吉首大学学报(自然科学版) ›› 2023, Vol. 44 ›› Issue (1): 77-83.DOI: 10.13438/j.cnki.jdzk.2023.01.011

• 医药 • 上一篇    下一篇

桂枝茯苓汤含药血清对子宫内膜癌细胞的影响

袁小波,唐静,阳帆   

  1. (1.湖南交通工程学院护理学院,湖南 衡阳 421000;2.湘潭市第一人民医院医学转化中心,湖南 湘潭 411101)
  • 出版日期:2023-01-25 发布日期:2023-04-10
  • 通讯作者: 唐静(1984—),女,四川开江人,湖南交通工程学院护理学院讲师,硕士,主要从事肿瘤基础研究.E-mail:JSDX6666@126.com.
  • 作者简介:袁小波(1982—),男,湖南桂阳人,湖南交通工程学院护理学院讲师,硕士,主要从事肿瘤基础研究

Effect of Guizhi Fuling Decoction-Containing Serum on Endometrial Cancer Cells

YUAN Xiaobo,TANG Jing,YANG Fan   

  1. (1.College of Nursing,Hunan Institute of Transportation Engineering,Hengyang 421000,Hunan China;2.Medical Conversion Center,The First People's Hospital of Xiangtan City,Xiangtan 411101,Hunan China)
  • Online:2023-01-25 Published:2023-04-10

摘要:为探究桂枝茯苓汤含药血清是否通过调控3-磷酸肌醇激酶(PI3K)、蛋白激酶B(AKT),参与调控子宫内膜癌细胞增殖、上皮-间质转化(EMT)与凋亡,将72只SD大鼠分为健康组、桂枝茯苓汤高剂量组、桂枝茯苓汤中剂量组、桂枝茯苓汤低剂量组和奥沙利铂组,对各组大鼠灌胃相应剂量药物,从大鼠的腹主动脉取血制备含药血清,培养子宫内膜癌HEC-B细胞,分为对照组、含药血清高剂量组、含药血清中剂量组、含药血清低剂量组、奥沙利铂血清组、含药血清高剂量+通路激活剂组,向各组细胞培养基中加入相应血清及试剂.采用四甲基偶氮唑蓝(MTT)法检测各组细胞增殖情况,流式细胞术检测各组细胞凋亡情况,Western Blot法检测EMT相关蛋白E-钙黏蛋白(E-cadherin)、细胞波形蛋白(Vimentin)、N-钙黏蛋白(N-cadherin)表达水平及PI3K/AKT通路相关蛋白磷酸化水平.结果表明:与对照组相比,含药血清高剂量组、含药血清中剂量组、含药血清低剂量组的细胞生存率、Vimentin和N-cadherin蛋白表达量、PI3K和AKT磷酸化程度均显著降低(P<0.05),细胞凋亡率、E-cadherin蛋白表达量显著升高(P<0.05),且呈剂量依赖性;与含药血清高剂量组相比,含药血清高剂量+通路激活剂组的细胞生存率、Vimentin和N-cadherin蛋白表达量、PI3K和AKT磷酸化程度均显著升高(P<0.05),细胞凋亡率、E-cadherin蛋白表达量显著降低(P<0.05),奥沙利铂血清组各项指标无显著差异(P>0.05).说明桂枝茯苓汤通过调控PI3K/AKT通路,抑制相关蛋白磷酸化,阻碍细胞生长,加剧细胞凋亡,缓解EMT,从而缓解子宫肌瘤病情.

关键词: 桂枝茯苓汤, 3-磷酸肌醇激酶, 蛋白激酶B, 子宫内膜癌, 细胞增殖, 细胞凋亡, 上皮-间质转化

Abstract: The purpose of this study was to investigate the effect of Guizhi Fuling Decoction-containing serum in regulation of endometrial cancer cell proliferation,epithelium-mesenchymal transformation (EMT) and apoptosis through the regulation of inositol 3-phosphate kinase (PI3K) and protein kinase B (AKT).Seventy-two SD rats were divided into healthy group,high-dose Guizhi Fuling Decoction group,middle-dose Guizhi Fuling Decoction group,low-dose Guizhi Fuling Decoction group and oxaliplatin group.Corresponding doses of drugs were given by gavage,and blood was drawn from the abdominal aorta to prepare drug-containing serum.Human endometrial cancer HEC-B cells were cultured and grouped into control group,high-dose drug-containing serum group,medium-dose drug-containing serum group,low-dose drug-containing serum group,oxaliplatin serum group,high-dose drug-containing serum + pathway activator group.Corresponding serum and reagents were added to the cell culture medium of each group.The proliferation of cells in each group was detected by tetramethylazolyl blue (MTT) method;cell apoptosis in each group was detected by flow cytometry;the expression levels of EMT-related proteins E-cadherin (E-cadherin),cellular vimentin (Vimentin),N-cadherin (N-cadherin) and the phosphorylation levels of PI3K/AKT pathway-related proteins were detected by Western Blot.Compared with the control group,the cell survival rate,Vimentin,N-cadherin protein expression,PI3K and AKT phosphorylation levels in the high-dose drug-containing serum group,the medium-dose drug-containing serum group,and the low-dose drug-containing serum group were obviously decreased (P<0.05);while the apoptosis rate and E-cadherin protein expression were obviously increased (P<0.05),in a dose-dependent manner.Compared with the high-dose drug-containing serum group,the cell survival rate,Vimentin,N-cadherin protein expression,PI3K and AKT phosphorylation levels in the high-dose drug-containing serum + pathway activator group were obviously increased (P<0.05),and the apoptosis rate and E-cadherin protein expression were obviously decreased (P<0.05),and there was no significant difference in each index between the oxaliplatin serum group (P>0.05).Guizhi Fuling Decoction regulates the PI3K/AKT pathway to inhibit the phosphorylation of related proteins,hinder cell growth,aggravate cell apoptosis,relieve EMT,and thus alleviate the condition of uterine fibroids.

Key words: Guizhi Fuling Decoction, phosphatidylinositide 3-kinase, protein kinase B, endometrial cancer, cell proliferation, cell apoptosis, epithelial-mesenchymal transition

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