MiR-142 inhibits the development of cervical cancer by targeting HMGB1

被引:34
|
作者
Jiang, Daqiong [1 ]
Wang, Huiyan [2 ]
Li, Zhuyan [1 ]
Li, Zhen [1 ]
Chen, Xin [1 ]
Cai, Hongbing [1 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Hubei Key Lab Tumor Biol Behav, Dept Gynecol Oncol,Hubei Canc Clin Study Ctr, Wuhan 430071, Hubei, Peoples R China
[2] Hosp Wuhan Univ Technol, Dept Gynecol Oncol, Wuhan 430070, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-142; HMGB1; cervical cancer; BREAST-CANCER; PROGNOSTIC VALUE; MICRORNAS; EXPRESSION; PROLIFERATION;
D O I
10.18632/oncotarget.13136
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It has been reported that miRNAs is deregulated in diverse human cancers, involving human cervical cancer. However, the clinical significances and potential mechanisms of miR-142 in the development and progression of cervical cancer were not elucidated completely till now. In this study, we found that the expression of miR-142 was obviously down-regulated in human cervical cancer tissues and a panel of cell lines. According to statistics, the expression of miR-142 was negatively related to advanced FIGO stage and lymphatic metastasis (p < 0.001). Furthermore, our functional analysis revealed the overexpression of miR-142 affected cell proliferation and invasiveness, and enhanced cell apoptosis in representative SiHa and HeLa cells. Based on the molecular level, our findings showed the 3' untranslated region (3'-UTR) of high-mobility group box 1 protein (HMGB1) was a direct target of miR-142, and determined an inverse correlation with the expression of miR-142. Ectopic expression of HMGB1 could attenuate the inhibitory impact of miR-142 on the proliferation and invasiveness of cervical cancer cells. In conclusion, the present work suggested that miR-142 affects cervical cancer cell proliferation and invasiveness, and enhances cell apoptosis via directly targeting the expression of HMGB1, and these findings may lay a novel foundation for the promising therapy target of cervical cancer.
引用
收藏
页码:4001 / 4007
页数:7
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