实用医学杂志 ›› 2021, Vol. 37 ›› Issue (3): 291-297.doi: 10.3969/j.issn.1006⁃5725.2021.03.004

• 基础研究 • 上一篇    下一篇

NEK2在肝细胞癌中的表达及对增殖转移能力的影响

陶雪梅,阮浩宇,左乔竹,庞智,周春立
  

  1. 1 南京医科大学附属苏州医院消化内科(江苏苏州 215000);2 江苏省人民医院检验科(南京 210029);3 上海交通大学医学院附属仁济医院 上海市肿瘤研究所(上海 200120)
  • 出版日期:2021-02-10 发布日期:2021-02-10
  • 基金资助:
    国家自然科学基金面上项目(编号:81572311)

Expression of NEK2 in hepatocellular carcinoma and its effect on proliferation and metastasis

TAO Xue⁃mei,RUAN Haoyu,ZUO Qiaozhu,PANG Zhi,ZHOU Chunli
  

  1. Department of Gastroenterology,Suzhou munici⁃pal Hospital,Suzhou 215000,China
  • Online:2021-02-10 Published:2021-02-10

摘要:

目的 检测 NEK2 在肝癌中的表达并探讨其对肝癌细胞增殖转移能力的影响。方法 收集肝癌及其配对的癌旁组织,分别采用 qRT⁃PCR Western blot 检测NEK2mRNA 和蛋白水平的表达。利用公开的 GEPIA 数据库分析 NEK2 与肝癌预后的关系。通过慢病毒包装构建 NEK2 过表达和干扰的稳转 细胞株,采用 CCK⁃8 法检测 NEK2 对肝癌细胞增殖功能的影响,transwell 小室法检测 NEK2 对肝癌细胞迁移 和侵袭能力的影响。GEPIA 数据库分析 NEK2 与上皮细胞⁃间充质转化(epithelial⁃mesenchymal transition EMT)相关分子的关系。结果 在mRNA和蛋白水平,NEK2的表达均高于其癌旁组织(P < 0.05)。GEPIA 据库显示在 NEK2 相对高表达的肝癌患者中总体生存率(overall survival,OS)及无病生存率(disease⁃free survival,DFS)较差(P < 0.05)。体外实验证实过表达 NEK2 能够促进肝癌细胞的增殖及迁移侵袭功能;相 反,干扰 NEK2 的表达能够抑制肝癌细胞的增殖及迁移侵袭功能。GEPIA 数据库显示 NEK2 Twist1 Vim、FN1、TJP1、TGFB1、CDH1、CD44、JUP 正相关。结论 NEK2 在肝癌中表达增加,促进肝癌细胞恶性生 物学行为,且与EMT 表型有关,在评估肝癌患者预后方面具有一定的意义。

关键词:

Abstract: Objective We aim to detect the expression of NEK2 in hepatocellular carcinoma(HCC). The effects of NEK2 on proliferation,invasion and migration of HCC were also evaluated. Methods qRT ⁃ PCR and western blot were performed to detect the expression of NEK2 in paired HCC tissues compared to corresponding non⁃ tumorous liver tissues. We used publicly available data from GEPIA to evaluate the correlation of NEK2 with prog⁃ nosis in HCC. Stable NEK2 overexpression cell lines and knockdown cell lines were established. Cell proliferation was investigated by CCK⁃8 assays. Migratory and invasive abilities were conducted by transwell arrays. GEPIA was used to compare NEK2 expression with EMT markers. Results mRNA and protein level of NEK2 were both signififi cantly increased in HCC tissues compared to corresponding non⁃tumorous liver tissues(P < 0.05). GEPIA data indicates that patients in high NEK2 group show poorer OS and DFS(< 0.05). Stable overexpression of NEK2 promoted proliferation,migration and invasion of HCC cells,whereas silencing of NEK2 inhibited proliferation migration and invasion of HCC cells in vitro. GEPIA data indicates that the expression of NEK2 was positively correlated with EMT markers(Twist1,Vim,FN1,TJP1,TGFB1,CDH1,CD44 and JUP). Conclusions These fifindings indicate that NEK2 promotes malignant biological behavior of HCC. The expression of NEK2 was positively correlated with EMT markers and may serve as a target for HCC diagnosis and prognosis.

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