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首页|期刊导航|山东医药|Prohibitin1基因沉默对人黑色素瘤细胞铺展、迁移及侵袭的影响

Prohibitin1基因沉默对人黑色素瘤细胞铺展、迁移及侵袭的影响

毕佳佳

山东医药2016,Vol.56Issue(46):27-30,4.
山东医药2016,Vol.56Issue(46):27-30,4.DOI:10.3969/j.issn.1002-266X.2016.46.007

Prohibitin1基因沉默对人黑色素瘤细胞铺展、迁移及侵袭的影响

Effects of Prohibitin 1 gene silencing on spreading,migration and invasion of melanoma cells

毕佳佳1

作者信息

  • 1. 新乡医学院生命科学技术学院,河南新乡453003
  • 折叠

摘要

Abstract

Objective To investigate the effects of prohibitin 1 (PHB)silencing on spreading,migration and inva-sion of melanoma A375 cells by RNA interference (RNAi).Methods The A375 cells were divided into the control group and experimental group.The cells in the control group were cultured in DMEMcontaining 10%FBS,while the cells in the experimental group were treated with Lipofectamine2000 and PHB siRNA.After incubation for 24 hours,RT-PCR and Western blotting were used to detect the mRNA and protein expression of PHB in transfected A375 cells.Spreading experi-ment was performed for assessing the cell spreading at 30,60 and 120 min.The migration and invasion abilities of A375 cells were detected by Scratch and Transwell invasion assay,respectively.Results The mRNA and protein expression lev-els of PHB in the experimental group were lower than those in the control group (all P<0.01).Compared with the control group,the spreading cells in the experimental group were less at 30,60 and 120 min (all P<0.01).The migration area in the experimental group was significantly less than that in the control group at 12 and 24 h after wounding healing (P<0.01).Meanwhile,the invasive ability of the experimental group was less than that of the control group (P<0.01).Con-clusion PHB gene silencing can effectively inhibit the spreading,migration and invasion of melanoma cells.

关键词

抗增殖蛋白/黑色素瘤/细胞铺展/细胞迁移/侵袭/RN A干扰

Key words

prohibitin/melanoma/spreading/migration/invasion/RNA interference

分类

医药卫生

引用本文复制引用

毕佳佳..Prohibitin1基因沉默对人黑色素瘤细胞铺展、迁移及侵袭的影响[J].山东医药,2016,56(46):27-30,4.

基金项目

国家自然科学基金资助项目(81402416);新乡医学院博士科研启动经费资助项目(505057)。 ()

山东医药

OA北大核心CSTPCD

1002-266X

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