Yao Chunping, Cao Xiujuan, Fu Zheng, Tian Jing, Dong Wei, Xu Jin, An Kang, Zhai Limin, Yu Jinming
Department of Radiation Oncology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China (mainland).
Department of Radiation Oncology, Shandong Cancer Hospital Affiliated with Shandong University, Shandong Academy of Medical Science, Jinan, Shandong, China (mainland).
Med Sci Monit. 2017 Apr 29;23:2059-2064. doi: 10.12659/msm.901381.
BACKGROUND Laryngeal cancer is a malignant head and neck tumor with high morbidity and high mortality in humans. Recently, treatments with Chinese medicines and their extracts have gradually received great attention, and studies suggest that Boschniakia rossica polysaccharide (BRP) has potential anti-tumor activity. Therefore, this study investigating the role of BRP in inducing apoptosis in human laryngeal carcinoma cells. MATERIAL AND METHODS The BRP was extracted with organic solvent and HR column. We treated Hep2 laryngeal carcinoma cells with different concentrations of BRP, then assessed cell growth inhibition rate by flow cytometry and apoptosis index by TUNEL staining. The protein expression of p53, Bcl-2, Bax, and caspase-3 were analyzed by Western blot. RESULTS Flow cytometry results showed that BRP inhibited Hep2 cell proliferation in a dose-dependent manner (p<0.05), and TUNEL staining indicated that BRP significantly increased Hep2 apoptosis index (p<0.05). Western blot results showed that the expression levels of p53 and activation of caspase-3 in Hep2 cells were significantly up-regulated (p<0.05), while the expression of Bcl-2 was significantly down-regulated (p<0.05). CONCLUSIONS BRP might induce cell apoptosis by regulating the expression level of cell apoptosis-associated proteins, suggesting strong anti-laryngeal cancer activity.
背景 喉癌是一种人类发病率和死亡率都很高的头颈部恶性肿瘤。近年来,中药及其提取物的治疗方法逐渐受到广泛关注,研究表明红景天多糖(BRP)具有潜在的抗肿瘤活性。因此,本研究旨在探讨BRP在诱导人喉癌细胞凋亡中的作用。
材料与方法 采用有机溶剂和HR柱提取BRP。用不同浓度的BRP处理Hep2喉癌细胞,然后通过流式细胞术评估细胞生长抑制率,通过TUNEL染色评估凋亡指数。通过蛋白质免疫印迹法分析p53、Bcl-2、Bax和caspase-3的蛋白表达。
结果 流式细胞术结果显示,BRP以剂量依赖性方式抑制Hep2细胞增殖(p<0.05),TUNEL染色表明BRP显著增加Hep2细胞凋亡指数(p<0.05)。蛋白质免疫印迹法结果显示,Hep2细胞中p53的表达水平和caspase-3的激活显著上调(p<0.05),而Bcl-2的表达显著下调(p<0.05)。
结论 BRP可能通过调节细胞凋亡相关蛋白的表达水平诱导细胞凋亡,提示其具有较强的抗喉癌活性。