期刊文献+

干扰素调节因子-5在鼻咽癌组织中的表达及对鼻咽癌细胞侵袭和迁移的影响 被引量:2

Expression of Interferon Regulatory Factor-5 in Nasopharyngeal Carcinoma Tissue and Its Effect on Invasion and Migration of Nasopharyngeal Carcinoma Cells
原文传递
导出
摘要 [目的]检测鼻咽癌组织中干扰素调节因子-5(IRF-5)的表达,探讨其在鼻咽癌细胞CNE-1增殖、迁移与侵袭中的作用。[方法]采用定量聚合酶链反应(qPCR)测定鼻咽癌旁组织与鼻咽癌组织中IRF-5的表达水平。随机将CNE-1细胞分为正常对照组、空白病毒组和病毒转染组,分别采用MTT法测定各组细胞的增殖情况,采用划痕实验测定各组细胞的迁移能力,采用Transwell小室法测定各组细胞的侵袭能力,采用qPCR和Western blot法测定各组细胞IRF-5、金属蛋白酶-2(MMP-2)、E-cadherin、趋化因子-12(CXCL-12)和趋化因子受体-4(CXCR-4)mRNA和蛋白的表达水平。[结果](1)鼻咽癌组织中IRF-5 mRNA水平较癌旁组织显著降低(P<0.05);(2)病毒转染组细胞在培养24h、48h和72h时OD值均较正常对照组和空白病毒对照组显著降低(P<0.05);(3)病毒转染组细胞的划痕宽度较正常对照组和空白病毒对照组显著增大(P<0.05);(4)病毒转染组穿膜细胞数量较正常对照组和空白病毒对照组显著降低(P<0.05);(5)病毒转染组细胞的IRF-5和E-cadherin mRNA表达水平较正常对照组和空白病毒对照组显著升高,而MMP-2、CXCL-12和CXCR-4 mRNA表达水平较正常对照组和空白病毒对照组显著降低(P<0.05)。[结论] IRF-5的低表达可能与鼻咽癌的发生发展有关,过表达IRF-5能够抑制鼻咽癌细胞的增殖、迁移和侵袭,IRF-5可能通过增加E-cadherin表达而抑制MMP-2、CXCL-12和CXCR-4表达而发挥作用。 [Objective] To investigate the expression of interferon regulatory factor-5(IRF-5) in nasopharyngeal carcinoma(NPC) tissues,and its roles in the proliferation,migration and invasion of NPC cells.[Methods] The expression level of IRF-5 was measured by quantitative polymerase chain reaction(qRTPCR) in 65 specimens of NPC tissue and corresponding pericancerous mucosa. Human nasopharyngeal carcinoma CNE-1 cells were randomly divided into normal control group,blank virus group and virus transfection group,and the proliferation of cells were determined by MTT method,the migration ability of cells were determined by scratch test,the invasive ability of cells were determined by Transwell assay,and mRNA and protein expression levels of IRF-5,metalloproteinase-2(MMP-2),e-cadherin,chemokine-12(CXCL-12) and chemokine receptor-4(Cxcr-4) were determined by qRT-PCR and Western blot,respectively. [Results] The expression level of IRF-5 mRNA in NPC tissues was significantly lower than that in pericancerous tissues(P<0.05). OD values of cells in the virus transfection group were significantly lower than those in the normal control group and the blank virus group at 24 h,48 h and 72 h after culture(P<0.05). The scratch width of cells in the viral transfection group was significantly larger than that of the normal control group and the blank virus group(P<0.05). The number of membrane penetrating cells in the virus transfection group was significantly lower than that in the normal control group and the blank virus group(P<0.05). The expression levels of IRF-5 and E-cadherin mRNA in cells of the virus transfection group were significantly higher than those of the normal control group and the blank virus group,while expression levels of MMP-2,CXCL-12 and CXCR-4 mRNA were significantly lower than those of the normal control group and the blank virus group(P<0.05).[Conclusion] The low expression of IRF-5 may be related to the occurrence and development of NPC. Overexpression of IRF-5 could inhibit the proliferation,migration and invasion of NPC cells,and IRF-5 may inhibit the expression of MMP-2,CXCL-12 and CXCR-4 by increasing the expression of E-cadherin.
作者 高飞 贾霖 韩建军 王允 贾利 陈宓 何君 刘小军 代红春 GAO Fei;JIA Lin;HAN Jian-jun;WANG Yun;JIA Li;CHEN Mi;HE Jun;LIU Xiao-jun;DAI Hong-chun(The Third Hospital of Mianyang,Sichuan Mental Health Center,Mianyang 621000,China)
出处 《肿瘤学杂志》 CAS 2019年第12期1064-1069,共6页 Journal of Chinese Oncology
基金 四川省卫计委2018科研课题(18PJ210)
关键词 鼻咽肿瘤 干扰素调节因子-5 细胞迁移 细胞侵袭 ,nasopharyngeal carcinoma interferon regulatory factor-5 cell migration cell invasion
  • 相关文献

参考文献3

二级参考文献30

  • 1蒋玉萍,吴小华.趋化因子CXCL12及其受体与肿瘤转移的关系[J].癌症,2007,26(2):220-224. 被引量:21
  • 2罗君,吴小翎.趋化因子CXCL12及其受体CXCR4与肿瘤的关系[J].生命的化学,2007,27(2):177-179. 被引量:2
  • 3黄琛,武明花,李桂源.鼻咽癌转录组学研究的现状与进展[J].生物化学与生物物理进展,2007,34(11):1129-1135. 被引量:10
  • 4房宝英,何冬梅,张洹,陈丽.Bcl-2 shRNA诱导成人T淋巴细胞白血病细胞株Molt4凋亡的研究[J].暨南大学学报(自然科学与医学版),2007,28(6):541-545. 被引量:1
  • 5张文玲,周艳宏,肖岚,范松青,曾朝阳,李小玲,武明花,李桂源.鼻咽癌分子标志物研究[J].生物化学与生物物理进展,2008,35(1):7-13. 被引量:32
  • 6ARION D,UNGER T,LEWIS D A,et al.Molecular evidence for increased expression of genes related to immune and chaperone function in the prefrontal cortex in schizophrenia[J].Biol Psychiatry,2007,62(7):711-721.
  • 7HARRIS RA,NAGY-SZAKAL D,MIR SA,et al.DNA methylation-associated colonic mucosal immune and defense responses in treatment-naive pediatric ulcerative colitis[J].Epigenetics,2014,9(8):1131-1137.
  • 8ARION D,UNGER T,LEWIS D A,et al.Molecular evidence for increased expression of genes related to immune and chaperone function in the prefrontal cortex in schizophrenia[J].Biol Psychiatry,2007,62(7):711-721.
  • 9LEE J,GOH SH,SONG N,et al.Overexpression of IFITM1has clinicopathologic effects on gastric cancer and is regulated by an epigenetic mechanism[J].Am J Pathol,2012,181(1):43-52.
  • 10WILKINS C,WORODWARD J,LAU DT,et al.IFITM1is a tight junction protein that inhibits hepatitis C virus entry[J].Hepatology,2013,57(2):461-469.

共引文献8

同被引文献18

引证文献2

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部