首页> 外文期刊>Anti-cancer drugs >Tanshinone IIA induces apoptosis and inhibits the proliferation, migration, and invasion of the osteosarcoma MG-63 cell line in vitro.
【24h】

Tanshinone IIA induces apoptosis and inhibits the proliferation, migration, and invasion of the osteosarcoma MG-63 cell line in vitro.

机译:丹参酮IIA在体外可诱导细胞凋亡并抑制骨肉瘤MG-63细胞系的增殖,迁移和侵袭。

获取原文
获取原文并翻译 | 示例
           

摘要

Tanshinone IIA (Tan IIA) is an active ingredient extracted from the widely used Danshen root (Salvia miltiorrhiza Bunge), a traditional Chinese medicine. Recent studies have indicated that Tan IIA may play important roles in anticancer treatment. However, its effects on the most common primary malignant bone tumor, osteosarcoma (OS), are unknown. Here, we report that Tan IIA may be an efficacious anti-OS drug as it could induce cell apoptosis and inhibit proliferation, migration, and invasion in vitro. Furthermore, we detected possible molecular mechanisms for Tan IIA activity by examining the levels of Bcl-2, Bax expression, and caspase-3, caspase-8, and caspase-9 activities that regulate apoptosis, matrix metalloproteinase (MMP)-2, and MMP-9 involved in regulating migration and invasion. In this study, we find that Tan IIA inhibits proliferation and induces apoptosis in the human OS cell line MG-63 in a time-dependent and dose-dependent manner. In addition, Tan IIA displays inhibitory activity on OS cell migration and invasion. Mechanistic studies have shown that Tan IIA activity is mediated by caspase activation. Tan IIA was also shown to reduce antiapoptotic Bcl-2, MMP-2, and MMP-9 levels, whereas it increased proapoptotic Bax levels. These data suggest that Tan IIA may be a novel, efficient candidate agent for OS treatment.
机译:丹参酮IIA(Tan IIA)是从广泛使用的中药丹参根(Salvia miltiorrhiza Bunge)中提取的有效成分。最近的研究表明,Tan IIA可能在抗癌治疗中起重要作用。但是,其对最常见的原发性恶性骨肿瘤骨肉瘤(OS)的作用尚不清楚。在这里,我们报道Tan IIA可能是一种有效的抗OS药物,因为它可以诱导细胞凋亡并抑制体外增殖,迁移和侵袭。此外,我们通过检查Bcl-2,Bax表达以及调节凋亡,基质金属蛋白酶(MMP)-2和Caspase-3,caspase-8和caspase-9活性的水平来检测Tan IIA活性的可能分子机制。 MMP-9参与调节迁移和入侵。在这项研究中,我们发现Tan IIA以时间依赖性和剂量依赖性方式抑制人OS细胞系MG-63的增殖并诱导其凋亡。另外,Tan IIA对OS细胞的迁移和侵袭显示出抑制活性。机理研究表明,Tan IIA活性是由caspase激活介导的。 Tan IIA还显示可以降低抗凋亡的Bcl-2,MMP-2和MMP-9水平,而它可以增加促凋亡的Bax水平。这些数据表明,Tan IIA可能是OS治疗的新型有效候选药物。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号