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转化生长因子β诱导的基因抑制恶性间皮瘤细胞增殖的体外研究

曹艳梅, 张鹤美, 高四海, 贺金奖, 童 建, 张增利, Tom K Hei, 李冰燕

曹艳梅, 张鹤美, 高四海, 贺金奖, 童 建, 张增利, Tom K Hei, 李冰燕. 转化生长因子β诱导的基因抑制恶性间皮瘤细胞增殖的体外研究[J]. 肿瘤防治研究, 2013, 40(12): 1123-1127. DOI: 10.3971/j.issn.1000-8578.2013.12.004
引用本文: 曹艳梅, 张鹤美, 高四海, 贺金奖, 童 建, 张增利, Tom K Hei, 李冰燕. 转化生长因子β诱导的基因抑制恶性间皮瘤细胞增殖的体外研究[J]. 肿瘤防治研究, 2013, 40(12): 1123-1127. DOI: 10.3971/j.issn.1000-8578.2013.12.004
CAO Yanmei, ZHANG Hemei, GAO Sihai, HE Jinjiang, TONG Jian, ZHANG Zengli, Tom K Hei, LI Bingyan. Transforming Growth Factor-β Induced Gene Inhibits Cell Proliferation of Malignant Mesothelioma in vitro[J]. Cancer Research on Prevention and Treatment, 2013, 40(12): 1123-1127. DOI: 10.3971/j.issn.1000-8578.2013.12.004
Citation: CAO Yanmei, ZHANG Hemei, GAO Sihai, HE Jinjiang, TONG Jian, ZHANG Zengli, Tom K Hei, LI Bingyan. Transforming Growth Factor-β Induced Gene Inhibits Cell Proliferation of Malignant Mesothelioma in vitro[J]. Cancer Research on Prevention and Treatment, 2013, 40(12): 1123-1127. DOI: 10.3971/j.issn.1000-8578.2013.12.004

转化生长因子β诱导的基因抑制恶性间皮瘤细胞增殖的体外研究

基金项目: 国家自然科学基金资助项目(81072286);江苏省自然科学基金资助项目(SBK201221995)
详细信息
    作者简介:

    曹艳梅(1985-),女,硕士在读,主要从事卵巢癌的防治研究

    通讯作者:

    李冰燕,E-mail:bingyanli@suda.edu.cn

  • 中图分类号: R73-3

Transforming Growth Factor-β Induced Gene Inhibits Cell Proliferation of Malignant Mesothelioma in vitro

  • 摘要: 目的 研究转化生长因子β诱导的基因 (transforming growth factor-β induced gene, TGFBI) 在体外是否能抑制恶性间皮瘤细胞NCI-H28的增殖。方法 将外源性TGFBI稳定性转染到恶性间皮瘤细胞NCI-H28中,绘制生长曲线图,测定其细胞增殖、接种效率和软琼脂克隆形成,并进行细胞周期的分析。结果 外源性TGFBI在恶性间皮瘤细胞NCI-H28中能够稳定地高表达;当外源性的TGFBI 转入到肿瘤细胞NCI-H28后,TGFBI高表达的细胞倍增时间增加了4.38倍;与转染空载体的肿瘤细胞相比:NCI-H28的相对接种效率降低了69.68 %,外源性TGFBI表达的T28细胞形成了较小的软琼脂克隆;TGFBI可以使肿瘤细胞阻滞在G1期,并延缓肿瘤细胞进入S期的时间。结论 TGFBI可以抑制恶性间皮瘤细胞的体外增殖。

     

    Abstract: Objective To explore that transforming growth factor-β induced gene (TGFBI) inhibits NCI-H28 growth in vitro. Methods TGFBI was stably transfected into mesothelioma cell line NCI-H28. growth curve, cell proliferation, platting effi ciency, and colony formation in soft agar were analyzed. Results Exogenous TGFBI in malignant mesothelioma NCI-H28 had a high expression in stably. After exogenous TGFBI transferred into tumor cells NCI-H28, doubling time of TGFBI high expression cell was increased by 4.38 times, compared with the empty vector. Relative plating effi ciency of NCI-H28 was decreased by 69.68%. T28 cells with exogenous TGFBI formed a smaller soft agar; TGFBI made tumor cells arrest in G1 phase and delay tumor cells into the S phase . Conclusion TGFBI was able to inhibit the cell proliferation of malignant mesothelioma in vitro.

     

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出版历程
  • 收稿日期:  2012-09-18
  • 修回日期:  2013-01-17
  • 刊出日期:  2013-12-24

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