Kim Eun-Ji, Kang Jung Il, Tung Nguyen-Huu, Kim Young-Ho, Hyun Jin Won, Koh Young Sang, Chang Weon-Young, Yoo Eun Sook, Kang Hee-Kyoung
School of Medicine, Jeju National University, Jeju 63243, Republic of Korea.
College of Pharmacy, Chungnam National University, Daejeon 34134, Republic of Korea.
Biomol Ther (Seoul). 2016 Nov 1;24(6):623-629. doi: 10.4062/biomolther.2016.023.
(1S,2S,3E,7E,11E)-3,7,11,15-cembratetraen-17,2-olide (LS-1), a marine cembrenolide diterpene, has anticancer activity against colon cancer cells such as HT-29, SNU-C5/5-FU (fluorouracil-resistant SNU-C5) and SNU-C5. However, the action mechanism of LS-1 on SNU-C5 human colon cancer cells has not been fully elucidated. In this study, we investigated whether the anticancer effect of LS-1could result from apoptosis via the modulation of Wnt/β-catenin and the TGF-β pathways. When treated with the LS-1, we could observe the apoptotic characteristics such as apoptotic bodies and the increase of sub-G1 hypodiploid cell population, increase of Bax level, decrease of Bcl-2 expression, cleavage of procaspase-3 and cleavage of poly (ADP-ribose) polymerase in SNU-C5 cells. Furthermore, the apoptosis induction of SNU-C5 cells upon LS-1 treatment was also accompanied by the down-regulation of Wnt/β-catenin signaling pathway via the decrease of GSK-3β phosphorylation followed by the decrease of β-catenin level. In addition, the LS-1 induced the activation of TGF-β signaling pathway with the decrease of carcinoembryonic antigen which leads to decrease of c-Myc, an oncoprotein. These data suggest that the LS-1 could induce the apoptosis via the down-regulation of Wnt/β-catenin pathway and the activation of TGF-β pathway in SNU-C5 human colon cancer cells. The results support that the LS-1 might have potential for the treatment of human colon cancer.
(1S,2S,3E,7E,11E)-3,7,11,15-西松烯四烯-17,2-内酯(LS-1)是一种海洋西松烯内酯二萜,对结肠癌细胞如HT-29、SNU-C5/5-FU(氟尿嘧啶耐药的SNU-C5)和SNU-C5具有抗癌活性。然而,LS-1对SNU-C5人结肠癌细胞的作用机制尚未完全阐明。在本研究中,我们研究了LS-1的抗癌作用是否可能通过调节Wnt/β-连环蛋白和TGF-β信号通路导致细胞凋亡。用LS-1处理后,我们可以观察到SNU-C5细胞中的凋亡特征,如凋亡小体和亚G1期亚二倍体细胞群增加、Bax水平升高、Bcl-2表达降低、procaspase-3裂解以及聚(ADP-核糖)聚合酶裂解。此外,LS-1处理后SNU-C5细胞的凋亡诱导还伴随着Wnt/β-连环蛋白信号通路的下调,这是通过GSK-3β磷酸化的降低以及随后β-连环蛋白水平的降低实现的。此外,LS-1诱导TGF-β信号通路的激活,同时癌胚抗原减少,这导致癌蛋白c-Myc减少。这些数据表明,LS-1可通过下调SNU-C5人结肠癌细胞中的Wnt/β-连环蛋白通路和激活TGF-β通路诱导细胞凋亡。结果支持LS-1可能具有治疗人类结肠癌的潜力。