Sanggenon C Suppresses Tumorigenesis of Gastric Cancer by Blocking ERK-Drp1-Mediated Mitochondrial Fission.
Xiao-Jie ChenQi-Xiao CuiGuo-Li WangXiao-Li LiXiao-Lin ZhouHui-Jie ZhaoMing-Qian ZhangMin-Jing LiXiao-Juan HeQiu-Sheng ZhengYu-Liang WangDe-Fang LiPan HongPublished in: Journal of natural products (2022)
Sanggenon C is a flavonoid extracted from the root bark of white mulberry, which is a traditional Chinese medicine with anti-inflammatory, antioxidative, and antitumor pharmacological effects. In this study, sanggenon C was found to inhibit human gastric cancer (GC) cell proliferation and colony formation, induce GC cell cycle arrest in the G0-G1 phase, and promote GC cell apoptosis. Moreover, sanggenon C was found to decrease the level of mitochondrial membrane potential in GC cells and inhibit mitochondrial fission. Mechanistically, RNA sequencing, bioinformatics analysis, and a series of functional analyses confirmed that sanggenon C inhibited mitochondrial fission to induce apoptosis by blocking the extracellular regulated protein kinases (ERK) signaling pathway, and constitutive activation of ERK significantly abrogated these effects. Finally, sanggenon C was found to suppress the growth of tumor xenografts in nude mice without obvious side effects to the vital organs of animals. This study reveals that sanggenon C could be a novel therapeutic strategy for GC treatment.
Keyphrases
- endothelial cells
- cell cycle arrest
- pi k akt
- signaling pathway
- cell proliferation
- oxidative stress
- induced apoptosis
- cell death
- anti inflammatory
- gas chromatography
- epithelial mesenchymal transition
- bioinformatics analysis
- type diabetes
- single cell
- cell cycle
- transcription factor
- risk assessment
- climate change
- mass spectrometry
- combination therapy
- replacement therapy
- induced pluripotent stem cells