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急性髓细胞白血病中 Nrf2 的核基础水平较高会降低对蛋白酶体抑制剂的敏感性。

High basal nuclear levels of Nrf2 in acute myeloid leukemia reduces sensitivity to proteasome inhibitors.

机构信息

School of Pharmacy, University of East Anglia, Norwich, United Kingdom.

出版信息

Cancer Res. 2011 Mar 1;71(5):1999-2009. doi: 10.1158/0008-5472.CAN-10-3018. Epub 2011 Jan 6.

Abstract

Proteasome inhibitors such as bortezomib exhibit clinical efficacy in multiple myeloma, but studies in acute myeloid leukemia (AML) have been disappointing to date. The apparent failure in AML likely reflects a lack of biological understanding that might clarify applications of proteosome inhibitors in this disease. Here we show that AML cells are considerably less sensitive than control noncancerous cells to bortezomib-induced cytotoxicity, permitting most bortezomib-treated AML cells to survive treatment. We traced reduced bortezomib sensitivity to increased basal levels of nuclear Nrf2, a transcription factor that stimulates protective antioxidant enzymes. Bortezomib stimulates cytotoxicity through accumulation of reactive oxygen species (ROS) but elevated basal levels of nuclear Nrf2 present in AML cells reduced ROS levels, permitting AML cells to survive drug treatment. We further found that the Nrf2 transcriptional repressor Bach1 is rapidly inactivated by bortezomib, allowing rapid induction of Nrf2-regulated cytoprotective and detoxification genes that protect AML cells from bortezomib-induced apoptosis. By contrast, nonmalignant control cells lacked constitutive activation of Nrf2, such that bortezomib-mediated inactivation of Bach1 led to a delay in induction of Nrf2-regulated genes, effectively preventing the manifestation of apoptotic protection that is seen in AML cells. Together, our findings argue that AML might be rendered sensitive to proteasome inhibitors by cotreatment with either an Nrf2-inhibitory or Bach1-inhibitory treatment, rationalizing a targeted therapy against AML.

摘要

蛋白酶体抑制剂,如硼替佐米,在多发性骨髓瘤中表现出临床疗效,但迄今为止,在急性髓系白血病(AML)中的研究结果令人失望。AML 中的明显失败可能反映了缺乏生物学理解,这可能阐明了蛋白酶体抑制剂在这种疾病中的应用。在这里,我们表明 AML 细胞对硼替佐米诱导的细胞毒性的敏感性明显低于对照非癌细胞,从而允许大多数接受硼替佐米治疗的 AML 细胞在治疗后存活。我们追踪到降低硼替佐米敏感性的原因是核 Nrf2 的基础水平升高,Nrf2 是一种刺激保护性抗氧化酶的转录因子。硼替佐米通过积累活性氧物种(ROS)来刺激细胞毒性,但 AML 细胞中存在的核 Nrf2 的基础水平升高会降低 ROS 水平,从而使 AML 细胞能够在药物治疗中存活。我们进一步发现,Nrf2 转录抑制剂 Bach1 被硼替佐米迅速失活,从而迅速诱导 Nrf2 调节的细胞保护和解毒基因,保护 AML 细胞免受硼替佐米诱导的细胞凋亡。相比之下,非恶性对照细胞缺乏 Nrf2 的组成性激活,因此硼替佐米介导的 Bach1 失活导致 Nrf2 调节基因的诱导延迟,有效地阻止了在 AML 细胞中观察到的凋亡保护的表现。总之,我们的研究结果表明,通过与 Nrf2 抑制剂或 Bach1 抑制剂联合治疗,AML 可能对蛋白酶体抑制剂敏感,从而为 AML 的靶向治疗提供了依据。

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