Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Mol Cancer Res. 2013 May;11(5):494-505. doi: 10.1158/1541-7786.MCR-12-0528. Epub 2013 Feb 5.
Glioblastoma tumors are characterized by their invasiveness and resistance to therapies. The transcription factor signal transducer and activator of transcription 3 (STAT3) was recently identified as a master transcriptional regulator in the mesenchymal subtype of glioblastoma (GBM), which has generated an increased interest in targeting STAT3. We have evaluated more closely the mechanism of action of one particular STAT3 inhibitor, JSI-124 (cucurbitacin I). In this study, we confirmed that JSI-124 inhibits both constitutive and stimulus-induced Janus kinase 2 (JAK2) and STAT3 phosphorylation, and decreases cell proliferation while inducing apoptosis in cultured GBM cells. However, we discovered that before the inhibition of STAT3, JSI-124 activates the nuclear factor-κB (NF-κB) pathway, via NF-κB p65 phosphorylation and nuclear translocation. In addition, JSI-124 treatment induces the expression of IL-6, IL-8, and suppressor of cytokine signaling (SOCS3) mRNA, which leads to a corresponding increase in IL-6, IL-8, and SOCS3 protein expression. Moreover, the NF-κB-driven SOCS3 expression acts as a negative regulator of STAT3, abrogating any subsequent STAT3 activation and provides a mechanism of STAT3 inhibition after JSI-124 treatment. Chromatin immunoprecipitation analysis confirms that NF-κB p65 in addition to other activating cofactors are found at the promoters of IL-6, IL-8, and SOCS3 after JSI-124 treatment. Using pharmacological inhibition of NF-κB and inducible knockdown of NF-κB p65, we found that JSI-124-induced expression of IL-6, IL-8, and SOCS3 was significantly inhibited, showing an NF-κB-dependent mechanism. Our data indicate that although JSI-124 may show potential antitumor effects through inhibition of STAT3, other off-target proinflammatory pathways are activated, emphasizing that more careful and thorough preclinical investigations must be implemented to prevent potential harmful effects.
胶质母细胞瘤肿瘤的特征是其侵袭性和对治疗的耐药性。转录因子信号转导子和转录激活子 3(STAT3)最近被鉴定为胶质母细胞瘤(GBM)间质亚型的主要转录调节因子,这引起了人们对靶向 STAT3 的极大兴趣。我们更仔细地评估了一种特定的 STAT3 抑制剂 JSI-124(葫芦素 I)的作用机制。在这项研究中,我们证实 JSI-124 抑制组成型和刺激诱导的 Janus 激酶 2(JAK2)和 STAT3 磷酸化,并在培养的 GBM 细胞中抑制细胞增殖,同时诱导细胞凋亡。然而,我们发现,在 STAT3 抑制之前,JSI-124 通过 NF-κB p65 磷酸化和核易位激活核因子-κB(NF-κB)途径。此外,JSI-124 处理诱导 IL-6、IL-8 和细胞因子信号转导抑制物(SOCS3)mRNA 的表达,导致 IL-6、IL-8 和 SOCS3 蛋白表达相应增加。此外,NF-κB 驱动的 SOCS3 表达作为 STAT3 的负调节剂,消除任何随后的 STAT3 激活,并为 JSI-124 处理后 STAT3 抑制提供机制。染色质免疫沉淀分析证实,NF-κB p65 以及其他激活共因子,在 JSI-124 处理后,除了其他激活共因子外,还存在于 IL-6、IL-8 和 SOCS3 的启动子中。通过 NF-κB 的药理学抑制和 NF-κB p65 的诱导性敲低,我们发现 JSI-124 诱导的 IL-6、IL-8 和 SOCS3 的表达明显受到抑制,显示出 NF-κB 依赖性机制。我们的数据表明,尽管 JSI-124 可能通过抑制 STAT3 显示出潜在的抗肿瘤作用,但其他非靶向性促炎途径被激活,这强调必须进行更仔细和彻底的临床前研究,以防止潜在的有害影响。