Sassano Antonella, Lo Iacono Marco, Antico Giovanni, Jordan Alison, Uddin Shahab, Calogero Raffaele A, Platanias Leonidas C
Robert H. Lurie Comprehensive Cancer Center, Northwestern University Medical School, 303 East Superior Street, Lurie 3-107, Chicago, IL 60611, USA.
Mol Cancer Ther. 2009 Mar;8(3):615-25. doi: 10.1158/1535-7163.MCT-08-1196. Epub 2009 Feb 24.
There is emerging evidence that, beyond their cholesterol-lowering properties, statins exhibit important antileukemic effects in vitro and in vivo, but the precise mechanisms by which they generate such responses remain to be determined. We have previously shown that statins promote differentiation of acute promyelocytic leukemia cells and enhance generation of all-trans retinoic acid (ATRA)-dependent antileukemic responses. We now provide evidence that statin-dependent leukemic cell differentiation requires engagement and activation of the c-Jun NH2-terminal kinase kinase pathway. In addition, in experiments, to define the molecular targets and mediators of statin-induced differentiation, we found a remarkable effect of statins on ATRA-dependent gene transcription, evidenced by the selective induction of over 400 genes by the combination of atorvastatin and ATRA. Altogether, our studies identify novel statin molecular targets linked to differentiation, establish that statins modulate ATRA-dependent transcription, and suggest that combined use of statins with retinoids may provide a novel approach to enhance antileukemic responses in acute promyelocytic leukemia and possibly other leukemias.
越来越多的证据表明,他汀类药物除了具有降胆固醇特性外,在体外和体内还表现出重要的抗白血病作用,但其产生这些反应的确切机制仍有待确定。我们之前已经表明,他汀类药物可促进急性早幼粒细胞白血病细胞的分化,并增强全反式维甲酸(ATRA)依赖性抗白血病反应的产生。我们现在提供证据表明,他汀类药物依赖性白血病细胞分化需要c-Jun氨基末端激酶激酶途径的参与和激活。此外,在实验中,为了确定他汀类药物诱导分化的分子靶点和介质,我们发现他汀类药物对ATRA依赖性基因转录有显著影响,阿托伐他汀和ATRA联合使用可选择性诱导400多个基因,这证明了这一点。总之,我们的研究确定了与分化相关的新型他汀类药物分子靶点,证实他汀类药物可调节ATRA依赖性转录,并表明他汀类药物与维甲酸联合使用可能为增强急性早幼粒细胞白血病以及可能其他白血病的抗白血病反应提供一种新方法。