Chen Ling, Ruan Yuanyuan, Wang Xuefei, Min Lingqiang, Shen Zhenbin, Sun Yihong, Qin Xinyu
Department of General Surgery, Zhongshan Hospital, Fudan University, 180 Fenglin Road, Shanghai, 200032, People's Republic of China.
J Gastroenterol. 2014 May;49(5):864-74. doi: 10.1007/s00535-013-0848-4. Epub 2013 Jul 12.
Inhibitors of nuclear factor (NF)-κB pathway have shown potential anti-tumor activities. However, it is not fully elucidated in gastric cancer.
Firstly, we screened the inhibitory effect of pharmacologic NF-κB inhibitors on cell viability of human gastric cancer cells via CCK-8 assay. Next, cell apoptosis, cell cycle distribution, and mitochondrial membrane potential after BAY 11-7082 treatment were detected by annexin V staining, propidium iodide staining, TUNEL, and JC-1 assays in human gastric cancer HGC-27 cells. Expression of regulatory factors for apoptosis and cell cycle were measured by western blot. Finally, human gastric cancer xenograft model was established to verify the anti-tumor effects of BAY 11-7082 in vivo. Cellular apoptosis and growth inhibition in subcutaneous tumor section were detected by TUNEL and immunohistochemistry assays.
BAY 11-7082 exhibited rapid and potent anti-tumor effects on gastric cancer cells in vitro within a panel of NF-κB inhibitors. BAY 11-7082 induced rapid apoptosis in HGC-27 cells through activating the mitochondrial pathway, as well as down-regulation of Bcl-2 and up-regulation of Bax. BAY 11-7082 also induced S phase arrest through suppressing Cyclin A and CDK-2 expression. Xenograft model confirmed the anti-tumor effects of BAY 11-7082 on apoptosis induction and growth inhibition in vivo.
Our results demonstrated that BAY 11-7082 presented the most rapid and potent anti-tumor effects within a panel of NF-κB inhibitors, and could induce cellular apoptosis and block cell cycle progression both in vitro and in vivo, thus providing basis for clinical application of BAY 11-7082 in gastric cancer cases.
核因子(NF)-κB通路抑制剂已显示出潜在的抗肿瘤活性。然而,在胃癌中尚未完全阐明。
首先,我们通过CCK-8法筛选了药理学NF-κB抑制剂对人胃癌细胞活力的抑制作用。接下来,通过膜联蛋白V染色、碘化丙啶染色、TUNEL和JC-1法检测人胃癌HGC-27细胞经BAY 11-7082处理后的细胞凋亡、细胞周期分布和线粒体膜电位。通过蛋白质免疫印迹法检测凋亡和细胞周期调节因子的表达。最后,建立人胃癌异种移植模型以验证BAY 11-7082在体内的抗肿瘤作用。通过TUNEL和免疫组织化学法检测皮下肿瘤切片中的细胞凋亡和生长抑制情况。
在一组NF-κB抑制剂中,BAY 11-7082在体外对胃癌细胞表现出快速而有效的抗肿瘤作用。BAY 11-7082通过激活线粒体途径诱导HGC-27细胞快速凋亡,同时下调Bcl-2并上调Bax。BAY 11-7082还通过抑制细胞周期蛋白A和CDK-2的表达诱导S期阻滞。异种移植模型证实了BAY 11-7082在体内诱导凋亡和抑制生长的抗肿瘤作用。
我们的结果表明,在一组NF-κB抑制剂中,BAY 11-7082呈现出最快速而有效的抗肿瘤作用,并且在体外和体内均可诱导细胞凋亡并阻断细胞周期进程,从而为BAY 11-7082在胃癌病例中的临床应用提供了依据。