首页> 中文期刊> 《中华耳鼻咽喉头颈外科杂志》 >RNA干扰沉默HIF-1α对人鼻咽癌CNE-1细胞黏附和侵袭能力的影响

RNA干扰沉默HIF-1α对人鼻咽癌CNE-1细胞黏附和侵袭能力的影响

摘要

Objective To investagate the effects of HIF-1α on adhesion and invasion of human nasopharyngeal carcinoma CNE-1 cells under hypoxia and underlying molecular mechanisms.Methods CoCl2 was used to mimic tumor hypoxic microenvironment.mRNA and protein expressions of HIF-1α, E-cadherin and CXCR4 in CNE-1 cells at different hypoxic time phases were detected by RT-PCR and ELISA respectively.The influences of silencing HIF-1α using RNA interference on E-cadherin and CXCR4 expressions were evaluated.Adhesion test Transwell invasion test were used to evaluate the effects of HIF-1α gene silencing on cell adhesion and invasion.Results Under hypoxia, HIF-1α mRNA expression in CNE-1 cells was stable, but its protein expression increased obviously (P < 0.05).Both mRNA and protein expressions of E-cadherin were decreased significantly with prolonged hypoxia, while mRNA and protein expressions of CXCR4 increased significantly (P < 0.05).After silencing HIF-1αgene, expression of E-cadherin protein was up-regulated, but with down-regulated expression of CXCR4 protein, with a decrease significantly in adhesion rate or invasive cell number of CNE-1 cells (P < 0.05).Conclusions Hypoxia can increase HIF-1αprotein expression in nasopharyngeal carcinoma cell line CNE-1.Silencing HIF-1α by RNA interference can reduce inhesion and invasion abilities of CNE-1 cells, which may be mediated by down-regulating E-cadherin expression and up-regulating CXCR4 expression.%目的 探讨低氧诱导因子-1α(hypoxia inducible factor-1 alpha,HIF-1α)在低氧状态下,对人鼻咽癌CNE-1细胞黏附和侵袭能力的影响及其分子机制.方法 CoCl2模拟肿瘤低氧微环境.分别用RT-PCR和酶联免疫吸附法(ELISA)检测不同低氧时相HIF-1α、E-钙黏蛋白和趋化因子受体4(chemokine receptor 4,CXCR4)在mRNA及蛋白水平的表达情况.采用RNA干扰技术沉默HIF-1α检测其对E-钙黏蛋白、CXCR4蛋白表达的影响.分别采用黏附实验和Transwell侵袭实验检测HIF-1α沉默对CNE-1细胞黏附及侵袭能力的影响.结果 CNE-1细胞在低氧条件下,HIF-1 αmRNA表达相对恒定,而蛋白随低氧时间延长其表达明显升高(P <0.05);E-钙黏蛋白在mRNA及蛋白水平表达均显著降低,而CXCR4均显著升高(P<0.05).有效沉默HIF-1α可明显上调E-钙黏蛋白的蛋白表达,下调CXCR4表达.CNE-1细胞的黏附率和侵袭穿膜细胞数明显少(P<0.05).结论 低氧促进鼻咽癌CNE-1细胞中HIF-1α蛋白表达水平升高.有效沉默HIF-1α可降低CNE-1细胞的黏附和侵袭能力,其分子机制可能与上调E-钙黏蛋白、下调CXCR4表达有关.

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