The roles of phosphorylation of signaling proteins in the prognosis of acute myeloid leukemia

Adrienn Márton, Katalin Beáta Veres, F. Erdődi, Miklós Udvardy, Árpád Illés, László Rejtő
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Abstract

Signaling pathways of Retinoblastoma (Rb) protein, Akt-kinase, and Erk-kinase (extracellular signal-regulated kinase) have an important role in the pathogenesis of acute myeloid leukemia. Constitutive activation of these proteins by phosphorylation contributes to cell survival by regulation of cell cycle, proliferation and proapoptotic signaling processes. According to previous data phosphorylated forms of these proteins represent a worse outcome for cancer patients. We investigated the presence of phosphorylated Rb (P-Rb), Akt (P-Akt) and Erk (P-Erk) proteins by Western blot technique using phospho-specific antibodies in bone marrow or peripheral blood samples of 69 AML patients, 36 patients with myelodysplastic syndrome (MDS) and 10 healthy volunteers. Expression level of PTEN (Phosphatase and tensin homolog) and PHLPP (PH domain and leucine-rich repeat Protein Phosphatase) phosphatases, the negative regulators of Akt kinase pathway were also examined. We tested the effect of these proteins on survival and on the correlation with known prognostic features in AML. We found 46.3% of AML patients had detectable P-Rb, 34.7% had P-Akt and 28.9% had P-Erk protein. 66.1% of patients expressing PTEN, 38.9% PHLPP, 37.2% both PTEN and PHLPP and 32.2% neither PTEN nor PHLPP phosphatases. Compared to nucleophosmin mutation (NPMc) negative samples P-Erk was significantly less in nucleophosmin mutated patients, P-Rb was significantly less in patients’ group with more than 30 G/L peripheral leukocyte count by diagnosis. PHLPP was significantly present in FAB type M5. The expression of P-Rb represented significant better overall survival (OS), while P-Akt represented significantly worse event-free survival (EFS) in unfavorable cytogenetics patients. The presence of both PHLPP and PTEN phosphatases contributes to better OS and EFS, although the differences were not statistically significant. We confirmed significant positive correlation between P-Akt and PHLPP. Assessing the phosphorylation of Rb, Akt and Erk may define a subgroup of AML patients who would benefit especially from new targeted treatment options complemented the standard chemotherapy, and it may contribute to monitoring remission, relapse or progression of AML.
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信号蛋白磷酸化在急性髓性白血病预后中的作用
视网膜母细胞瘤(Rb)蛋白、Akt 激酶和 Erk 激酶(细胞外信号调节激酶)的信号通路在急性髓性白血病的发病机制中起着重要作用。这些蛋白通过磷酸化被持续激活,通过调节细胞周期、增殖和促凋亡信号转导过程促进细胞存活。根据以往的数据,这些蛋白的磷酸化形式意味着癌症患者的预后较差。我们使用磷酸化特异性抗体,通过 Western 印迹技术检测了 69 名 AML 患者、36 名骨髓增生异常综合征(MDS)患者和 10 名健康志愿者骨髓或外周血样本中磷酸化 Rb(P-Rb)、Akt(P-Akt)和 Erk(P-Erk)蛋白的存在情况。我们还检测了 Akt 激酶通路的负调控因子 PTEN(磷酸酶和天丝同源物)和 PHLPP(PH 结构域和富亮氨酸重复蛋白磷酸酶)磷酸酶的表达水平。我们检测了这些蛋白对存活率的影响以及与急性髓细胞性白血病已知预后特征的相关性。我们发现46.3%的急性髓细胞性白血病患者检测到P-Rb蛋白,34.7%检测到P-Akt蛋白,28.9%检测到P-Erk蛋白。66.1%的患者表达PTEN,38.9%表达PHLPP,37.2%同时表达PTEN和PHLPP,32.2%既不表达PTEN也不表达PHLPP磷酸酶。与核嗜酸基因突变(NPMc)阴性样本相比,核嗜酸基因突变患者中的P-Erk明显较少,P-Rb在诊断时外周血白细胞计数超过30 G/L的患者组中明显较少。PHLPP在FAB M5型中明显存在。在不利细胞遗传学患者中,P-Rb的表达明显提高了总生存率(OS),而P-Akt的表达则明显降低了无事件生存率(EFS)。PHLPP和PTEN磷酸酶的存在有助于提高OS和EFS,尽管差异在统计学上并不显著。我们证实,P-Akt与PHLPP之间存在明显的正相关性。对Rb、Akt和Erk的磷酸化进行评估,可以确定急性髓细胞性白血病患者的一个亚组,这些患者将特别受益于新的靶向治疗方案和标准化疗的补充,而且还有助于监测急性髓细胞性白血病的缓解、复发或进展。
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