首页|期刊导航|中药新药与临床药理|益气解毒方下调PTGES2抑制鼻咽癌细胞迁移与侵袭的机制

益气解毒方下调PTGES2抑制鼻咽癌细胞迁移与侵袭的机制OA

Study on the Mechanism of Yiqi Jiedu Prescription Inhibiting Migration and Invasion of Nasopharyngeal Carcinoma Cells by Downregulating PTGES2

中文摘要英文摘要

目的 研究益气解毒方和前列腺素 E 合酶 2(Prostaglandin E synthase 2,PTGES2)对鼻咽癌 5-8F 细胞迁移与侵袭能力的影响以及两者间的关系.方法 (1)使用益气解毒方干预 5-8F 细胞,将细胞分为对照组、益气解毒方低浓度组(0.5 mg·mL-1)、益气解毒方高浓度组(1.0 mg·mL-1)和顺铂组(2 µg·mL-1).采用细胞划痕实验、Transwell 侵袭小室法检测细胞的迁移与侵袭能力,Western Blot 法检测 PTGES2、Vimentin、N-cadherin、E-cadherin 表达水平.(2)使用 PTGES2 过表达(oe-PTGES2)、过表达空载体(oe-NC)、PTGES2 沉默(sh-PTGES2)、沉默空载体(sh-NC)慢病毒分别感染 5-8F 细胞,联合益气解毒方(1.0 mg·mL-1)干预细胞,设置过表达分组:oe-NC 组、oe-NC+益气解毒方组、oe-PTGES2 组、oe-PTGES2+益气解毒方组;以及沉默分组:sh-NC 组、sh-NC+益气解毒方组、sh-PTGES 组、sh-PTGES2+益气解毒方组.采用细胞划痕实验、Transwell侵袭小室法检测细胞的迁移与侵袭能力,Western Blot 法检测 PTGES2、Vimentin、磷酸化 Akt(p-Akt)、N-cadherin、E-cadherin 蛋白表达水平.结果 (1)与对照组比较,益气解毒方高浓度组和顺铂组的细胞相对迁移率与侵袭率明显下降(P<0.01),PTGES2、Vimentin、N-cadherin 蛋白的表达降低(P<0.05,P<0.01),E-cadherin 蛋白的表达升高(P<0.05,P<0.01).(2)PTGES2 过表达和沉默慢病毒感染细胞后,实验结果显示:与 oe-NC 组 比 较,oe-PTGES2 组细胞相对迁移率、侵袭率上升(P<0.01);PTGES2、Vimentin、p-Akt、N-cadherin 蛋白的表达升高(P<0.05,P<0.01),E-cadherin 蛋白的表达降低(P<0.05);与 sh-NC 组比较,sh-PTGES2 组细胞相对迁移率、侵袭率下降(P<0.01),PTGES2、Vimentin、p-Akt、N-cadherin 蛋白的表达降低(P<0.01),E-cadherin 蛋白的表达升高(P<0.01).过表达或沉默 PTGES2 后联合益气解毒方干预,结果显示:与 oe-NC+益气解毒方组比较,oe-PTGES2+益气解毒方组细胞相对迁移率、侵袭率上升(P<0.01),p-Akt、N-cadherin 蛋白的表达升高(P<0.05,P<0.01),E-cadherin 蛋白的表达降低(P<0.05).与 sh-NC+益气解毒方组比较,sh-PTGES2+益气解毒方组细胞相对迁移率、侵袭率下降(P<0.01),PTGES2、Vimentin、p-Akt、N-cadherin 蛋白的表达降低(P<0.01),E-cadherin 蛋白的表达升高(P<0.01).结论 PTGES2 能促进鼻咽癌细胞的迁移与侵袭;益气解毒方对鼻咽癌细胞迁移与侵袭的抑制作用可能与下调 PTGES2/Akt 通路有关.

