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miR-106b对宫颈癌SiHa细胞运动侵袭功能的影响

Effects of miR-106b on migration and invasiveness of cervical cancer cells SiHa
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摘要 目的研究miR-106b对宫颈癌SiHa细胞转移侵袭功能的影响及作用机制。方法 SiHa细胞转染miR-106b inhibitors和mimics,实时定量PCR检测转染效率,Transwell及划痕法检测细胞运动侵袭功能,分析E-cad-herin、PTEN、p-AKT(Ser473)蛋白表达情况。结果 miR-106b inhibitors和mimics改变SiHa细胞中miR-106b表达。转染miR-106b inhibitors后,细胞迁移数、移动距离减少(P<0.05);PTEN及E-cadherin表达增强,p-AKT表达降低。转染miR-106b mimics后,细胞迁移数、移动距离增加(P<0.05);PTEN及E-cadherin表达降低,p-AKT表达增强。结论 miR-106b可能通过E-cadherin/AKT、PTEN/AKT信号通路影响SiHa细胞运动侵袭功能。 Objective To explore the effect of miR-106b on migration and invasiveness of cervical cancer cells SiHa and its possible mechanism.Methods miR-106b inhibitors and mimics were transiently transfected into SiHa cells,and the expression of miR-106b was detected by real-time PCR.Then,the function of migration and invasion of cells and the expression level of E-cadherin,PTEN and p-AKT were detected by Transwell,wound-healing and Western blotting assay.Results The expression of miR-106b was significantly altered by the miR-106b inhibitors and mimics in SiHa cells.Compared with negative control cells,knockdown of miR -106b expression dramatically decreased the number of cell invasion and the cell migration function (P<0.05).The expression of E-cadherin and PTEN were enhanced,but the p-AKT level was inhibited.On the contrary,compared with negative control cells,over expression of miR-106b significantly increased the cell invasion number and the cell migration function ( P<0.05).The expression of E-cadherin and PTEN were decreased,but the p-AKT level was enhanced.Conclusion The function of SiHa cells migration and invasion may be modulated by miR-106b through the signal pathway of E-cadherin/AKT and PTEN/AKT.
出处 《中国当代医药》 2013年第24期9-11,共3页 China Modern Medicine
基金 国家自然科学基金(81272859) 郑州大学第一附属医院青年创新基金
关键词 miR-106b 宫颈癌 转移 PTEN E-CADHERIN miR-106b Cervical cancer Metastasis PTEN E-cadherin
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  • 1Reddy P,Liu L,Ren C,et al.Formation of E-cadherin-mediated cell-cell adhesion activates AKT and mitogen activated protein kinase via phosphatidylinositol 3 kinase and ligand-independent activation of epidermal growth factor receptor in ovarian cancer cells[J].Mol Endocrinol,2005,19:2564-2578 被引量:1
  • 2Psyrri A,Kassar M,Yu Z,et al.Effect of epidermal growth factor receptor expression level on survival in patients with epithelial ovarian cancer[J].Clin Cancer Res,2005,11:8637-8643 被引量:1
  • 3Pece S,Gutkind JS.Signaling from E-cadherins to the MAPK pathway by the recruitment and activation of epidermal growth factor receptors upon cell-cell contact formation[J].J Biol Chem,2000,275:41227-41233 被引量:1
  • 4Fedor-Chaiken M,Hein PW,Stewart JC,et al.E-cadherin binding modulates EGF receptor activation[J].Cell Commun Adhes,2003,10:105-118 被引量:1
  • 5Shen X,Kramer RH.Adhesion-mediated squamous cell carcinoma survival through ligand-independent activation of epidermal growth factor receptor[J ].Am J Pathol,2004,165:1315-1329 被引量:1
  • 6Nicosia SV,Bai W,Cheng JQ,et al.Oncogenic pathways implicated in ovarian epithelial cancer[J].Hematol Oncol Clin North Am,2003,17:927-943 被引量:1
  • 7Fraser M,Leung B,Jahani-Asl A,et al.Chemoresistance in human ovarian cancer:the role of apoptotic regulators[J].Reprod Biol Endocrinol,2003,1:66-79 被引量:1
  • 8Arbyn M, Castelisague X, de Sanjose S, Bruni L, Saraiya M, Bray F, et al. Worldwide burden of cervical cancer in 2008. Ann Oncol 2011; 22: 2675-2686. 被引量:1
  • 9Kim VN, Han J, Siomi MC. Biogenesis of small RNAs in animals. Nat Rev Mol Cell Biol 2009; 10: 126-139. 被引量:1
  • 10Bartel DP. MicroRNAs: target recognition and regulatory functions. Cell 2009; 136: 215-233. 被引量:1

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