癌变·畸变·突变 ›› 2021, Vol. 33 ›› Issue (3): 203-207,224.doi: 10.3969/j.issn.1004-616x.2021.03.008

• 论著 • 上一篇    下一篇

NEDD4在食管鳞癌中的表达及作用研究

郑珺文, 常晨, 郝佳洁, 蔡岩, 王明荣, 张钰   

  1. 国家癌症中心/国家肿瘤临床医学研究中心/中国医学科学院北京协和医学院肿瘤医院, 分子肿瘤学国家重点实验室, 北京 100021
  • 收稿日期:2021-03-31 修回日期:2021-04-20 出版日期:2021-05-30 发布日期:2021-06-09
  • 通讯作者: 张钰,E-mail:zhangyu909@126.com。 E-mail:zhangyu909@126.com
  • 作者简介:郑珺文,E-mail:junwenzheng_tate@126.com。
  • 基金资助:
    国家自然科学基金(81872279);中央高校基本科研业务费国家重点实验室优秀骨干项目(2012S09)

Investigation on expression and function of NEDD4 in esophageal squamous cell carcinoma

ZHENG Junwen, CHANG Chen, HAO Jiajie, CAI Yan, WANG Mingrong, ZHANG Yu   

  1. State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China
  • Received:2021-03-31 Revised:2021-04-20 Online:2021-05-30 Published:2021-06-09

摘要: 目的:检测神经前体细胞表达发育下调蛋白4(neural precursor cell expressed developmentally down-regulated protein 4,NEDD4)在食管鳞癌组织中的表达及其临床意义,并探讨其过表达对食管鳞癌细胞恶性表型的影响。方法:应用组织芯片-免疫组织化学染色技术,检测131例食管鳞癌及配对癌旁正常食管上皮组织中NEDD4蛋白的表达情况,并分析其表达水平与临床病理指标的相关性;同时,使用TCGA和GTEx数据库中的mRNA表达数据,分析食管鳞癌组织中NEDD4 mRNA的表达变化。然后,在NEDD4表达水平较高的食管鳞癌细胞系中用特异性siRNA敲降NEDD4的表达,采用CCK8法检测细胞增殖活力的变化。结果:免疫组化染色结果显示,NEDD4在40%(53/131)的食管鳞癌组织中高水平表达,而在癌旁正常食管上皮组织中不表达或低水平表达。NEDD4蛋白的表达水平与食管鳞癌的浸润深度、病理学分期呈正相关(均为P < 0.05)。同时,TCGA及GTEx数据库分析结果显示,NEDD4 mRNA表达水平在食管鳞癌组织中明显升高(P < 0.01)。细胞增殖活力检测结果显示,在KYSE30和KYSE150细胞中,转染NEDD4 siRNA的实验组细胞的增殖活力均显著低于对照组细胞(均为P < 0.01)。结论:NEDD4在食管鳞癌组织中表达上调,其高表达可增强食管鳞癌细胞的增殖活力,提示NEDD4过表达可能在食管鳞癌的发生发展过程中发挥促癌作用。

关键词: 食管鳞癌, 神经前体细胞表达发育下调蛋白4, 细胞增殖, 促癌作用

Abstract: OBJECTIVE: To investigate expression status, clinical implication, and functional role of neural precursor cell expressed developmentally down-regulated protein 4 (NEDD4) in esophageal squamous cell carcinoma (ESCC). METHODS: Protein expression of NEDD4 was examined by immunohistochemistry (IHC) in tissue microarrays containing 131 ESCC specimens. Correlations between NEDD4 expression levels and the clinicopathological parameters were analyzed using Pearson Chi- Square and Fisher exact tests. Alterations of NEDD4 mRNA level in ESCC specimens were evaluated using data from the TCGA and GTEx databases. Furthermore, NEDD4 expression was knocked down in ESCC cell lines which had high NEDD4 expressions and changes of cell proliferation activity were detected using the CCK8 assay. RESULTS: Over-expressions of NEDD4 were detected in 40% (53/131) of ESCC specimens,while it was not expressed or expressed at a low level in adjacent normal epithelial tissues. In addition,NEDD4 protein levels were significantly correlated with pathologic T stage and histological grades of ESCC (P < 0.05,respectively). TCGA and GTEX database analysis results show that NEDD4 mRNA levels were also prominently up-regulated in ESCC specimens (P < 0.01). Data of the CCK8 assay further demonstrate that knockdown of NEDD4 expression significantly suppressed the proliferation capacities of KYSE150 and KTSE30 cells in vitro (P < 0.01). CONCLUSION: NEDD4 was frequently up- regulated in ESCC, and its over- expression enhanced proliferation ability of ESCC cells. Our data suggest that abnormal expression of NEDD4 played an oncogenic role in the occurrence and development of ESCC.

Key words: esophageal squamous cell carcinoma, NEDD4, cell proliferation, cancer-promoting effect

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