Lv Yifei, Li Changshun, Li Shuang, Hao Zhiming
Department of Gastroenterology, The First Affiliated Hospital, College of Medicine, Xi'an Jiaotong University, Xi'an 710061, P.R. China.
Oncol Lett. 2011 Jul;2(4):741-745. doi: 10.3892/ol.2011.305. Epub 2011 May 13.
Sinomenine (SIN) is a bioactive alkaloid extracted from the Chinese medicinal plant Sinomenium acutum. Results of studies have shown that the anti-inflammatory, immunosuppressive and anti-arthritic effects of SIN are partially attributed to the inhibition of cyclooxygenase-2 (COX-2) expression. COX-2 overexpression is associated with enhanced proliferation and angiogenesis of gastric cancer (GC). SGC-7901 cells were treated with different concentrations of SIN in order to observe its effect on the proliferation of human gastric adenocarcinoma cells and to explore the potential underlying molecular mechanism via the detection of COX-2 expression. Celecoxib was used as the positive control. Morphological alterations of the cells were observed microscopically. Cell proliferation was evaluated using MTT assay. COX-2 expression was detected using semi-quantitative RT-PCR and Western blotting. The results showed that SIN inhibited the proliferation of SGC-7901 cells in a time- and dose-dependent manner. In the presence of SIN or celecoxib, SGC-7901 cells became round and detached morphologically, indicating cell apoptosis. The expression of COX-2 was inhibited by SIN in a dose-dependent manner at both the mRNA and protein levels. Our findings indicate that the protective effects of SIN are mediated through the inhibition of COX-2 expression. These findings suggest a novel therapy to treat inflammation-mediated gastric adenocarcinomata.
青藤碱(SIN)是从中国药用植物青风藤中提取的一种生物活性生物碱。研究结果表明,SIN的抗炎、免疫抑制和抗关节炎作用部分归因于其对环氧化酶-2(COX-2)表达的抑制。COX-2的过度表达与胃癌(GC)的增殖和血管生成增强有关。用不同浓度的SIN处理SGC-7901细胞,以观察其对人胃腺癌细胞增殖的影响,并通过检测COX-2表达来探索潜在的分子机制。塞来昔布用作阳性对照。显微镜下观察细胞的形态变化。使用MTT法评估细胞增殖。使用半定量RT-PCR和蛋白质印迹法检测COX-2表达。结果表明,SIN以时间和剂量依赖性方式抑制SGC-7901细胞的增殖。在存在SIN或塞来昔布的情况下,SGC-7901细胞在形态上变得圆形并脱离,表明细胞凋亡。SIN在mRNA和蛋白质水平上均以剂量依赖性方式抑制COX-2的表达。我们的研究结果表明,SIN的保护作用是通过抑制COX-2表达介导的。这些发现提示了一种治疗炎症介导的胃腺癌的新疗法。