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中国临床药理学与治疗学 ›› 2012, Vol. 17 ›› Issue (12): 1321-1326.

• 基础研究 •    下一篇

金雀异黄素通过调控miR-27a及其靶基因对卵巢癌细胞SKOV3生长的影响

徐琳琳1, 孙庆敏2, 罗璇1, 翟溯澜1, 李萍1, 赵小梅1, 王雪融1   

  1. 1南京医科大学基础医学院药理学系,南京 210029,江苏;
    2南京医科大学附属无锡市妇幼保健院药剂科,无锡 214002,江苏
  • 收稿日期:2012-09-16 修回日期:2012-11-09 发布日期:2012-12-31
  • 通讯作者: 王雪融,通信作者,女,博士,教授,研究方向:肿瘤药理。Tel: 13813385723 E-mail: wangxrnj@gmail.com
  • 作者简介:徐琳琳,女,硕士研究生,研究方向:肿瘤药理。Tel: 15996931516 E-mail: xulinlin16@163.com
  • 基金资助:
    国家自然科学基金项目(81001444; 30873099; 81102458; 81172004)

Effects of genistein on the growth of ovarian cancer cell SKOV3 by regulating miR-27a and target gene expression

XU Lin-lin1, SUN Qing-min2, LUO Xuan1, ZHAI Su-lan1, LI Ping1, ZHAO Xiao-mei1, WANG Xue-rong1   

  1. 1Department of Pharmacology, Nanjing Medical University, Nanjing 210029, Jiangsu, China;
    2Department of Pharmacy, Affiliated Wuxi Hospital for Maternal and Child Health Care of Nanjing Medical University, Wuxi 214002, Jiangsu, China
  • Received:2012-09-16 Revised:2012-11-09 Published:2012-12-31

摘要: 目的: 研究金雀异黄素对卵巢癌细胞株SKOV3生长的抑制作用及其可能的机制。方法: 收集卵巢癌组织及良性组织,应用RT-PCR法检测miR-27a的表达。用不同浓度的金雀异黄素处理细胞,通过SRB法检测金雀异黄素单用或加入miR-27a mimics后对细胞株生长的抑制作用;经RT-PCR和Western blot检测miR-27a及靶基因Sprouty2表达的变化。结果: miR-27a在卵巢癌组织中的表达高于良性组织(P<0.05)。金雀异黄素可呈浓度和时间依赖的方式抑制卵巢癌细胞SKOV3生长;金雀异黄素浓度依赖性地下调miR-27a,上调Sprouty2的表达,且miR-27a mimics能够部分拮抗金雀异黄素抑制细胞生长的作用。结论: 金雀异黄素可能通过下调致癌miR-27a的表达,发挥抑制卵巢癌细胞生长的作用。

关键词: 金雀异黄素, 卵巢癌, 生长, miR-27a, Sprouty2

Abstract: AIM: To investigate the effects of genistein on the growth of ovarian cancer cell SKOV3 and potential mechanism. METHODS: The expression of the miR-27a in formalin-fixed paraffin-embedded (FFPE) ovarian cancer tissues and benign ovarian tissues were examined by RT-PCR. SKOV3 cells were treated with different concentration of genistein. Then the SRB assays were performed to assess the growth inhibition of genistein to ovarian cancer cells. RT-PCR and Western blot were used to test expression of miR-27a and Sprouty2 respectively. RESULTS: The expression levels of miR-27a in FFPE ovarian cancer tissues were significantly higher than those seen in benign ovarian tissues. Genistein could markedly decrease human ovarian cancer cell growth in time- and dose- dependent manner and downregulate the expression of miR-27a, which was accompanied by significantly increased expression of Sprouty2. CONCLUSION: Genistein has an inhibitory effect on the growth of ovarian cancer cells, which was due to the downregulation of miR-27a expression.

Key words: Genistein, Ovarian cancer, Growth, MiR-27a, Sprouty2

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