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ASH2L蛋白的低表达与急性髓系白血病的良好预后相关。

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

作者信息

Butler Jill S, Qiu Yi Hua, Zhang Nianxiang, Yoo Suk-Young, Coombes Kevin R, Dent Sharon Y R, Kornblau Steven M

机构信息

a Department of Epigenetics and Molecular Carcinogenesis , The University of Texas MD Anderson Cancer Center , Science Park , Smithville , TX , USA.

b Center for Cancer Epigenetics, The University of Texas MD Anderson Cancer Center , Houston , TX , USA.

出版信息

Leuk Lymphoma. 2017 May;58(5):1207-1218. doi: 10.1080/10428194.2016.1235272. Epub 2016 Oct 13.

Abstract

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 (RPPA) technology. We discovered that ASH2L expression is significantly increased in a subset of patients carrying fms-related tyrosine kinase 3 (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.

摘要

ASH2L编码一种三体组蛋白,它是所有已鉴定的哺乳动物组蛋白H3K4甲基转移酶复合物的核心成分,包括混合谱系白血病(MLL)复合物。原发性白血病患者样本中的ASH2L蛋白水平尚未明确。我们使用反相蛋白质阵列(RPPA)技术分析了511例原发性AML患者样本中的ASH2L蛋白表达。我们发现,在携带fms相关酪氨酸激酶3(FLT3)突变的一部分患者中,ASH2L表达显著增加。此外,我们观察到ASH2L水平较低与总生存期延长有关。我们还将ASH2L水平与此前在该阵列上分析的230种蛋白质的表达进行了比较。ASH2L表达与32种蛋白质呈负相关,这些蛋白质大多参与细胞黏附和细胞周期抑制,而与50种蛋白质呈正相关,其中许多蛋白质促进细胞增殖。这些结果共同表明,较低水平的ASH2L蛋白对AML患者有益。

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