinase (GRK) interactome: role of GRKs in GPCR regulation and signaling.G蛋白偶联受体激酶(GRK)相互作用组:GRKs在GPCR调节和信号传导中的作用
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Bcr-Abl 导致 Raf 激酶抑制剂蛋白表达减少,进而促进慢性髓性白血病的增殖。

Reduction of Raf kinase inhibitor protein expression by Bcr-Abl contributes to chronic myelogenous leukemia proliferation.

机构信息

Department of Internal Medicine III, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-ku, Hamamatsu, Shizuoka 431-3192, Japan.

出版信息

J Biol Chem. 2010 Feb 26;285(9):6585-94. doi: 10.1074/jbc.M109.075788. Epub 2009 Dec 22.

DOI:10.1074/jbc.M109.075788
PMID:20028985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2825454/
Abstract

Chronic myelogenous leukemia (CML) is characterized by a reciprocal chromosomal translocation (9;22) that generates the Bcr-Abl fusion gene. The Ras/Raf-1/MEK/ERK pathway is constitutively activated in Bcr-Abl-transformed cells, and Ras activity enhances the oncogenic ability of Bcr-Abl. However, the mechanism by which Bcr-Abl activates the Ras pathway is not completely understood. Raf kinase inhibitor protein (RKIP) inhibits activation of MEK by Raf-1 and its downstream signal transduction, resulting in blocking the MAP kinase pathway. In the present study, we found that RKIP was depleted in CML cells. We investigated the interaction between RKIP and Bcr-Abl in CML cell lines and Bcr-Abl(+) progenitor cells from CML patients. The Abl kinase inhibitors and depletion of Bcr-Abl induced the expression of RKIP and reduced the pERK1/2 status, resulting in inhibited proliferation of CML cells. Moreover, RKIP up-regulated cell cycle regulator FoxM1 expression, resulting in G(1) arrest via p27(Kip1) and p21(Cip1) accumulation. In colony-forming unit granulocyte, erythroid, macrophage, megakaryocyte, colony-forming unit-granulocyte macrophage, and burst-forming unit erythroid, treatment with the Abl kinase inhibitors and depletion of Bcr-Abl induced RKIP and reduced FoxM1 expressions, and inhibited colony formation of Bcr-Abl(+) progenitor cells, whereas depletion of RKIP weakened the inhibition of colony formation activity by the Abl kinase inhibitors in Bcr-Abl(+) progenitor cells. Thus, Bcr-Abl represses the expression of RKIP, continuously activates pERK1/2, and suppresses FoxM1 expression, resulting in proliferation of CML cells.

摘要

慢性髓性白血病(CML)的特征是发生一种相互易位(9;22),从而产生 Bcr-Abl 融合基因。Bcr-Abl 转化细胞中 Ras/Raf-1/MEK/ERK 途径持续激活,而 Ras 活性增强了 Bcr-Abl 的致癌能力。然而,Bcr-Abl 激活 Ras 途径的机制尚不完全清楚。Raf 激酶抑制剂蛋白(RKIP)抑制 Raf-1 激活 MEK 及其下游信号转导,从而阻断 MAP 激酶途径。在本研究中,我们发现 CML 细胞中 RKIP 耗竭。我们研究了 CML 细胞系和 CML 患者的 Bcr-Abl(+)祖细胞中 RKIP 与 Bcr-Abl 的相互作用。Abl 激酶抑制剂和 Bcr-Abl 的耗竭诱导了 RKIP 的表达,并降低了 pERK1/2 状态,导致 CML 细胞增殖受到抑制。此外,RKIP 上调了细胞周期调节因子 FoxM1 的表达,通过 p27(Kip1)和 p21(Cip1)的积累导致 G1 期停滞。在集落形成单位粒细胞、红细胞、巨噬细胞、巨核细胞、粒细胞巨噬细胞集落形成单位和红细胞爆式集落形成单位中,Abl 激酶抑制剂处理和 Bcr-Abl 的耗竭诱导 RKIP 的表达,并降低 FoxM1 的表达,抑制 Bcr-Abl(+)祖细胞的集落形成,而 RKIP 的耗竭削弱了 Abl 激酶抑制剂在 Bcr-Abl(+)祖细胞中对集落形成活性的抑制作用。因此,Bcr-Abl 抑制 RKIP 的表达,持续激活 pERK1/2,并抑制 FoxM1 的表达,导致 CML 细胞的增殖。