Guo Yuening, Chi Xiaowen, Qu Si'ying, Sun Yu, Liu Jing, Zhang Lijuan, Cao Caihong, Wang Yansha, Zhang Wei
Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, Heilongjiang, China.
Department of Pediatric, The First Affiliated Hospital of Harbin Medical University, Harbin 150001, Heilongjiang, China.
Acta Histochem. 2022 Jan;124(1):151818. doi: 10.1016/j.acthis.2021.151818. Epub 2021 Dec 29.
This study aimed to explore the role of MIB2 in non-small cell lung cancer (NSCLC) and the underlying mechanism. Quantitative real-time PCR (QRT-PCR) and western blot were first performed to detect MIB2 expression in tumor tissues obtained from NSCLC patients (n = 30) and NSCLC cells, respectively. 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide (MTT) and transwell assays were then used to examine the effect of MIB2 on the proliferation, migration and invasion of NSCLC cells. Western blot was further performed to examine the effect of Mind bomb 2 (MIB2), an E3 ligase on Notch1 protein and its ubiquitination. MIB2 was significantly down-regulated in NSCLC tissues and cells, both in mRNA and protein level. MIB2 also note worthily inhibited the proliferation, migration, and invasion of NSCLC cells. Furthermore, MIB2 only down-regulated Notch1 protein level, while facilitated the ubiquitination of Notch1. Additionally, Notch1 significantly relieved the repressed proliferation, migration and invasion of NSCLC cells induced by MIB2. Conclusively, MIB2 inhibited cell proliferation, migration and invasion via inducing Notch1 ubiquitination and degradation in NSCLC.
本研究旨在探讨MIB2在非小细胞肺癌(NSCLC)中的作用及其潜在机制。首先进行定量实时PCR(QRT-PCR)和蛋白质印迹法,分别检测从NSCLC患者(n = 30)获得的肿瘤组织及NSCLC细胞中MIB2的表达。然后采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法和Transwell实验检测MIB2对NSCLC细胞增殖、迁移和侵袭的影响。进一步通过蛋白质印迹法检测E3连接酶Mind bomb 2(MIB2)对Notch1蛋白及其泛素化的影响。在NSCLC组织和细胞中,MIB2在mRNA和蛋白质水平均显著下调。MIB2还显著抑制了NSCLC细胞的增殖、迁移和侵袭。此外,MIB2仅下调Notch1蛋白水平,同时促进Notch1的泛素化。另外,Notch1显著缓解了MIB2诱导的NSCLC细胞增殖、迁移和侵袭的抑制作用。总之,MIB2通过诱导NSCLC中Notch1的泛素化和降解来抑制细胞增殖、迁移和侵袭。