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针对病种:卵巢癌

发表时间:2013年9月

发表国家:荷兰

登载刊物:药物化学中的抗癌药物

研究单位:中国江苏南京医科大学药理学院

研究人员:徐琳琳,向晶莹,沈建,等

主要结论:我们的研究结果揭示了致癌因子 miR-27a 在卵巢癌细胞生长和转移方面的重要作用,并且金雀异黄素,作为miRNA无毒的灭活剂,可以阻止卵巢癌细胞的生长和迁移,为金雀异黄素治疗活性的机制提供新的见解.

Anti-cancer agents in medicinal chemistry, 2013, 13(7):1126-32.

Oncogenic MicroRNA-27a is a Target for Genistein in Ovarian Cancer Cells

Linlin Xu, Jingying Xiang, Jian Shen, et al

Department of Pharmacology, Nanjing Medical University, Jiangsu, China

MicroRNAs (miRNAs) are emerging as important regulators in various pathobiological processes in cancer. Genistein, as a major isoflavonoid isolated from dietary soybean, possesses a wide variety of biological activities particularly in cancer prevention. However, the molecular mechanisms by which genistein elicits its effects on ovarian cancer cells have not been fully elucidated. In this study, we reported that expression of miR-27a was higher in human ovarian cancer relative to benign ovarian tissues. Meanwhile, transfection of SKOV3 cells with the inhibitor of miR-27a suppressed growth and migration of tumor cells. Our study also found that treatment of ovarian cancer cells with genistein caused an inhibition of ovarian cancer cell growth and migration. Further cellular mechanistic studies revealed that genistein down-regulated miR-27a expression, which was accompanied by significantly increased expression of Sprouty2, a putative miR-27a target gene. Taken together, our findings reveal that oncogenic miR-27a plays an important role in ovarian cancer cell growth and metastasis, and genistein, as nontoxic inactivators of miRNA, can block ovarian cancer cell growth and migration, offering novel insights into the mechanisms of genistein therapeutic actions.


荷兰《药物化学中的抗癌药物》,
20139

在卵巢癌细胞中致癌的 MicroRNA-27a 是金雀异黄素的标靶

徐琳琳,向晶莹,沈建,等

中国江苏南京医科大学药理学院

microRNAs (miRNAs) 正在成为癌症中多种病理过程的重要调节因子。金雀异黄素,作为大豆分离的主要异黄酮,具有多种生物活性,特别是在癌症预防方面。然而,金雀异黄素影响卵巢癌细胞的分子机制尚未完全阐明。在此研究中,我们报道的miR-27a在人体卵巢癌中的表达比良性卵巢组织高。同时,SKOV3 细胞的基因转染,伴随着抑制剂 miR-27a抑制肿瘤细胞的增殖和迁移。我们的研究还发现用金雀异黄素治疗卵巢癌细胞抑制卵巢癌细胞的生长和迁移。进一步细胞机理研究揭示金雀异黄素下调了 miR-27a 表达,伴随着Sprouty2(一种公认的miR-27a的靶向基因)的表达显著增加。两者合计,我们的研究结果揭示了致癌因子 miR-27a 在卵巢癌细胞生长和转移方面的重要作用,并且金雀异黄素,作为miRNA无毒的灭活剂,可以阻止卵巢癌细胞的生长和迁移,为金雀异黄素治疗活性的机制提供新的见解。
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