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IKKβ 的致癌突变通过 K63 连接的泛素化诱导的全局变化发挥作用,并导致自分泌刺激。

Oncogenic mutations in IKKβ function through global changes induced by K63-linked ubiquitination and result in autocrine stimulation.

机构信息

Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, California, United States of America.

Université Joseph Fourier Grenoble, Grenoble, France.

出版信息

PLoS One. 2018 Oct 18;13(10):e0206014. doi: 10.1371/journal.pone.0206014. eCollection 2018.

Abstract

Mutations at position K171 in the kinase activation loop of Inhibitor of κB kinase beta (IKKβ) occur in multiple myeloma, spleen marginal zone lymphoma and mantle cell lymphoma. Previously, we demonstrated that these result in constitutive kinase activation and stimulate Signal Transducer and Activator of Transcription 3 (STAT3). This work also identified K147 as a site of K63-linked regulatory ubiquitination required for activation of signaling pathways. We now present a more detailed analysis of ubiquitination sites together with a comprehensive examination of the signaling pathways activated by IKKβ K171E mutants. Downstream activation of STAT3 is dependent upon the activity of: UBE2N, the E2 ubiquitin ligase involved in K63-linked ubiquitination; TAK1 (MAP3K7), or TGFβ Activated Kinase, which forms a complex required for NFκB activation; JAK kinases, involved proximally in the phosphorylation of STAT transcription factors in response to inflammatory cytokines; and gp130, or IL-6 Receptor Subunit Beta which, upon binding IL-6 or other specific cytokines, undergoes homodimerization leading to activation of associated JAKs, resulting in STAT activation. We further demonstrate, using an IL-6-responsive cell line, that IKKβ K171E mutants stimulate the release of IL-6 activity into conditioned media. These results show that IKKβ K171E mutants trigger an autocrine loop in which IL-6 is secreted and binds to the IL-6 receptor complex gp130, resulting in JAK activation. Lastly, by examining the differential abundance of proteins associated with K63-only-ubiquitinated IKKβ K171E, proteomic analysis demonstrates the global activation of proliferative responses. As cancers harboring K171-mutated IKKβ are likely to also exhibit activated STAT3 and p44/42 MAPK (Erk1/2), this suggests the possibility of using MAPK (Erk1/2) and JAK inhibitors, or specific ubiquitination inhibitors. K63-linked ubiquitination occurs in other kinases at sites homologous to K147 in IKKβ, including K578 in BRAF V600E, which serves as an oncogenic driver in melanoma and other cancers.

摘要

在多发性骨髓瘤、脾边缘区淋巴瘤和套细胞淋巴瘤中,IKKβ(抑制剂κB 激酶β)激酶激活环中的位置 K171 发生突变。此前,我们证明这些突变导致组成型激酶激活,并刺激信号转导和转录激活因子 3(STAT3)。这项工作还确定 K147 是 K63 连接的调节性泛素化的位点,对于信号通路的激活是必需的。现在,我们提出了一个更详细的泛素化位点分析,并全面检查了 IKKβ K171E 突变体激活的信号通路。STAT3 的下游激活依赖于以下因素的活性:UBE2N,参与 K63 连接泛素化的 E2 泛素连接酶;TAK1(MAP3K7),或 TGFβ 激活激酶,它形成 NFκB 激活所需的复合物;JAK 激酶,参与炎症细胞因子反应中 STAT 转录因子的磷酸化;和 gp130,或 IL-6 受体亚基β,它在与 IL-6 或其他特定细胞因子结合后,发生同源二聚化,导致相关 JAK 的激活,从而导致 STAT 的激活。我们进一步使用 IL-6 反应性细胞系证明,IKKβ K171E 突变体刺激 IL-6 活性释放到条件培养基中。这些结果表明,IKKβ K171E 突变体触发了自分泌环,其中 IL-6 被分泌并与 IL-6 受体复合物 gp130 结合,导致 JAK 的激活。最后,通过检查与 K63 单泛素化的 IKKβ K171E 相关的蛋白质的差异丰度,蛋白质组学分析表明增殖反应的全面激活。由于携带 K171 突变的 IKKβ 的癌症可能也表现出激活的 STAT3 和 p44/42 MAPK(Erk1/2),这表明使用 MAPK(Erk1/2)和 JAK 抑制剂,或特定的泛素化抑制剂的可能性。K63 连接的泛素化发生在 IKKβ 中与 K147 同源的其他激酶中,包括 BRAF V600E 中的 K578,它在黑色素瘤和其他癌症中充当致癌驱动基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5bd/6193727/ef784d4ed6c3/pone.0206014.g001.jpg

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