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泛素-蛋白酶体途径在皮肤癌发展中的作用:26S 蛋白酶体激活的 NF-κB 信号转导。

The role of the ubiquitin-proteasome pathway in skin cancer development: 26S proteasome-activated NF-κB signal transduction.

机构信息

Laboratory of Biochemistry, Environment and Agri-Food (URAC 36) -Faculty of Sciences and Technology -Mohammedia, Hassan II University, Casablanca, Morocco.

Laboratory of Materials, Membranes, and Environment, Faculty of Science and Technology-Mohammedia, Hassan II University, Casablanca, Morocco.

出版信息

Cancer Biol Ther. 2021 Dec 2;22(10-12):479-492. doi: 10.1080/15384047.2021.1978785. Epub 2021 Sep 29.

Abstract

The Ubiquitin-Proteasome System plays a central role in signal transduction associated with stress, in the skin in particular by the control of NF-κB pathways. Under normal conditions, the inhibitory protein IκB is phosphorylated by kinases, then ubiquitinated and ends up at the proteasome to be degraded. The present short review discusses recent progress in the inhibition of NF-κB activation by proteasome inhibitors prevents the degradation of protein IκB, which accumulates in the cytosol, and there by the activation of NF-κB. Moreover, would not only limit the expression of adhesion molecules and cytokines involved in metastatic processes, but also increase the sensitivity of cancer cells to apoptosis. Considering this fact, the activity of NF-κB is regulated by the phosphorylation and proteasome-dependent degradation of its inhibitor Iκb. In this scenario, the use of a proteasome inhibitor might be an effective strategy in the treatment of skin cancer with constitutive activation of NF-κB.

摘要

泛素-蛋白酶体系统在与应激相关的信号转导中发挥核心作用,特别是在皮肤中通过控制 NF-κB 途径发挥作用。在正常情况下,抑制蛋白 IκB 被激酶磷酸化,然后被泛素化,并最终在蛋白酶体中降解。本综述讨论了蛋白酶体抑制剂抑制 NF-κB 激活的最新进展,可防止抑制蛋白 IκB 的降解,该蛋白在细胞质中积累,从而激活 NF-κB。此外,这不仅限制了参与转移过程的黏附分子和细胞因子的表达,而且还增加了癌细胞对细胞凋亡的敏感性。鉴于这一事实,NF-κB 的活性受到其抑制剂 IκB 的磷酸化和蛋白酶体依赖性降解的调节。在这种情况下,使用蛋白酶体抑制剂可能是治疗 NF-κB 持续激活的皮肤癌的有效策略。

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