a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
b Microbiology Department, Faculty of Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
Nutr Cancer. 2019;71(1):159-171. doi: 10.1080/01635581.2018.1540719. Epub 2019 Jan 16.
The current study explored the basic molecular mechanisms of zerumbone (ZER), an herbal compound, in inhibiting the migration and invasion of colorectal cancer (CRC) cells in vitro. Two types of CRC cells, namely HCT-116 and SW48, were treated with various concentrations of ZER (8, 16, and 24 µM) for 24, 48, and 72 h, respectively. In vitro assays were performed to determine alterations in proliferation ability, mRNA expression and protein levels, and migration and invasion potential of CRC cells. An SYBR Green-based quantitative polymerase chain reaction (PCR) was utilized to detect the gene expression of focal adhesion kinase (FAK), nuclear factor (NF)-κB, and urokinase-type plasminogen activator (uPA) followed by the evaluation of the level of proteins by western blotting. Migration and invasion potentials of HCT-116 and SW48 cells treated by ZER were examined using migration and invasion assay kits, respectively. We compared the results of all experiments with control groups, including FAK inhibitor, ZER + FAK inhibitor-treated cells, NF-β inhibitor, ZER + NF-β inhibitor, and untreated cells. The data in the present study suggest that ZER may exert its antimetastatic effects through inhibition of FAk/PI3k/NF-κB-uPA signaling pathway, thereby possibly representing a novel class of FAK inhibitors.
本研究探讨了姜烯(ZER)这种草药化合物在体外抑制结直肠癌(CRC)细胞迁移和侵袭的基本分子机制。两种类型的 CRC 细胞,即 HCT-116 和 SW48,分别用不同浓度的 ZER(8、16 和 24μM)处理 24、48 和 72 小时。进行了体外试验以确定 CRC 细胞增殖能力、mRNA 表达和蛋白水平以及迁移和侵袭潜力的变化。采用 SYBR Green 定量聚合酶链反应(PCR)检测粘着斑激酶(FAK)、核因子(NF)-κB 和尿激酶型纤溶酶原激活物(uPA)的基因表达,然后通过蛋白质印迹法评估蛋白水平。分别使用迁移和侵袭试验试剂盒检测 ZER 处理的 HCT-116 和 SW48 细胞的迁移和侵袭潜力。我们将所有实验的结果与对照组进行比较,包括 FAK 抑制剂、ZER+FAK 抑制剂处理的细胞、NF-β 抑制剂、ZER+NF-β 抑制剂和未处理的细胞。本研究的数据表明,ZER 可能通过抑制 FAk/PI3k/NF-κB-uPA 信号通路发挥其抗转移作用,因此可能代表一类新型的 FAK 抑制剂。