Objective To investigate the effects of Yiqi Jiedu Prescription(YJP)and prostaglandin E synthase 2(PTGES2)on the migration and invasion of nasopharyngeal carcinoma(NPC)5-8F cells,as well as the role of PTGES2 in the effects of YJP.Methods(1)5-8F cells were divided into a control group,a low-concentration YJP group(0.5 mg·mL-1),a high-concentration YJP group(1.0 mg·mL-1),and a cisplatin group(2 µg·mL-1).Wound healing assay and Transwell invasion assay were used to assess cell migration and invasion abilities.The protein expression levels of PTGES2,Vimentin,N-cadherin,and E-cadherin were determined by Western Blot.(2)5-8F cells were transduced with lentiviral vectors for PTGES2 overexpression(oe-PTGES2)and the corresponding negative control(oe-NC),or for PTGES2-targeting shRNA(sh-PTGES2)and its negative control(sh-NC).The transduced cells were treated with or without YJP(1.0 mg·mL-1).For the overexpression experiments,cells were divided into the oe-NC group,oe-NC+YJP group,oe-PTGES2 group,and oe-PTGES2+YJP group.For the knockdown experiments,cells were divided into the sh-NC group,sh-NC+YJP group,sh-PTGES2 group,and sh-PTGES2+YJP group.Wound healing assay and Transwell invasion assay were used to assess cell migration and invasion abilities,and Western Blot was performed to measure the protein expression levels of PTGES2,Vimentin,phosphorylated AKT(p-AKT),N-cadherin,and E-cadherin.Results(1)Compared with the control group,the high-concentration YJP group and the cisplatin group exhibited significantly lower relative migration and invasion rates(P<0.01),reduced protein expression of PTGES2,Vimentin,and N-cadherin,and increased expression of E-cadherin(P<0.05,P<0.01).(2)After lentiviral transduction,compared with the oe-NC group,the oe-PTGES2 group significantly enhanced relative migration and invasion rates(P<0.01),along with increased protein expression of PTGES2,Vimentin,p-AKT,and N-cadherin(P<0.05,P<0.01),and decreased E-cadherin expression(P<0.05).Compared with the sh-NC group,the sh-PTGES2 group exhibited reduced relative migration and invasion rates(P<0.01),downregulated protein expression of PTGES2,Vimentin,p-Akt,and N-cadherin(P<0.01),and upregulated E-cadherin expression(P<0.01).When combined with YJP treatment,compared with the oe-NC+YJP group,the relative migration and invasion rates of cells in the oe-PTGES2+YJP group were increased(P<0.01),the protein expression of p-Akt,and N-cadherin were elevated(P<0.05,P<0.01),and the expression of E-cadherin was decreased(P<0.05).In contrast,compared with the sh-NC+YJP group,the sh-PTGES2+YJP group showed reduced relative migration and invasion rates(P<0.01),decreased protein expression of PTGES2,Vimentin,p-Akt,and N-cadherin(P<0.01),and increased E-cadherin expression(P<0.01).Conclusion PTGES2 can promote the migration and invasion of NPC cells;the inhibitory effect of YJP on the migration and invasion of NPC cells may involve suppression of the PTGES2/AKT pathway.

刘思颖;张文青;刘洁;王贤文;何迎春

湖南中医药大学,湖南 长沙 410208||湖南中医药大学第一附属医院,湖南 长沙 410007湖南中医药大学,湖南 长沙 410208||湖南中医药大学第一附属医院,湖南 长沙 410007湖南中医药大学,湖南 长沙 410208||湖南省中医眼耳鼻喉科疾病防治与视功能保护工程技术研究中心,湖南 长沙 410208||湖南省中医药防治眼耳鼻喉科疾病重点实验室,湖南 长沙 410208湖南中医药大学,湖南 长沙 410208||湖南中医药大学第一附属医院,湖南 长沙 410007湖南中医药大学,湖南 长沙 410208||湖南省中医眼耳鼻喉科疾病防治与视功能保护工程技术研究中心,湖南 长沙 410208||湖南省中医药防治眼耳鼻喉科疾病重点实验室,湖南 长沙 410208

医药卫生

益气解毒方鼻咽癌前列腺素E合酶2(PTGES2)迁移侵袭5-8F细胞

Yiqi Jiedu Prescriptionnasopharyngeal carcinomaPTGES2migrationinvasion5-8F cells

《中药新药与临床药理》 2026 (9)

1675-1684,10

国家自然科学基金项目(82505683)湖南省自然科学基金项目(2023JJ30449,2023JJ30475)湖南省卫生健康委员会项目(20257618)湖南中医药大学研究生科研创新项目(2025CX032,CX20251197).

10.19378/j.issn.1003-9783.2026.09.007

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