癌变·畸变·突变 ›› 2016, Vol. 28 ›› Issue (4): 273-276,280.doi: 10.3969/j.issn.1004-616x.2016.04.005

• 论著 • 上一篇    下一篇

冈田酸对喉鳞癌细胞系PP2A活性及迁移的影响

童宇圣1, 陈涛1, 王聪慧1, 袁晖2, 徐立红3, 林志宏2   

  1. 1. 浙江大学医学院临床医学二系, 浙江 杭州 310058;
    2. 浙江大学医学院附属第二医院耳鼻喉科, 浙江 杭州 310058;
    3. 浙江大学医学院生物化学系, 浙江 杭州 310058
  • 收稿日期:2015-10-27 修回日期:2016-03-21 出版日期:2016-07-31 发布日期:2016-07-31
  • 通讯作者: 林志宏,E-mail:lzh@163.com E-mail:lzh@163.com
  • 作者简介:童宇圣,E-mail:tongys@zju.edu.cn;Tel:0571-88208265
  • 基金资助:
    浙江省自然科学基金(LY13H130001);浙江省科技厅项目(2013C33208);浙江省中医药管理局项目(2012ZA085)

Okadaic acid inhibits PP2A activities and cell migration of laryngeal squamous cell carcinoma Hep-2

TONG Yusheng1, CHEN Tao1, WANG Conghui1, YUAN Hui2, XU Lihong3, LIN Zhihong2   

  1. 1. The Second Department of Clinical Medicine, Zhejiang University School of Medicine, Hangzhou 310058;
    2. The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310058;
    3. Department of Biochemistry, Zhejiang University School of Medicine, Hangzhou 310058, Zhejiang, China
  • Received:2015-10-27 Revised:2016-03-21 Online:2016-07-31 Published:2016-07-31

摘要: 目的:探讨冈田酸(OA)对喉鳞癌细胞系(Hep-2)活性和迁移能力的影响及其可能的作用机制。方法:采用四甲基噻唑蓝(MTT)比色实验确定OA作用于Hep-2的最大浓度;酶活性实验检测不同浓度(0、50、100 nmol/L) OA对Hep-2蛋白磷酸酶2A (PP2A)活性的影响;划痕实验检测Hep-2在不同浓度(0、50、100 nmol/L) OA作用下迁移能力的变化。结果:50、100、200 nmol/L OA作用24 h后Hep-2的相对活力分别为96.7%±1.8%、82.9%±12.6%和57.2%±7.7%,与对照组(100%)比较均明显下降(P均<0.05)。50和100 nmol/L OA作用24 h后PP2A的相对活性分别为30.90%±12.01%和8.98%±4.96%,与对照组(100%)相比明显下降(P<0.05)。划痕试验中,经OA作用24及48 h后Hep-2细胞的迁移能力与对照组相比均明显减弱(P<0.05),并且100 nmol/L OA处理组迁移能力的减弱程度较50 nmol/L OA处理组更明显(P<0.05)。结论:100 nmol/L冈田酸明显抑制Hep-2细胞PP2A活性并降低了细胞的迁移能力。

关键词: 冈田酸, Hep-2细胞系, 喉鳞状细胞癌, 蛋白磷酸酶2A, 迁移

Abstract: OBJECTIVE: To investigate the mechanism of inhibition of Hep-2 cell migration by Okadaic acid (OA). METHODS: MTT assay was used to determine the doses of OA for the investigation. Hep-2 cells were treated with 0, 50 or 100 nmol/L OA and enzyme assay was used to measure PP2A activities. Wound scratch assay was used to observe the influence of OA on migration of Hep-2. RESULTS: The growth inhibition ratio was 96.7%±1.8%, 82.9%±12.6% and 57.2%±7.7% in cells treated with 50, 100 and 200 nmol/L OA, and the difference was significant (P<0.05). In cells treated with 50 and 100 nmol/L OA, the relative activity of PP2A was 30.90%±12.01% and 8.98%±4.96% (P<0.05). From the wound scratch assay, the treated cells took significantly longer than untreated cells for healing (P<0.05). CONCLUSION: Inhibition of PP2A activities may be responsible for the reduction of migration in the OA-treated Hep-2 cells.

Key words: Okadaic acid, Hep-2, laryngeal squamous cell carcinoma, protein phosphatase 2A, migration

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