Huang Xuedan, Awano Yurika, Maeda Eri, Asada Yoshihisa, Takemoto Hiroaki, Watanabe Takashi, Kojima-Yuasa Akiko, Kobayashi Yoshinori
a School of Pharmaceutical Sciences, Kitasato University , 5-9-1 Shirokane, Minato-ku , Tokyo 108-0086 , Japan.
Nat Prod Res. 2014;28(12):914-6. doi: 10.1080/14786419.2014.889133. Epub 2014 Mar 3.
In this study, we found that two sesquiterpene lactones, isobutyroylplenolin and arnicolide D, from Centipeda minima L. (Compositae) exerted stronger cytotoxic activity than cisplatin on the human colon carcinoma HT-29 cell line. Furthermore, the cytotoxicity of these two compounds on normal cells was weaker than that of cisplatin. Treatment with isobutyroylplenolin and arnicolide D increased the levels of intracellular reactive oxygen species and decreased the levels of nuclear factor-κB protein, resulting in cell cycle arrest in G1 phase and apoptosis. We also discuss the difference in structure and activity between these two compounds.
在本研究中,我们发现来自菊科植物小蓟的两种倍半萜内酯,异丁酰基蒲勒醇和紫菀内酯D,对人结肠癌HT-29细胞系的细胞毒性活性比顺铂更强。此外,这两种化合物对正常细胞的细胞毒性比顺铂弱。用异丁酰基蒲勒醇和紫菀内酯D处理会增加细胞内活性氧的水平,并降低核因子-κB蛋白的水平,导致细胞周期停滞在G1期并诱导凋亡。我们还讨论了这两种化合物在结构和活性上的差异。