Suryani Santi, Bracken Lauryn S, Harvey Richard C, Sia Keith C S, Carol Hernan, Chen I-Ming, Evans Kathryn, Dietrich Philipp A, Roberts Kathryn G, Kurmasheva Raushan T, Billups Catherine A, Mullighan Charles G, Willman Cheryl L, Loh Mignon L, Hunger Stephen P, Houghton Peter J, Smith Malcolm A, Lock Richard B
Children's Cancer Institute Australia for Medical Research, Lowy Cancer Research Centre, University of New South Wales, Sydney, Australia.
Cancer Center, University of New Mexico, Albuquerque, New Mexico.
Mol Cancer Ther. 2015 Feb;14(2):364-74. doi: 10.1158/1535-7163.MCT-14-0647. Epub 2014 Dec 10.
Genome-wide studies have identified a high-risk subgroup of pediatric acute lymphoblastic leukemia (ALL) harboring mutations in the Janus kinases (JAK). The purpose of this study was to assess the preclinical efficacy of the JAK1/2 inhibitor AZD1480, both as a single agent and in combination with the MEK inhibitor selumetinib, against JAK-mutated patient-derived xenografts. Patient-derived xenografts were established in immunodeficient mice from bone marrow or peripheral blood biopsy specimens, and their gene expression profiles compared with the original patient biopsies by microarray analysis. JAK/STAT and MAPK signaling pathways, and the inhibitory effects of targeted drugs, were interrogated by immunoblotting of phosphoproteins. The antileukemic effects of AZD1480 and selumetinib, alone and in combination, were tested against JAK-mutated ALL xenografts both in vitro and in vivo. Xenografts accurately represented the primary disease as determined by gene expression profiling. Cellular phosphoprotein analysis demonstrated that JAK-mutated xenografts exhibited heightened activation status of JAK/STAT and MAPK signaling pathways compared with typical B-cell precursor ALL xenografts, which were inhibited by AZD1480 exposure. However, AZD1480 exhibited modest single-agent in vivo efficacy against JAK-mutated xenografts. Combining AZD1480 with selumetinib resulted in profound synergistic in vitro cell killing, although these results were not translated in vivo despite evidence of target inhibition. Despite validation of target inhibition and the demonstration of profound in vitro synergy between AZD1480 and selumetinib, it is likely that prolonged target inhibition is required to achieve in vivo therapeutic enhancement between JAK and MEK inhibitors in the treatment of JAK-mutated ALL.
全基因组研究已确定了小儿急性淋巴细胞白血病(ALL)的一个高危亚组,其携带Janus激酶(JAK)突变。本研究的目的是评估JAK1/2抑制剂AZD1480作为单一药物以及与MEK抑制剂司美替尼联合使用时,对携带JAK突变的患者来源异种移植瘤的临床前疗效。从骨髓或外周血活检标本中在免疫缺陷小鼠体内建立患者来源的异种移植瘤,并通过微阵列分析将其基因表达谱与原始患者活检标本进行比较。通过磷酸化蛋白的免疫印迹法研究JAK/STAT和MAPK信号通路以及靶向药物的抑制作用。在体外和体内测试了AZD1480和司美替尼单独及联合使用对携带JAK突变的ALL异种移植瘤的抗白血病作用。通过基因表达谱分析确定,异种移植瘤准确代表了原发性疾病。细胞磷酸化蛋白分析表明,与典型的B细胞前体ALL异种移植瘤相比,携带JAK突变的异种移植瘤表现出JAK/STAT和MAPK信号通路更高的激活状态,而AZD1480暴露可抑制这些通路。然而,AZD1480对携带JAK突变的异种移植瘤的单药体内疗效一般。将AZD1480与司美替尼联合使用可导致体外细胞杀伤作用产生显著协同效应,尽管有靶点抑制的证据,但这些结果在体内并未转化。尽管验证了靶点抑制以及AZD1480和司美替尼之间在体外具有显著协同作用,但在治疗携带JAK突变的ALL时,可能需要延长靶点抑制时间才能实现JAK和MEK抑制剂之间的体内治疗增强效果。