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[EB病毒编码的潜伏膜蛋白1中涉及的c-Jun/Ets1之间的相互作用调节鼻咽癌中基质金属蛋白酶-9的表达]

[Cross-talk between c-Jun/Ets1 involved in EB virus-encoded latent membrane protein 1 regulates expression of matrix metalloproteinase-9 in nasopharyngeal carcinoma].

作者信息

Zeng Liang, Liu Yi-ping, Tao Yong-guang, Ai Mi-dan, Zhao Xiao-rong, Cao Ya

机构信息

Cancer Research Institute, Xiangya School of Medicine, Central South University, Changsha 410078, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2005 Apr;27(4):204-8.

Abstract

OBJECTIVE

To investigate effect of AP-1 and Ets binding site adjacent to matrix metalloproteinase-9 (MMP-9) promoter on activation of MMP-9 transcription of nasopharyngeal carcinoma cells transfected with EBV-encoded latent membrane protein 1 (LMP1), and to ascertain if cross-talk between c-Jun and Ets1 is involved in LMP1-regulating expression of MMP-9.

METHODS

Site-directed mutagenesis technique was used to establish a series of mutants, including MMP-9-CAT-Ets(-540)mt, MMP-9-CAT-AP-1(-533)mt and MMP-9-CAT-AP-1(-533)/Ets(-540)mt. After the mutants were transfected into LMP1-expressing NPC HNE2 cells regulated by Tet-on system (pTet-on-LMP1 HNE2), CAT activity of these mutants were assayed with induction of LMP1. With blockade of c-Jun or Ets1 antisense oligonucleotides, the activity of MMP-9 induced by LMP1 was assayed with gelatin zymography.

RESULTS

The CAT activity of MMP-9-Ets(-540)mt-CAT, MMP-9-AP-1(-533)mt-CAT, MMP-9-AP-1(-533)/Ets(-540) mt-CAT decreased significantly compared to MMP-9-CAT wt. After blockade with c-Jun or Ets1 antisense oligonucleotides, activity of MMP-9 induced by LMP1 decreased significantly, especially with combined blockade of c-Jun and Ets1.

CONCLUSION

The results suggest that transcription factor AP-1 and Ets play an crucial role in activation of MMP-9 transcription induced by LMP1, and cross-talk between c-Jun/Ets1 is involved in expression of MMP-9 mediated by LMP1.

摘要

目的

研究基质金属蛋白酶-9(MMP-9)启动子附近的活化蛋白-1(AP-1)和Ets结合位点对转染了EB病毒编码的潜伏膜蛋白1(LMP1)的鼻咽癌细胞中MMP-9转录激活的影响,并确定c-Jun和Ets1之间的相互作用是否参与LMP1调节的MMP-9表达。

方法

采用定点突变技术构建一系列突变体,包括MMP-9-CAT-Ets(-540)mt、MMP-9-CAT-AP-1(-533)mt和MMP-9-CAT-AP-1(-533)/Ets(-540)mt。将这些突变体转染到由Tet-on系统调控的表达LMP1的NPC HNE2细胞(pTet-on-LMP1 HNE2)中,在LMP1诱导下检测这些突变体的氯霉素乙酰转移酶(CAT)活性。用c-Jun或Ets1反义寡核苷酸阻断后,通过明胶酶谱法检测LMP1诱导的MMP-9活性。

结果

与野生型MMP-9-CAT相比,MMP-9-Ets(-540)mt-CAT、MMP-9-AP-1(-533)mt-CAT、MMP-9-AP-1(-533)/Ets(-540)mt-CAT的CAT活性显著降低。用c-Jun或Ets1反义寡核苷酸阻断后,LMP1诱导的MMP-9活性显著降低,尤其是c-Jun和Ets1联合阻断时。

结论

结果表明转录因子AP-1和Ets在LMP1诱导的MMP-9转录激活中起关键作用,c-Jun/Ets1之间的相互作用参与LMP1介导的MMP-9表达。

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