Department of Pharmacognosy and Phytochemistry, Meiji Pharmaceutical University , Noshio 2-522-1 Kiyose-shi, Tokyo 204-8588, Japan.
J Nat Prod. 2014 Apr 25;77(4):1065-8. doi: 10.1021/np400687y. Epub 2014 Mar 4.
Hypoxylonol C (1), isolated from the inedible mushroom Hypoxylon truncatum, exhibited inhibitory activities against the migration and tube formation of HUVECs. A cDNA microarray analysis was performed to investigate the target of hypoxylonol C (1) in HUVECs, and it was found that the genes related to cell cycle and adhesion were down-regulated. The down-regulation of mRNA levels of cell cycle and adhesion genes was confirmed by real-time RT-PCR. Cell cycle arrest and suppression of adhesion molecule expression might be plausible mechanisms of actions for the antiangiogenic activity of hypoxylonol C (1).
Hypoxylonol C(1)从不可食用的蘑菇 Hypoxylon truncatum 中分离出来,表现出对 HUVECs 迁移和管形成的抑制活性。进行了 cDNA 微阵列分析,以研究 Hypoxylonol C(1)在 HUVECs 中的靶标,结果发现与细胞周期和黏附相关的基因下调。通过实时 RT-PCR 证实了细胞周期和黏附基因的 mRNA 水平下调。细胞周期停滞和黏附分子表达的抑制可能是 Hypoxylonol C(1)抗血管生成活性的合理作用机制。