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Low expression of ASH2L protein correlates with a favorable outcome in acute myeloid leukemia

机译:ASH2L蛋白的低表达与急性髓细胞白血病的良好预后相关

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摘要

ASH2L encodes a trithorax group protein that is a core component of all characterized mammalian histone H3K4 methyltransferase complexes, including Mixed Lineage Leukemia (MLL) complexes. ASH2L protein levels in primary leukemia patient samples have not yet been defined. We analyzed ASH2L protein expression in 511 primary AML patient samples using reverse phase protein array technology. We discovered that ASH2L expression is significantly increased in a subset of patients carrying FLT3 mutations. Furthermore, we observed that low levels of ASH2L are associated with increased overall survival. We also compared ASH2L levels to the expression of 230 proteins previously analyzed on this array. ASH2L expression was inversely correlated with 32 proteins, mostly involved in cell adhesion and cell cycle inhibition, while a positive correlation was observed for 50 proteins, many of which promote cell proliferation. Together, these results indicate that a lower level of ASH2L protein is beneficial to AML patients.
机译:ASH2L编码一个三胸基蛋白,它是所有特征性哺乳动物组蛋白H3K4甲基转移酶复合物(包括混合谱系白血病(MLL)复合物)的核心成分。尚未确定原发性白血病患者样品中的ASH2L蛋白水平。我们使用反相蛋白阵列技术分析了511例原发性AML患者样品中的ASH2L蛋白表达。我们发现在携带FLT3突变的一部分患者中ASH2L表达显着增加。此外,我们观察到低水平的ASH2L与整体生存期增加有关。我们还将ASH2L水平与之前在此阵列上分析的230种蛋白质的表达进行了比较。 ASH2L的表达与32种蛋白质呈负相关,主要参与细胞粘附和细胞周期抑制,而50种蛋白质呈正相关,其中许多促进细胞增殖。总之,这些结果表明,较低水平的ASH2L蛋白对AML患者有益。

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