Hou Xinrui, Zhang Zhendong, Cao Mingyuan, DU Yuxin, Wang Xiaoping
School of Medicine, Xizang Minzu University, Xianyang 712082, China.
Key Laboratory of High Altitude Hypoxia Environment and Life Health, Xizang Minzu University, Xianyang 712082, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2025 Jun 20;45(6):1226-1239. doi: 10.12122/j.issn.1673-4254.2025.06.12.
To investigate the mechanism through which salidroside inhibits proliferation of gastric cancer (GC) cells focusing on glucose metabolic reprogramming pathways.
High-throughput sequencing combined with bioinformatics analysis was employed to identify the potential targets of salidroside in human GC MGC-803 cells. Liposome-mediated transfection experiments were carried out to validate the functional and mechanistic roles of these targets. CCK-8 and colony formation assays were used to assess the effects of salidroside on GC cell viability and clonogenic ability. qRT-PCR, Western blotting, and biochemical assay kits were used to analyze the regulatory effects of salidroside on the miR-1343-3p-OGDHL/PDHB enzyme complex-pyruvate metabolic pathway in GC cells.
Bioinformatics analysis suggested that the tumor-suppressive factor miR-1343-3p negatively regulated the key glycolytic enzyme gene oxoglutarate dehydrogenase-like (OGDHL) in GC cells, and OGDHL and pyruvate dehydrogenase E1 subunit beta (PDHB) were both significantly upregulated in GC tissues, which was close by correlated with reduced survival rates of GC patients. In MGC-803 cells, salidroside treatment significantly enhanced the expression level of miR-1343-3p and downregulated OGDHL expression, resulting in disruption of the stability of PDHB, reduced pyruvate oxidative decarboxylation, and consequently decreased production of acetyl-CoA and ATP.
Salidroside inhibits GC cell proliferation possibly by regulating the miR-1343-3p-OGDHL/PDHB enzyme complex-pyruvate metabolic pathway, which provides new insights into its anti-tumor mechanisms and suggests new strategies for targeted therapy for GC.
以葡萄糖代谢重编程途径为重点,研究红景天苷抑制胃癌(GC)细胞增殖的机制。
采用高通量测序结合生物信息学分析,鉴定红景天苷在人GC MGC-803细胞中的潜在靶点。进行脂质体介导的转染实验,以验证这些靶点的功能和机制作用。使用CCK-8和集落形成试验评估红景天苷对GC细胞活力和克隆形成能力的影响。采用qRT-PCR、蛋白质免疫印迹法和生化检测试剂盒分析红景天苷对GC细胞中miR-1343-3p-OGDHL/PDHB酶复合物-丙酮酸代谢途径的调控作用。
生物信息学分析表明,肿瘤抑制因子miR-1343-3p负向调控GC细胞中关键糖酵解酶基因氧代戊二酸脱氢酶样(OGDHL),且OGDHL和丙酮酸脱氢酶E1亚基β(PDHB)在GC组织中均显著上调,这与GC患者生存率降低密切相关。在MGC-803细胞中,红景天苷处理显著提高miR-1343-3p的表达水平并下调OGDHL表达,导致PDHB稳定性破坏,丙酮酸氧化脱羧减少,从而使乙酰辅酶A和ATP生成减少。
红景天苷可能通过调节miR-1343-3p-OGDHL/PDHB酶复合物-丙酮酸代谢途径抑制GC细胞增殖,这为其抗肿瘤机制提供了新见解,并为GC的靶向治疗提出了新策略。