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苦参碱体外诱导卵巢癌3AO细胞凋亡的研究 被引量:5

Matrine induced apoptosis in ovarian cancer cell line 3AO
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摘要 目的:观察中药苦参碱对卵巢癌3AO细胞的增殖抑制作用。方法:应用不同浓度的苦参碱作用3AO细胞,分别用倒置显微镜观察细胞形态学改变;MTT法检测苦参碱对3AO细胞的增殖抑制作用;流式细胞仪检测苦参碱对3AO细胞凋亡的影响。结果:苦参碱具有抑制卵巢癌3AO细胞增殖的作用,并呈明显的时间-剂量依赖性;在苦参碱作用下,3AO细胞出现凋亡改变;FCM检测结果显示经苦参碱作用后,细胞的凋亡率增加,呈现时间-剂量依赖性。结论:苦参碱能诱导卵巢癌细胞凋亡,抑制卵巢癌细胞增殖。 Objective:To study the effect of matrine on the apoptosis of ovarian cancer cell at different concentrations.Methods:Matrine at different concentrations was respectively used to cultivate 3AO in vitro.Cell proliferation was assessed by MTT assays.Morphological changes of apoptosis were observed with invert microscope.Cell cycle were examined by PI fluorescence flow cytometry ( FCM) respectively.Results:Inhibition of matrine on the growth of 3AO cell was increasing with passing of time and increasing of concentration.Under the influence of matrine,3AO cell exhibited changes of apoptosis in morphology of microscope.Conclusion:matrine can inhibit cell proliferation and induces apoptosis in ovarian cancer cell line.
出处 《中药药理与临床》 CAS CSCD 北大核心 2010年第3期20-22,共3页 Pharmacology and Clinics of Chinese Materia Medica
基金 四川卫生厅课题(03007)
关键词 苦参碱 增殖 凋亡 卵巢癌 matrine apoptosis ovarian cancer
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  • 1赵军艳,郑艳敏,赵红艳,姚树坤.苦参碱和氧化苦参碱对肝癌细胞增殖凋亡及JAK-STAT信号通路的影响[J].中药药理与临床,2008,24(4):18-20. 被引量:37
  • 2Liu XY, Fang H, Yang ZG, et al. Matrine inhibits invasiveness and metastasis of human malignant melanoma cell line A375 in vitro . Int J Dermatol, 2008;47(5): 448-456.
  • 3Ma L, Wen S, Zhan Y, et al. Anticancer effects of the Chinese medicine matrine on murine hepatoeellular carcinoma eeUs. Planta Med, 2008 ; 74 (3) : 245-251.
  • 4Luo C, Zhu Y, Jiang T, et al. Matrine induced gastric cancer MKN45 cells apoptosis via increasing pro-apoptotie molecules of Bel-2 family.. Toxicology, 2007 ;229( 3 ) : 245 - 252.
  • 5Dai Z J, Gao J, Ji ZZ. et al. Matrine induces apoptosis in gastric carcinoma cells via alteration of Fas/FasL and activation of caspase-3. Ethnopharmacol, 2009;123(1): 91 -96.
  • 6Hua J, Chun HH, Shu BZ, et al. Matrine upregulates the cell cycle protein E2F-1 and triggers apoptosis via the mitochondrial pathway in K562 cells Eur J Pharmacol, 2007 ;559:98 - 108.

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