Suppr超能文献

红松叶精油通过 ROS 生成和半胱天冬酶的激活诱导 YD-8 人口腔癌细胞凋亡。

Pinus densiflora leaf essential oil induces apoptosis via ROS generation and activation of caspases in YD-8 human oral cancer cells.

机构信息

Department of Medical Genetic Engineering, Keimyung University School of Medicine, Daegu 704-701, Republic of Korea.

出版信息

Int J Oncol. 2012 Apr;40(4):1238-45. doi: 10.3892/ijo.2011.1263. Epub 2011 Nov 11.

Abstract

The leaf of Pinus (P.) densiflora, a pine tree widely distributed in Asian countries, has been used as a traditional medicine. In the present study, we investigated the anticancer activity of essential oil, extracted by steam distillation, from the leaf of P. densiflora in YD-8 human oral squamous cell carcinoma (OSCC) cells. Treatment of YD-8 cells with P. densiflora leaf essential oil (PLEO) at 60 µg/ml for 8 h strongly inhibited proliferation and survival and induced apoptosis. Notably, treatment with PLEO led to generation of ROS, activation of caspase-9, PARP cleavage, down-regulation of Bcl-2, and phosphorylation of ERK-1/2 and JNK-1/2 in YD-8 cells. Treatment with PLEO, however, did not affect the expression of Bax, XIAP and GRP78. Importantly, pharmaco-logical inhibition studies demonstrated that treatment with vitamin E (an anti-oxidant) or z-VAD-fmk (a pan-caspase inhibitor), but not with PD98059 (an ERK-1/2 inhibitor) or SP600125 (a JNK-1/2 inhibitor), strongly suppressed PLEO-induced apoptosis in YD-8 cells and reduction of their survival. Vitamin E treatment further blocked activation of caspase-9 and Bcl-2 down-regulation induced by PLEO. Thus, these results demonstrate firstly that PLEO has anti-proliferative, anti-survival and pro-apoptotic effects on YD-8 cells and the effects are largely due to the ROS-dependent activation of caspases.

摘要

松叶(P.)densiflora 的叶子,一种广泛分布在亚洲国家的松树,已被用作传统药物。在本研究中,我们研究了从 P. densiflora 叶子中提取的精油对 YD-8 人口腔鳞状细胞癌(OSCC)细胞的抗癌活性。用 60μg/ml 的 P. densiflora 叶精油(PLEO)处理 YD-8 细胞 8 小时,强烈抑制增殖和存活,并诱导细胞凋亡。值得注意的是,PLEO 处理导致 ROS 的产生、caspase-9 的激活、PARP 切割、Bcl-2 的下调以及 ERK-1/2 和 JNK-1/2 的磷酸化。然而,PLEO 处理不影响 Bax、XIAP 和 GRP78 的表达。重要的是,药物抑制研究表明,用维生素 E(抗氧化剂)或 z-VAD-fmk(一种泛半胱天冬酶抑制剂)处理,但不用 PD98059(一种 ERK-1/2 抑制剂)或 SP600125(一种 JNK-1/2 抑制剂)处理,强烈抑制了 PLEO 诱导的 YD-8 细胞凋亡和存活减少。维生素 E 处理进一步阻断了 PLEO 诱导的 caspase-9 激活和 Bcl-2 下调。因此,这些结果表明,PLEO 对 YD-8 细胞具有抗增殖、抗存活和促凋亡作用,这些作用主要是由于 ROS 依赖性半胱天冬酶的激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d78/3584576/e4e8988bce95/IJO-40-04-1238-g00.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验