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CCAAT/增强子结合蛋白β介导的MMP3上调促进食管鳞状细胞癌侵袭并与人患者的转移相关。

CCAAT/Enhancer Binding Protein β-Mediated MMP3 Upregulation Promotes Esophageal Squamous Cell Cancer Invasion and Is Associated with Metastasis in Human Patients.

作者信息

Li Hong, Yang Fan, Chai Li, Zhang Liguo, Li Sha, Xu Ziguang, Kong Lingfei

机构信息

1 Department of Oncology, Henan Cancer Hospital, Zhengzhou University, Zhengzhou, Henan Province, People's Republic of China.

2 Department of Computer Science, University of Nebraska-Lincoln, Lincoln, Nebraska.

出版信息

Genet Test Mol Biomarkers. 2019 May;23(5):304-309. doi: 10.1089/gtmb.2018.0291. Epub 2019 Apr 10.

DOI:10.1089/gtmb.2018.0291
PMID:30969151
Abstract

Metastasis is a significant obstacle to curing esophageal squamous cell carcinoma (ESCC). The CCAAT/enhancer binding protein β (C/EBPβ) and matrix metalloproteinase 3 (MMP3) are thought to play key roles in cancer invasion and metastasis. In this study, we aimed to detect whether C/EBPβ-mediated tumor invasion was dependent on MMP3. In addition, we determined whether C/EBPβ upregulation was associated with MMP3 levels and metastatic status in patients with ESCC. A total of 126 patients with ESCC were recruited for this study. The mRNA and protein levels of C/EBPβ and MMP3 in ESCC cell lines and specimens from ESCC patient were determined by reverse transcription-polymerase chain reaction and western blot, respectively. Tumor cell invasion was analyzed using an Matrigel Invasion Assay. The correlation between C/EBPβ and MMP3 expression was determined by Pearson's correlation analysis. Both mRNA and protein levels of MMP3 were upregulated by C/EBPβ overexpression and downregulated by C/EBPβ siRNA in KYSE150 cell cultures. The promotion of ESCC cell invasion through C/EBPβ was inhibited by MMP3 siRNA. The level of C/EBPβ was correlated with MMP3 and metastatic status in patients with ESCC. C/EBPβ upregulation promoted tumor cell invasion in an MMP3-dependent manner and was associated with metastatic status in ESCC.

摘要

转移是食管癌鳞状细胞癌(ESCC)治愈的重大障碍。CCAAT/增强子结合蛋白β(C/EBPβ)和基质金属蛋白酶3(MMP3)被认为在癌症侵袭和转移中起关键作用。在本研究中,我们旨在检测C/EBPβ介导的肿瘤侵袭是否依赖于MMP3。此外,我们还确定了C/EBPβ上调是否与ESCC患者的MMP3水平和转移状态相关。本研究共招募了126例ESCC患者。分别通过逆转录-聚合酶链反应和蛋白质印迹法测定ESCC细胞系和ESCC患者标本中C/EBPβ和MMP3的mRNA和蛋白质水平。使用基质胶侵袭试验分析肿瘤细胞侵袭。通过Pearson相关分析确定C/EBPβ与MMP3表达之间的相关性。在KYSE150细胞培养物中,C/EBPβ过表达上调MMP3的mRNA和蛋白质水平,而C/EBPβ siRNA下调其水平。MMP3 siRNA抑制了通过C/EBPβ促进的ESCC细胞侵袭。ESCC患者中C/EBPβ水平与MMP3和转移状态相关。C/EBPβ上调以MMP3依赖的方式促进肿瘤细胞侵袭,并与ESCC的转移状态相关。

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