Westmead Institute for Cancer Research, Westmead Millennium Institute, University of Sydney, Sydney, New South Wales, Australia.
Exp Hematol. 2012 Mar;40(3):207-215.e1. doi: 10.1016/j.exphem.2011.11.001. Epub 2011 Nov 17.
Although patients with acute lymphoblastic leukemia (ALL) usually achieve complete remission, disease relapse is common and difficult to treat. Para-NO-aspirin (para-NO-ASA) is a novel drug with demonstrated efficacy against a number of solid tumors and most recently chronic lymphocytic leukemia. In this study, we used ALL cell lines to assess the effects on cell viability by flow cytometry and investigated the mechanism of cell death using chemical inhibitors of key molecules and assessed the effects by flow cytometry, electrophoretic mobility shift assay, Western blotting, and quantitative reverse transcription polymerase chain reaction. Para-NO-ASA induced cell death in the pre-B ALL cell lines in association with increased reactive oxygen species, and suppression of nuclear factor-κB (NF-κB) activity. Chemical inhibitors of NF-κB similarly induced apoptosis in ALL cells, suggesting a role for suppression of NF-κB in para-NO-ASA-induced cell death. Modulation of NF-κB was not via regulation of IκB but potentially through suppression of ROCK1 and loss of reduced glutathione. Our results demonstrate that para-NO-ASA potently induces apoptosis in B-lineage ALL cells via a reactive oxygen species-dependent mechanism that is associated with suppression of NF-κB activity.
虽然急性淋巴细胞白血病 (ALL) 患者通常能达到完全缓解,但疾病复发很常见且难以治疗。对-硝基-阿司匹林 (para-NO-ASA) 是一种新型药物,已被证明对多种实体瘤和最近的慢性淋巴细胞白血病有效。在这项研究中,我们使用 ALL 细胞系通过流式细胞术评估细胞活力的影响,并使用关键分子的化学抑制剂研究细胞死亡的机制,通过流式细胞术、电泳迁移率变动分析、Western blot 和定量逆转录聚合酶链反应进行评估。para-NO-ASA 诱导前 B ALL 细胞系细胞死亡,与活性氧增加和核因子-κB (NF-κB) 活性抑制有关。NF-κB 的化学抑制剂也同样诱导 ALL 细胞凋亡,表明抑制 NF-κB 在 para-NO-ASA 诱导的细胞死亡中起作用。NF-κB 的调节不是通过 IκB 的调节,而是可能通过抑制 ROCK1 和还原型谷胱甘肽的丧失来实现。我们的研究结果表明,para-NO-ASA 通过一种依赖于活性氧的机制,强力诱导 B 细胞系 ALL 细胞凋亡,该机制与 NF-κB 活性抑制有关。