癌变·畸变·突变 ›› 2015, Vol. 27 ›› Issue (2): 134-136,141.doi: 10.3969/j.issn.1004-616x.2015.02.012

• 论著 • 上一篇    下一篇

nm23-H1基因转染对肺癌L9981细胞黏附分子表达的影响

郑海霞1, 崔永言2, 申东兰3, 彭安3, 何艳玲3   

  1. 1. 北京大学深圳医院体检科, 广东 深圳 518036;
    2. 北京大学深圳医院整形外科, 广东 深圳 518036;
    3. 北京大学深圳医院肿瘤内科, 广东 深圳 518036
  • 收稿日期:2014-06-04 修回日期:2014-12-03 出版日期:2015-03-31 发布日期:2015-03-31
  • 通讯作者: 崔永言,E-mail:cyy8188@163.com E-mail:cyy8188@163.com
  • 作者简介:郑海霞,Tel:13828736582,E-mail:zhenghx200878@163.com
  • 基金资助:

    国家自然科学基金资助项目(30070333)

Influences of nm23-H1 gene transfection on expressions of adhesion molecules in lung cancer cell line L9981

ZHENG Haixia1, CUI Yongyan2, SHEN Donglan3, PENG An3, HE Yanling3   

  1. 1. Department of Health Examination, Peking University Shenzhen Hospital, Shenzhen 518036;
    2. Department of Plastic Surgery, Peking University Shenzhen Hospital, Shenzhen 518036;
    3. Department of Oncology, Peking University Shenzhen Hospital, Shenzhen 518036, Guangdong, China
  • Received:2014-06-04 Revised:2014-12-03 Online:2015-03-31 Published:2015-03-31
  • About author:10.3969/j.issn.1004-616x.2015.02.012

摘要:

目的:探讨nm23-H1基因转染对肺癌L9981细胞黏附分子表达的影响。方法:利用细胞黏附实验、Boyden小室法研究转染前后肺癌L9981细胞黏附、侵袭能力的改变。分别利用逆转录-PCR(RT-PCR)和流式细胞术检测转染前后E-cadherin、integrin β1和integrin β3 mRNA和蛋白的表达。结果:转染后L9981细胞株黏附性以及侵袭性均降低。与转染空载体组相比,转染nm23-H1质粒后L9981细胞E-cadherin mRNA和蛋白表达均增强,integrin β1和integrin β3 mRNA和蛋白表达均减弱,差异均具有统计学意义(P均<0.05)。结论:nm23-H1基因具有逆转肺癌恶性转移表型的能力,其对肺癌L9981细胞株E-cadherin表达具有正调控作用,对integrin β1和integrin β3表达具有负调控作用。

关键词: nm23-H1, 肺癌细胞, 钙调素, 整合素, 肿瘤转移

Abstract:

OBJECTIVE:To study influences of nm23-H1 gene transfection on the expressions of adhesion molecules in lung cancer cell line L9981. METHODS:Cell adhesion experiment and Boyden room were used to evaluate the change of cell adhesion and invasion. Semi-RT-PCR and flow cytometry were used to detect the mRNA and protein expressions of E-cadherin, integrin β1 and integrin β3 betwteen transfected and non-transfected cell lines. RESULTS: nm23-H1 cell line in vitro adhesion and invasion were all down-regulated. mRNA of E-cadherin in the transfected cell line was stronger than that of non-transfected cell line, but mRNAs of integrin β1 and integrin β3 of transfected cell line were weaker than that of non-transfected cell line. Flow cytometry showed similar results as above. CONCLUSION: nm23-H1 could reverse lung cancer malignant phenotype. nm23-H1 could up-regulate E-cadherin expression, while down-regulate expressions of integrins β1 and β3, thus inhibit the metastasis of lung cancer cells.

Key words: nm23-H1, lung cancer cells, E-cadherin, integrins, neoplastic metastasis

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