机构地区:[1]南京中医药大学中医学院中西医结合学院,江苏省南京市210023
出 处:《中医杂志》2021年第16期1427-1433,共7页Journal of Traditional Chinese Medicine
基 金:国家自然科学基金(81873021);江苏省中医药科技发展专项(2020ZX01)。
摘 要:目的探讨黄芪-莪术-重楼配伍抗结肠癌转移的可能作用机制。方法38只裸鼠采用随机数字表法分为空白组8只及模型组、5-氟尿嘧啶(5-Fu)组和黄芪-莪术-重楼组各10只。除空白组外,其余各组裸鼠采用人结肠癌HCT116细胞原位移植法构建结肠癌原位移植瘤模型。造模24h后,5-Fu组给予注射用5-Fu 25mg/(kg·d)腹腔注射,隔日1次;黄芪-莪术-重楼组给予5.85g/(kg·d)黄芪-莪术-重楼药液灌胃,每日1次;空白组、模型组分别以10ml/(kg·d)生理盐水灌胃,每日1次。连续给药21天后计算瘤重及抑瘤率;检测各组裸鼠肿瘤及癌旁组织中酪氨酸激酶底物5(Tks5)、皮层肌动蛋白(Cortactin)、磷酸化皮层肌动蛋白(p-Cortactin)、细胞分裂周期蛋白(Cdc42)、衔接蛋白1(Nck1)、丝状肌动蛋白(F-actin)及膜型基质金属蛋白酶1(MT1-MMP)蛋白表达。结果5-Fu组、黄芪-莪术-重楼组的抑瘤率分别为58.32%、45.77%。与模型组比较,黄芪-莪术-重楼组、5-Fu组平均瘤重均降低(P<0.01);5-Fu组与黄芪-莪术-重楼组平均瘤重比较差异无统计学意义(P>0.05)。与空白组比较,模型组、黄芪-莪术-重楼组及5-Fu组肿瘤组织及癌旁组织中侵袭性伪足前体核心蛋白Tks5、p-Cortactin,侵袭性伪足成熟相关蛋白Cdc42、Nck1、F-actin、MT1-MMP蛋白表达均升高(P<0.05或P<0.01)。与模型组比较,黄芪-莪术-重楼组及5-Fu组肿瘤组织及癌旁组织中侵袭性伪足前体核心蛋白Tks5、p-Cortactin,侵袭性伪足成熟相关蛋白Cdc42、Nck1、F-actin、MT1-MMP蛋白表达均降低(P<0.01)。结论黄芪-莪术-重楼配伍可通过抑制肿瘤侵袭性伪足的形成及成熟,从而抑制结肠癌的生长与转移。Objective To explore the possible mechanism of Huangqi-Ezhu-Chonglou(黄芪-莪术-重楼,Qi-Zhu-Lou)combination on metastatic colon cancer.Methods Thirty-eight nude mice were divided into blank group(n=8),model group(n=10),5-fluorouracil(5-Fu)group(n=10)and Qi-Zhu-Lou group(n=10)by using a random number table.The nude mice in all groups but the blank group were transplanted with human colon cancer HCT116 cells following the orthotopic transplantation method to develop the colon cancer-derived orthotopic transplant model.Twenty-four hours after modeling,the 5-Fu group was given intraperitoneal injection of 25 mg/(kg·d)5-Fu,once every other day;the Qi-Zhu-Lou group was administered with Qi-Zhu-Lou liquid of 5.85 g/(kg·d)by gavage,once daily;both the blank group and the model group were given 10 ml/(kg·d)normal saline by gavage,once daily.After 21 days of continuous administration,all nude mice were killed to calculate tumor weight and tumor inhibition rate;the expression of tyrosine kinase substrate 5(Tks5),cortical actin(Cortactin),phosphorylated cortical actin(p-Cortactin),cell division cyclin(Cdc42),adaptor protein 1(Nck1),filamentous actin(F-actin)and membrane-type matrix metalloproteinase 1(MT1-MMP)protein in tumors and paracancerous tissues of nude mice was detected in each group.Results The tumor inhibition rate of the 5-Fu group and the Qi-Zhu-Lou group was 58.32% and 45.77%,respectively,significantly lower than that of the model group(P<0.01),and with no significant difference between the two groups(P>0.05).The protein expressions of invadopodia core protein precursor Tks5 and p-Cortactin,as well as invadopodia maturation-associated protein Cdc42,Nck1,F-actin and MT1-MMP in the tumor and paracancerous tissues of the mice in the model group,Qi-Zhu-Lou group and 5-FU group were significantly higher than those in the blank group(P<0.05 or P<0.01),while lower than those in the model group(P<0.01).Conclusion Qi-Zhu-Lou combination may inhibit the growth and metastasis of colon cancer cells by inhibiting the
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