Suppr超能文献

盾叶薯蓣中分离得到的盾叶新苷通过诱导线粒体凋亡和抑制 Akt 和丝裂原活化蛋白激酶信号通路抑制癌细胞生长。

Deltonin isolated from Dioscorea zingiberensis inhibits cancer cell growth through inducing mitochondrial apoptosis and suppressing Akt and mitogen activated protein kinase signals.

机构信息

Laboratory of Ethnopharmacology, Regenerative Medicine Research Center, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Gaoxinqu, Chengdu 610041, China.

出版信息

Biol Pharm Bull. 2011;34(8):1231-9. doi: 10.1248/bpb.34.1231.

Abstract

Deltonin is an active component purified from Dioscorea zingiberensis WRIGHT (DZW), and has shown anticancer effects. However, its mechanism of action remains elusive. In the present study, we investigated the effect of Deltonin on a panel of cancer cell lines and analyzed its mechanism in C26 cells, a murine colon carcinoma cell. Our results showed that Deltonin markedly inhibited the growth of all examined cancer cell lines. Deltonin induced dose- and time-dependent apoptosis in C26 cells. The event of apoptosis was accompanied by the release of cytochrome c, depolarization of mitochondrial membrane potential, and dose- and time-dependent reactive oxygen species (ROS) generation. Deltonin also increased the expression of Bax, decreased the expression of B-cell lymphoma/lewkmia-2 (Bcl-2), and induced the activation of caspase 9, caspase 3 and poly(ADP-ribose) polymerase (PARP). Furthermore, Deltonin decreased Akt and extracellular signal-regulated kinase-1/2 (ERK(1/2)) activity. These results demonstrate that Deltonin mediates the growth inhibition of cancer cells through multiple targets, which include the generation of reactive oxygen species (ROS), mitochondrial apoptosis and the inhibition of the mitogen-activated protein kinase (MAPK) and Akt signaling pathways, suggesting Deltonin is a potent cancer preventive and therapeutic agent.

摘要

丹皮灵是从盾叶薯蓣(DZW)中纯化得到的一种活性成分,具有抗癌作用。然而,其作用机制尚不清楚。在本研究中,我们研究了丹皮灵对一系列癌细胞系的影响,并在 C26 细胞(一种鼠结肠癌细胞)中分析了其作用机制。结果表明,丹皮灵明显抑制了所有检测到的癌细胞系的生长。丹皮灵诱导 C26 细胞呈剂量和时间依赖性凋亡。凋亡事件伴随着细胞色素 c 的释放、线粒体膜电位去极化以及剂量和时间依赖性活性氧(ROS)的产生。丹皮灵还增加了 Bax 的表达,降低了 B 细胞淋巴瘤/白血病-2(Bcl-2)的表达,并诱导了半胱天冬酶 9、半胱天冬酶 3 和多聚(ADP-核糖)聚合酶(PARP)的激活。此外,丹皮灵还降低了 Akt 和细胞外信号调节激酶-1/2(ERK(1/2))的活性。这些结果表明,丹皮灵通过多种靶点介导癌细胞的生长抑制,包括活性氧(ROS)的产生、线粒体凋亡以及丝裂原活化蛋白激酶(MAPK)和 Akt 信号通路的抑制,提示丹皮灵是一种有效的癌症预防和治疗剂。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验