实用肿瘤学杂志 ›› 2018, Vol. 32 ›› Issue (6): 515-519.doi: 10.11904/j.issn.1002-3070.2018.06.007

• 基础研究 • 上一篇    下一篇

TRAP1在食管癌发展中的作用及机制研究

于芳, 赵培   

  1. 河北省人民医院检验科(石家庄 050051)
  • 收稿日期:2018-08-13 出版日期:2018-12-28 发布日期:2018-12-27
  • 通讯作者: 于芳, E-mail:yf_1218@126.com
  • 作者简介:于芳, 女, (1981-), 硕士, 主管检验师, 从事临床检验的研究。

The role and mechanism of TRAP1 in the development of esophageal cancer

YU Fang, ZHAO Pei   

  1. Department of Clinical Laboratory, Hebei General Hospital, Shijiazhuang 050051, China
  • Received:2018-08-13 Online:2018-12-28 Published:2018-12-27

摘要: 目的 探究肿瘤坏死因子受体相关蛋白1(TRAP1)在人食管癌进展中的作用及机制。方法 用免疫组化检测人食管癌组织中TRAP1和S100A8的表达水平。在食管癌细胞系KYSE150中建立稳定下调TRAP1的细胞系, 用CCK-8检测细胞的增殖能力, Transwell检测细胞的转移能力, 流式细胞术检测细胞的凋亡。用实时荧光定量PCR检测TRAP1的下游基因E-Cadherin、N-Cadherin和S100A8的表达水平。结果 TRAP1在食管癌组织中的表达水平(55.0%)显著高于癌旁组织(11.7%), 并与S100A8具有一致性(χ2=4.141, P<0.001)。得到稳定下调TRAP1的细胞系KYSE150-TRAP1, 与对照组细胞系KYSE150-control相比, KYSE150-TRAP1细胞系中TRAP1的表达水平下调85%(P<0.05), 细胞的转移能力降低46%(P<0.05), 细胞的增殖和凋亡无显著变化;E-Cadherin的表达水平升高19%(P<0.05), S100A8的表达水平下降39%(P<0.05)。结论 TRAP1在食管癌组织中过表达, 并通过调控S100A8的表达促进食管癌的转移。

关键词: 食管癌, 肿瘤坏死因子受体相关蛋白1, S100A8, 转移

Abstract: Objective The aim of this study was to investigate the role and mechanism of tumor necrosis factor receptor-related protein 1(TRAP1)in the progression of human esophageal cancer. Methods Immunohistochemistry was used to detect the expression of TRAP1 and S100A8 in human esophageal cancer tissues.A stably knocked-down TRAP1 cell line was established in the esophageal cancer KYSE150 cell line, the proliferation ability was detected by CCK-8, the transfer ability was detected by Transwell, and apoptosis was detected by flow cytometry.We conducted a gene profiling study to detect the expression of genes related to tumor progression.The expression of TRAP1 downstream genes-E-Cadherin, N-Cadherin and S100A8 was detected by Real-Time fluorescent quantitative PCR. Results The expression of TRAP1 in esophageal carcinoma was significantly higher than that in adjacent tissues and correlated with S100A8(χ2=4.141, P<0.001).The KYSE150 cell line with down-regulated of TRAP1(KYSE150-TRAP1)was established, and the expression of TRAP1 was down-regulated by 85%, cell invaded ability was decreased by 46%, no changes of cell proliferation and apoptosis were observed, when compared to the KYSE150 control cells.The expression level of E-cadherin was increased by 19%, and the expression level of S100A8 was decreased by 39% in KYSE150-TRAP1 cells. Conclusion TRAP1 is overexpressed in esophageal carcinoma and promotes the metastasis of esophageal carcinoma by regulating S100A8 expression.

Key words: Esophageal cancer, TRAP1, S100A8, Metastasis

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