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中国临床药理学与治疗学 ›› 2013, Vol. 18 ›› Issue (3): 271-275.

• 基础研究 • 上一篇    下一篇

柚皮苷对人卵巢癌SKOV3细胞环氧化酶2 mRNA及蛋白表达水平的影响

宋淑慧1, 胡昕1, 熊玉卿2, 蔡丽萍1   

  1. 1南昌大学第一附属医院妇产科
    2南昌大学医学院临床药理研究所,南昌 330006,江西
  • 收稿日期:2012-12-24 修回日期:2013-02-21 出版日期:2013-03-26 发布日期:2013-04-02
  • 通讯作者: 蔡丽萍,通信作者,女,教授,硕士生导师,研究方向为妇科肿瘤。Tel: 0791-88692550 E-mail: cailiping2550@163.com
  • 作者简介:宋淑慧,女,硕士研究生,研究方向为妇科肿瘤。Tel: 13576099845 E-mail: huishusong@126.com
  • 基金资助:
    国家十二五科技重大专项“构建国际标准的规范化药物临床试验研究与评价技术平台”(2011ZX09302-007-03)

Effects of Naringin on expression of COX-2 mRNA and protein in Human ovarian cancer cell line SKOV3

SONG Shu-hui1, HU Xin1, XIONG Yu-qing2, CAI Li-ping1   

  1. 1Department of Gynecology and Obstetrics, the First Affiliated Hospital of Nanchang University
    2Institute of Clinical Pharmacology, Medical College of Nanchang University, Nanchang 330006, Jiangxi, China
  • Received:2012-12-24 Revised:2013-02-21 Online:2013-03-26 Published:2013-04-02

摘要: 目的: 研究中药柚皮苷对人卵巢癌SKOV3细胞环氧化酶2(COX-2)mRNA及蛋白表达水平的影响。方法: 常规培养人卵巢癌SKOV3细胞,分为空白对照组、柚皮苷 10 μmol/L 组、柚皮苷 20 μmol/L 组、柚皮苷 40 μmol/L 组、阳性对照组(塞来昔布 80 μmol/L)。MTT法测定柚皮苷对人卵巢癌SKOV3细胞增殖的影响,运用Real-time PCR和Western Blot法测定培养48 h后各组细胞中COX-2 mRNA和蛋白表达水平的变化。结果: MTT检测法显示,柚皮苷各浓度处理组,时间依赖性和剂量依赖性地抑制人卵巢癌SKOV3细胞生长。经药物处理48 h后,Real-time PCR结果显示,与空白对照组(1.094±0.053)比较,10、20 μmol/L 柚皮苷即对SKOV3细胞COX-2 mRNA表达抑制作用(0.828±0.006,0.753±0.011,P<0.05),而 40 μmol/L 柚皮苷则明显下调 COX-2 mRNA的表达(0.412±0.216,P<0.01),与塞来昔布组(0.321±0.017)的抑制程度相近。Western Blot法检测结果显示,与空白对照组(1.7325±0.0826)相比,10 μmol/L 柚皮苷组相对表达量(1.7925±0.0880)虽略有上调,但无统计学差异,20、40 μmol/L 柚皮苷组均可明显下调SKOV3细胞COX-2蛋白的表达(1.2225±0.0822,1.2725±0.0763,P<0.05),塞来昔布组也明显抑制COX-2蛋白的表达。结论: 柚皮苷可抑制人卵巢癌SKOV3细胞体外增殖并抑制COX-2 mRNA和蛋白的表达。

关键词: 柚皮苷, 环氧化酶2, 人卵巢癌SKOV3细胞

Abstract: AIM: To investigate effects of naringin on expression of COX-2 mRNA and protein of Human ovarian cancer cell line SKOV3.METHODS: SKOV3 cells were cultured in vitro and divided into five groups randomly, namely control group, naringin group (10 μmol/L), naringin group (20 μmol/L), naringin group (40 μmol/L) and celecoxib group (80 μmol/L). The inhibition effects of naringin on cell- proliferation were determined by MTT method. The expression of COX-2 mRNA and protein were evaluated by Western Blot and Real-time quantitative PCR after forty-eight hours.RESULTS: Naringin could inhibit the growth of SKOV3 cells, and with the increase of the dosage and time, the tumor growth inhibition rate increased significantly (P<0.01).Compared with control group,the expression of COX-2 mRNA was down-regulated significantly by every dosage of naringin and celecoxib (0.828±0.006, 0.753±0.011, 0.412±0.216, 0.321±0.017). Meanwhile, the expression of COX-2 protein was down-regulated significantly by every dosage of naringin and celecoxib (1.7925±0.088, 1.2225±0.0822, 1.2725±0.07632, 0.3075±0.0977).CONCLUSION: The appropriate dosage of naringin can inhibit SKOV3 cells growth in vitro, and can down-regulate the expression of COX-2 mRNA and protein.

Key words: Naringin, COX-2, Human Ovarian cancer cell line SKOV3

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