迷迭香酸/小檗碱无载体自组装纳米颗粒通过调节凋亡相关蛋白抑制卵巢癌细胞增殖与迁移OA
Rosmarinic acid/berberine carrier-free self-assembled nanoparticles(RBNPs)inhibits the proliferation and migration of ovarian cancer cells by regulating apoptosis-related proteins
目的:探讨自组装二元无载体纳米药物(RBNPs)在体外通过调节凋亡相关蛋白对卵巢癌细胞 SKOV3 和 CAOV3 增殖、迁移的影响及潜在分子机制.方法:选取 SK-OV3 和CAOV3 两种卵巢癌细胞系,通过CCK-8 法、克隆实验和划痕实验评估RBNPs 对细胞活力、增殖能力的影响;通过划痕实验、Transwell 实验评估 RBNPs 对细胞迁移能力的影响;利用蛋白质印迹法分析凋亡相关蛋白及 PI3K/AKT/mTOR 信号通路相关蛋白的表达.结果:CCK-8 检测显示 RBNPs 能减弱卵巢癌细胞活性,克隆形成实验表明 RBNPs 可显著抑制卵巢癌细胞增殖能力;划痕实验与Transwell 实验双重验证RBNPs 可显著抑制卵巢癌细胞迁移能力,排除了细胞增殖对实验结果的干扰;流式细胞术结果显示 RBNPs 可显著升高卵巢癌细胞凋亡率;Western blot 分析结果显示,RBNPs 可上调促凋亡蛋白 Cleaved Caspase-3、Bax 的表达,下调抗凋亡蛋白 Bcl-xl 表达,同时抑制 PI3K/AKT/mTOR 信号通路的活化,证实 RBNPs 能有效诱导卵巢癌细胞 SKOV3 和 CAOV3 凋亡.结论:RBNPS 可通过抑制 PI3K/AKT/mTOR 信号通路、调控凋亡相关蛋白表达,抑制卵巢癌细胞的增殖与迁移.
Objective:To explore the effects of self-assembled binary carrier-free nano-medicines(Rosmarinic acid/berberine carrier-free self-assembled nanoparticles,RBNPs)on the proliferation and migration of ovarian cancer cells SKOV3 and CAOV3 in vitro,as well as the underlying molecular mechanisms through regulating apoptosis-related proteins.Methods:We used two ovarian cancer cell lines,SKOV3 and CAOV3,to evaluate the effects of RBNPs on cell viability and long-term proliferation ability through CCK-8 assay,cloning experiments and scratch assays.The effects of RBNPs on cell migration ability were assessed through scratch as-says and Transwell experiments.The expressions of apoptosis-related proteins and proteins relat-ed to the PI3K/AKT/mTOR signaling pathway were analyzed by Western blot.Results:The CCK-8 assay demonstrated that RBNPs could reduce the activity of ovarian cancer cells.The cloning formation experiment indicated that RBNPs could significantly inhibit the proliferation ability of ovarian cancer cells.The scratch test and Transwell test jointly verified that RBNPs could significantly inhibit the migration ability of ovarian cancer cells,ruling out the interference of cell proliferation on the experimental results.The flow cytometry results showed that RBNPs could significantly increase the apoptosis rate of ovarian cancer cells.Western blot analysis re-sults indicated that RBNPs could up-regulate the expression of pro-apoptotic proteins Cleaved Caspase-3 and Bax,down-regulate the expression of anti-apoptotic protein Bcl-xl,and simulta-neously inhibit the activation of the PI3K/AKT/mTOR signaling pathway,confirming that RB-NPs can effectively induce the apoptosis of ovarian cancer cells SKOV3 and CAOV3.Conclu-sion:RBNPs can inhibit the proliferation and migration of ovarian cancer cells by suppressing the PI3K/AKT/mTOR signaling pathway and regulating the expression of apoptosis-related pro-teins.
刘云翼;薛彭元;郝明涛;王志伟;张雪阳;曲桂武;宋淑玲;曹奇志
山东医药大学,烟台 264003山东医药大学,烟台 264003山东医药大学,烟台 264003山东医药大学,烟台 264003山东医药大学,烟台 264003山东医药大学,烟台 264003山东医药大学,烟台 264003||山东省复杂医学智能与衰老重点实验室,烟台 264003山东医药大学,烟台 264003
医药卫生
RBNPs卵巢癌细胞凋亡增殖迁移
RBNPsOvarian cancerApoptosisProliferationMigration
《现代妇产科进展》 2026 (6)
415-420,6
山东省自然科学基金项目(No:ZR2024MH170)
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