Department of Nutrition and Health Sciences, Chang Gung Institute of Technology, Taoyuan 333, Taiwan.
J Agric Food Chem. 2011 Mar 23;59(6):2347-55. doi: 10.1021/jf105003n. Epub 2011 Feb 18.
The Tithonia diversifolia methanolic extract (TDM), which showed antiproliferative activity against human glioblastoma U373 cells, with an IC50 value of 59.2±3.7 μg mL(-1), was passed through silica gel chromatography and successively eluted with different percentages of EtOAc/hexane. The 10-60% EtOAc/hexane subfractions, which exhibited a comparatively higher antiproliferative activity, were isolated, and then structural identification was proceeded with 1H nuclear magnetic resonance. The isolated compound was tagitinin C, a kind of sesquiterpenoid. The IC50 value was 6.1±0.1 μg mL(-1) in U373 treated with tagitinin C. In flow cytometric analysis and inhibition of pan-caspase, the results showed that the anti-glioblastoma effect was apoptosis-independent. In PARP, p-p38, ULK1, and LC3-II expression, the anti-glioblastoma induced by tagitinin C was likely via autophagy. In the ULK1 siRNA transfection experiment, autophagy blockade counteracted the suppression induced by tagitinin C. The result suggested that tagitinin C induces U373 cell death dependent upon autophagy under certain conditions.
黄花稔的甲醇提取物(TDM)对人神经胶质瘤 U373 细胞表现出抗增殖活性,IC50 值为 59.2±3.7μg/mL,经硅胶柱层析分离,用不同比例的 EtOAc/hexane 洗脱,分离出的具有相对较高的抗增殖活性的 10-60% EtOAc/hexane 级分,并用 1H 核磁共振进行了结构鉴定。分离得到的化合物是 tagitinin C,一种倍半萜烯。Tagitinin C 处理 U373 细胞的 IC50 值为 6.1±0.1μg/mL。在流式细胞术分析和广谱半胱天冬酶抑制剂实验中,结果表明 tagitinin C 的抗神经胶质瘤作用与细胞凋亡无关。在 PARP、p-p38、ULK1 和 LC3-II 的表达中,tagitinin C 诱导的抗神经胶质瘤作用可能是通过自噬实现的。在 ULK1 siRNA 转染实验中,自噬阻断逆转了 tagitinin C 诱导的抑制作用。结果表明,在某些条件下,tagitinin C 诱导 U373 细胞死亡依赖于自噬。