Schisandrin B exerts anticancer effects on human gastric cancer cells through ROS-mediated MAPK, STAT3, and NF-κB pathways

[摘要] Schisandrin B (Sch B) is a monomer with anti-cancer and anti-inflammatory effects, which are isolated from theplant Schisandra chinensis (Turcz) Baillon. We investigated the anti-gastric cancer (GC) effects of Sch B and itsunderlying molecular mechanisms. The Cell Counting Kit-8 assay was used to determine the effects of Sch B on theviability of GC and normal cell lines. Hoechst/propidium iodide staining and flow cytometry were used to assess theapoptosis induction of Sch B. Western blotting was used to evaluate the effects of Sch B on downstream apoptoticproteins. The DCFH-DA fluorescent probe was used to assess the regulatory effects of Sch B on reactive oxygenspecies (ROS) levels and related signaling pathways in GC cells. The results showed that Sch B could regulate thephosphorylation level of mitogen-activated protein kinase (MAPK) by upregulating ROS accumulation in gastriccancer cells, and then reduce the expression of nuclear factor kappa B (NF-κB) and phosphorylated transcription3 (p-STAT3). In addition, Sch B downregulated the cell cycle proteins cyclin-dependent kinase 2/4/6 and cyclin D1/E,and arrested cells in the G0/G1 phase. Moreover, it also inhibited cell migration, which was reversed with Nacetylcysteine pretreatment. In summary, Sch B has killing effects on GC cells by upregulating the production ofintracellular ROS and regulating the MAPK/STAT3/NF-κB signaling pathway, leading to the migration arrest andapoptosis of GC cells.

[学科分类] 仪器

[关键词] Schisandrin B;Gastric cancer;Reactive oxygen species;Apoptosis;Migration;Cell cycle