陕西医学杂志
陝西醫學雜誌
협서의학잡지
Shaanxi Medical Journal
2015年
10期
1284-1285,1289
,共3页
吴晓玲%蔡东阁%刘变利%孙师元%李牧
吳曉玲%蔡東閣%劉變利%孫師元%李牧
오효령%채동각%류변리%손사원%리목
子宫内膜肿瘤%氧化苦参碱%肿瘤转移%基因表达调控 ,肿瘤
子宮內膜腫瘤%氧化苦參堿%腫瘤轉移%基因錶達調控 ,腫瘤
자궁내막종류%양화고삼감%종류전이%기인표체조공 ,종류
Endometrial neoplasms%Oxymatrine%Neoplasm metastasis%Gene expression regulation,ne-oplastic
目的:探讨氧化苦参碱对人子宫内膜癌细胞HEC‐1‐B增殖、侵袭转移的作用及其机制。方法:MTT法检测细胞增殖抑制率;Transw ell 小室法观察细胞侵袭转移的改变;Western blot及Real‐time PCR法检测p38、p‐p38、MMP‐2和MMP‐9表达水平的变化。结果:一定浓度氧化苦参碱可显著抑制子宫内膜癌细胞HEC‐1‐B的增殖、侵袭转移,并呈时间和剂量依赖性。氧化苦参碱可显著降低H EC‐1‐B细胞中p38及MMPs的表达水平。联合应用SB203580能够有效增强氧化苦参碱的抗肿瘤细胞侵袭转移能力。结论:氧化苦参碱可以抑制子宫内膜癌细胞的增殖、侵袭转移,并下调p38磷酸化以及MMP2、MMP9的表达。
目的:探討氧化苦參堿對人子宮內膜癌細胞HEC‐1‐B增殖、侵襲轉移的作用及其機製。方法:MTT法檢測細胞增殖抑製率;Transw ell 小室法觀察細胞侵襲轉移的改變;Western blot及Real‐time PCR法檢測p38、p‐p38、MMP‐2和MMP‐9錶達水平的變化。結果:一定濃度氧化苦參堿可顯著抑製子宮內膜癌細胞HEC‐1‐B的增殖、侵襲轉移,併呈時間和劑量依賴性。氧化苦參堿可顯著降低H EC‐1‐B細胞中p38及MMPs的錶達水平。聯閤應用SB203580能夠有效增彊氧化苦參堿的抗腫瘤細胞侵襲轉移能力。結論:氧化苦參堿可以抑製子宮內膜癌細胞的增殖、侵襲轉移,併下調p38燐痠化以及MMP2、MMP9的錶達。
목적:탐토양화고삼감대인자궁내막암세포HEC‐1‐B증식、침습전이적작용급기궤제。방법:MTT법검측세포증식억제솔;Transw ell 소실법관찰세포침습전이적개변;Western blot급Real‐time PCR법검측p38、p‐p38、MMP‐2화MMP‐9표체수평적변화。결과:일정농도양화고삼감가현저억제자궁내막암세포HEC‐1‐B적증식、침습전이,병정시간화제량의뢰성。양화고삼감가현저강저H EC‐1‐B세포중p38급MMPs적표체수평。연합응용SB203580능구유효증강양화고삼감적항종류세포침습전이능력。결론:양화고삼감가이억제자궁내막암세포적증식、침습전이,병하조p38린산화이급MMP2、MMP9적표체。
Objective:To investigate the effects and mechanisms of oxymatrine on invasion and metastasis of Endometrial carcinoma HEC‐1‐B cells .Methods :HEC‐1‐B cells were cultured in vitro and treated by 0 ,0 .5 ,1 .0 and 1 .5 mg/ml oxymatrine .Then cell growth curves assay and cell invasion assay using Transwell chamber was used to evaluate the effects of oxymatrine on invasion of HEC‐1‐B cells .The expression of p38 ,p‐p38 ,matrix metal‐loproteinases‐2(MMP‐2) and MMP‐9 were analysed by Western blot and Real‐time PCR .Results :Compared with control group ,oxymatrine (0 .5 ,1 .0 and 1 .5 mg/ml) treated groups significantly inhibited the proliferation and inva‐sive ability of HEC‐1‐B cells in a concentration‐and time‐dependent manner .In addition ,oxymatrine reduced the phosphorylation level of p38 protein and the mRNA levels of MMP‐2 and MMP‐9 .Moreover ,a p38 inhibitor‐SB203580 and oxymatrine excert synergistic inhibition effects on the expression of MMP‐2 and MMP‐9 in HEC‐1‐B cells .Conclusion:These findings suggest that a potential mechanism by which oxymatrine has an anti‐metastatic effects on endometrial cancer cells via directly down‐regulating the p38 signaling pathway .