Liu Bin, Zhang Miaomiao, Liu Shuna, Ying Jie, Zhang Jingjing, Kurihara Hiroshi, Zheng Weiqiang, He Rong-Rong, Zhu Runzhi
Infection department of Internal Medicine, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong Province. China.
Clinical Research Center. China.
Protein Pept Lett. 2017;24(5):413-418. doi: 10.2174/0929866524666170223094634.
Diosmetin (Dios), a flavone aglycone, is a major active ingredient of many herbal medicines. Previous studies implicated that the potential antitumor activities of Dios are mediated through multiple cell signaling pathways, however more investigations are required to reveal the targets and mechanisms of Dios. In this study, our results demonstrated that cell cycle progression and proliferation of HepG2 cells were inhibited by Dios. Meanwhile, Dios-induced liver cancer cell apoptosis was related with the p53 activation. After PFT-α, a p53 inhibitor was added into Dios-treated HepG2 cells, cell growth inhibition was partially reversed. These findings defined and supported that p53 is a novel target of Dios. By activating p53, Dios exerts anticancer effects by inducing cell cycle arrest and apoptosis in HepG2 cells.
香叶木素(Dios)是一种黄酮苷元,是许多草药的主要活性成分。先前的研究表明,香叶木素的潜在抗肿瘤活性是通过多种细胞信号通路介导的,然而,还需要更多的研究来揭示香叶木素的靶点和作用机制。在本研究中,我们的结果表明香叶木素可抑制HepG2细胞的细胞周期进程和增殖。同时,香叶木素诱导的肝癌细胞凋亡与p53激活有关。在将p53抑制剂PFT-α加入经香叶木素处理的HepG2细胞后,细胞生长抑制得到部分逆转。这些发现明确并支持p53是香叶木素的一个新靶点。通过激活p53,香叶木素通过诱导HepG2细胞的细胞周期停滞和凋亡发挥抗癌作用。