裂果薯皂苷Ⅰ体外抑制鼻咽癌细胞HONE-1作用及其机制OA
The effect and mechanism of Saponin Ⅰ of Schizocapsa plantaginea Hance on nasopharyngeal carcinoma cell line HONE-1 in vitro
目的 探讨裂果薯皂苷Ⅰ(SSPHⅠ)对人鼻咽癌HONE-1细胞的抑制作用及其相关分子机制.方法 采用CCK-8法检测SSPHⅠ对HONE-1细胞活性的影响;通过集落形成实验评估其对细胞增殖的抑制作用;利用Transwell实验分析细胞侵袭能力的变化;使用二氢吡啶(DHE)荧光探针检测细胞内活性氧(ROS)水平;通过乳酸脱氢酶(LDH)释放实验反映细胞内含物的释放程度;运用Annexin-V/PI双染法检测细胞焦亡率;并采用Western blot法检测经典焦亡通路相关蛋白的表达变化.结果 CCK-8结果显示,SSPHⅠ处理24 h后HONE-1细胞活性呈浓度依赖性降低,IC50值为3.383 μmol/L;集落形成实验中,随着SSPHⅠ浓度增加,HONE-1细胞集落形成数量逐渐减少(P<0.01);Transwell实验显示,SSPHⅠ处理后穿过小室的细胞数量减少(P<0.01);DHE荧光探针检测结果显示,SSPHⅠ处理后细胞内ROS荧光强度升高(P<0.001);LDH释放实验结果显示,细胞上清液中LDH活性随SSPHⅠ浓度增加而升高(P<0.001);Annexin-V/PI双染法检测结果显示,SSPHⅠ处理后Annexin-V/PI阳性细胞比例增加(P<0.001);Western blot结果显示,与对照组相比,SSPHⅠ处理组细胞中cleaved-Caspase-1和GSDMD-N-terminal蛋白表达水平上调(P<0.05),NLRP3蛋白表达水平亦升高(P<0.05);ELISA结果显示,细胞中IL-1β和IL-18含量均随SSPHⅠ浓度增加而升高(P<0.05).结论 SSPHⅠ可通过调控ROS/NLRP3/Caspase-1信号轴诱导鼻咽癌HONE-1细胞焦亡,从而发挥抗鼻咽癌作用,提示其可能作为治疗鼻咽癌的潜在药物.
Objective To explore the inhibitory effect and related molecular mechanisms of Saponin of Schizo-capsa plantaginea HanceⅠ(SSPHⅠ)on human nasopharyngeal carcinoma HONE-1 cells.Methods The effect of SSPHⅠ on HONE-1 cell viability was detected using the CCK-8 assay.Its inhibitory effect on cell proliferation was evaluated through a colony formation assay.Changes in cell invasion ability were analyzed using the Transwell assay.Intracellular reactive oxygen species(ROS)levels were measured using the DHE fluorescent probe.The ex-tent of intracellular content release was reflected by the LDH release assay.The rate of cell pyroptosis was detected using the Annexin-V/PI double staining method.Changes in the expression of proteins related to the classical py-roptosis pathway were examined by Western Blot.Results CCK-8 assay showed that treatment with SSPHⅠ for 24 hours reduced HONE-1 cell viability in a concentration-dependent manner,with an IC50 value of 3.383 μmol/L.In the colony formation assay,the number of HONE-1 cell colonies gradually decreased with increasing concentra-tions of SSPHⅠ(P<0.01).The Transwell assay revealed that the number of cells migrating through the chamber was reduced following SSPHⅠ treatment(P<0.01).DHE fluorescence probe detection indicated that intracellu-lar ROS fluorescence intensity increased after SSPHⅠ treatment(P<0.001).The LDH release assay showed that LDH activity in the cell supernatant increased with higher concentrations of SSPHⅠ(P<0.001).Annexin-V/PI double staining demonstrated that the proportion of Annexin-V/PI-positive cells increased after SSPHⅠ treatment(P<0.001).Western blot analysis showed that,compared with the control group,the protein expression levels of cleaved-Caspase-1 and GSDMD-N-terminal were upregulated in SSPH Ⅰ-treated cells(P<0.05),and NLRP3 protein expression levels also increased(P<0.05).ELISA results showed that the levels of IL-1β and IL-18 in the cells increased with higher concentrations of SSPHⅠ(P<0.05).Conclusion SSPHⅠ can induce pyroptosis in nasopharyngeal carcinoma HONE-1 cells by regulating the ROS/NLRP3/Caspase-1 signaling axis,thereby exert-ing an anti-nasopharyngeal carcinoma effect.This suggests that SSPHⅠ may serve as a potential therapeutic agent for nasopharyngeal carcinoma.
郭心怡;梁梓樱;王金妮;丁小莲;王燕雪;梁钢
广西医科大学 药学院,南宁 530021广西医科大学 药学院,南宁 530021广西医科大学 药学院,南宁 530021广西医科大学 药学院,南宁 530021广西医科大学 药学院,南宁 530021广西医科大学 药学院,南宁 530021||广西医科大学 靶向肿瘤学国家重点实验室,南宁 530021
医药卫生
SSPHⅠ鼻咽癌活性氧NLRP3焦亡皂苷
SSPHⅠnasopharyngeal carcinomareactive oxygen speciesNLRP3pyroptpsissaponin
《安徽医科大学学报》 2026 (4)
628-635,8
国家自然科学基金项目(编号:82360792)广西生物靶向诊治研究重点实验室开放课题项目(编 号:GXSWBX 202402) National Natural Science Foundation of China(No.82360792)Open Project of Guangxi Key Laboratory of Biological Targeting Diagnosis and Therapy Research(No.GXSWBX202402)
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