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野生苦荬菜提取物通过 p53 介导的 ATM/Fas 信号通路激活内、外源性途径诱导人结直肠癌细胞 HCT116 凋亡

Activations of Both Extrinsic and Intrinsic Pathways in HCT 116 Human Colorectal Cancer Cells Contribute to Apoptosis through p53-Mediated ATM/Fas Signaling by Emilia sonchifolia Extract, a Folklore Medicinal Plant.

机构信息

School of Pharmacy, China Medical University, Taichung 404, Taiwan.

出版信息

Evid Based Complement Alternat Med. 2012;2012:178178. doi: 10.1155/2012/178178. Epub 2012 Feb 28.

Abstract

Emilia sonchifolia (L.) DC (Compositae), an herbaceous plant found in Taiwan and India, is used as folk medicine. The clinical applications include inflammation, rheumatism, cough, cuts fever, dysentery, analgesic, and antibacteria. The activities of Emilia sonchifolia extract (ESE) on colorectal cancer cell death have not been fully investigated. The purpose of this study explored the induction of apoptosis and its molecular mechanisms in ESE-treated HCT 116 human colorectal cancer cells in vitro. The methanolic ESE was characterized, and γ-humulene was formed as the major constituent (63.86%). ESE induced cell growth inhibition in a concentration- and time-dependent response by MTT assay. Apoptotic cells (DNA fragmentation, an apoptotic catachrestic) were found after ESE treatment by TUNEL assay and DNA gel electrophoresis. Alternatively, ESE stimulated the activities of caspase-3, -8, and -9 and their specific caspase inhibitors protected against ESE-induced cytotoxicity. ESE promoted the mitochondria-dependent and death-receptor-associated protein levels. Also, ESE increased ROS production and upregulated the levels of ATM, p53, and Fas in HCT 116 cells. Strikingly, p53 siRNA reversed ESE-reduced viability involved in p53-mediated ATM/Fas signaling in HCT 116 cells. In summary, our result is the first report suggesting that ESE may be potentially efficacious in the treatment of colorectal cancer.

摘要

台湾和印度产的菊科植物长茎飞蓬(Emilia sonchifolia(L.)DC),被用作民间药物。其临床应用包括炎症、风湿、咳嗽、发热、痢疾、止痛和抗菌。长茎飞蓬提取物(ESE)对结直肠癌细胞死亡的作用尚未得到充分研究。本研究旨在探讨 ESE 体外处理人结直肠癌细胞 HCT 116 诱导细胞凋亡及其分子机制。甲醇提取物 ESE 的特征是γ-葎草烯为主要成分(63.86%)。MTT 试验结果显示 ESE 呈浓度和时间依赖性抑制细胞生长。TUNEL 试验和 DNA 凝胶电泳显示 ESE 处理后出现凋亡细胞(DNA 片段化,凋亡特征)。另外,ESE 刺激了 caspase-3、-8 和 -9 的活性,其特异性半胱天冬酶抑制剂可防止 ESE 诱导的细胞毒性。ESE 促进了线粒体依赖性和死亡受体相关蛋白水平的增加。ESE 还增加了 ROS 的产生并上调了 HCT 116 细胞中 ATM、p53 和 Fas 的水平。值得注意的是,p53 siRNA 逆转了 ESE 降低的活力,涉及 p53 介导的 ATM/Fas 信号通路在 HCT 116 细胞中的作用。总之,我们的结果首次表明,ESE 可能在结直肠癌的治疗中具有潜在疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0763/3303801/30a8499ad02e/ECAM2012-178178.001.jpg

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