UCH-L3对乳腺癌生物学行为的影响:与HIF-1α表达的相关性

Yang Zheng, Jinlong Zhong, G. Ren, Wei Sun, Jing Wu, Qirong Li, Yue Zhang, J. Zhao, Hai-hui Ling, Ying-xu Shi, Gaowa Share, Xiaoyan Xu, H. Du, Yonghong Shi
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引用次数: 1

摘要

推测:HIF-1α在三阴性乳腺癌细胞系(MDA-MB-231)中高表达,缺乏ER、PR和HER2的表达,具有较高的侵袭转移能力。先前的研究发现,靶向MDA-MB-231中HIF-1α的siRNA抑制了细胞的生长和迁移、侵袭能力,促进了细胞凋亡。UCH-L3蛋白是双向凝胶电泳和蛋白质组学检测到的HIF-1α siRNA细胞与非siRNA细胞的差异蛋白之一。本研究旨在探讨UCH-L3对三阴性乳腺癌细胞株(MDA-MB-231)生物学行为的影响。方法:分别用慢病毒组成载体和靶向UCH-L3的siRNA转染UCH-L3,建立UCH-L3的过表达和阻断表达。采用实时定量PCR和Western blot或Co-ip检测mRNA和蛋白。CCK8和克隆形成试验评估细胞生长和克隆性。采用Matrigel Transwell和will Scratch实验评估细胞侵袭和迁移率。结果:在慢病毒载体的MDA-MB-231细胞中,UCH-L3的过表达抑制了细胞的生长和克隆,削弱了细胞的迁移和侵袭能力,降低了游离和泛素化HIF-1α的表达。应用蛋白水解酶抑制剂MG132可提高UCH-L3过表达细胞中UCH-L3蛋白水平,但仍可降低UCH-L3过表达细胞中HIF-1α蛋白水平。siRNA技术阻断UCH-L3表达可使HIF-1α表达正常升高。结论:UCH-L3高表达对三阴性乳腺癌细胞的生物学行为有抑制作用,对HIF-1α表达有负作用,提示UCH-L3可能是三阴性乳腺癌的一种治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effects of UCH-L3 on the Biological Behaviours of Breast Cancer: Correlation with the Expressions of HIF-1α
Projective: HIF-1α is highly expressed in the triple negative breast cancer cell line (MDA-MB-231), which is lack of the expression of ER,PR and HER2 and exhibits high invasive and metastatic ability. Previous study detected that siRNA targeting HIF-1α in MDA-MB-231 restrained the cell growth and the abilities of immigration and invasion, and promoted apoptosis. UCH-L3 protein was found to be one of the differential proteins detected by Bidirectional gel Electrophoresis and Proteomics in the cells with HIF-1α siRNA cells comparing to no-siRNA cells. The objective of this study is to probe the effect of UCH-L3 on the biological behaviors of the triple negative breast cancer cell line (MDA-MB-231). Methods: Over or blocking expressions of UCH-L3 were established by the transfections with lentiviral constitutive vector and siRNA targeting UCH-L3 respectively. Real time quantitative PCR and Western blot or Co-ip were used to detect the mRNA and proteins. CCK8, and clone formation assays were to evaluate the cell growth and clonality. Matrigel Transwell and Would Scratch assay were used to estimate the cell invasion and mobility. Results: The over-expression of UCH-L3 inhibited the cell growth and clonality, weaken the abilities of cell immigration and invasion, and lowered the expression of free and ubiquitined HIF-1α in MDA-MB-231 cells with lentiviral vector comparing to those in the cells with control vector. Application of proteolytic enzyme inhibitor, MG132 increased the protein level of UCH-L3 but still decreased the protein level of HIF-1α in the cells with UCH-L3 over-expression. Blocking UCH-L3 expression by siRNA technique increased the expression of HIF-1α properly. Conclusion: high expression of UCH-L3 showed an inhibitory effect on the biological behaviors of triple negative breast cancer cell and negative effect on HIF-1α expression, implying that UCH-L3 likely to be a therapeutic strategy for triple negative breast cancer.
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