Lalic Hrvoje, Dembitz Vilma, Lukinovic-Skudar Vesna, Banfic Hrvoje, Visnjic Dora
Department of Physiology and Croatian Institute for Brain Research, School of Medicine, University of Zagreb , Croatia.
Leuk Lymphoma. 2014 Oct;55(10):2375-83. doi: 10.3109/10428194.2013.876633. Epub 2014 Feb 24.
Adenosine monophosphate (AMP)-activated kinase (AMPK) modulators have been shown to exert cytotoxic activity in hematological malignancies, but their role in the differentiation of acute myeloid leukemia (AML) is less explored. In this study, the effects of AMPK agonists on all-trans retinoic acid (ATRA)-mediated differentiation of acute promyelocytic leukemia (APL) and non-APL AML cell lines were investigated. The results show that AMPK agonists inhibit the growth of myeloblastic HL-60, promyelocytic NB4 and monocytic U937 cells. 5-Aminoimidazole-4-carboxamide ribonucleoside (AICAR), an AMPK activator, enhances ATRA-mediated differentiation of NB4 cells. In U937 cells, AICAR alone induces the expression of cell surface markers associated with mature monocytes and macrophages. In both cell lines, AICAR increases the activity of mitogen-activated protein kinase (MAPK), and the presence of a MAPK inhibitor reduces the expression of differentiation markers. These results reveal beneficial effects of AICAR in AML, including differentiation of non-APL AML cells.
一磷酸腺苷(AMP)激活的蛋白激酶(AMPK)调节剂已被证明在血液系统恶性肿瘤中具有细胞毒活性,但其在急性髓系白血病(AML)分化中的作用尚未得到充分研究。在本研究中,我们调查了AMPK激动剂对全反式维甲酸(ATRA)介导的急性早幼粒细胞白血病(APL)和非APL AML细胞系分化的影响。结果表明,AMPK激动剂可抑制髓母细胞性HL-60、早幼粒细胞性NB4和单核细胞性U937细胞的生长。AMPK激活剂5-氨基咪唑-4-甲酰胺核苷(AICAR)可增强ATRA介导的NB4细胞分化。在U937细胞中,单独使用AICAR可诱导与成熟单核细胞和巨噬细胞相关的细胞表面标志物的表达。在这两种细胞系中,AICAR均可增加丝裂原活化蛋白激酶(MAPK)的活性,而MAPK抑制剂的存在则可降低分化标志物的表达。这些结果揭示了AICAR在AML中的有益作用,包括非APL AML细胞的分化。