MiRNA-218, a new regulator of HMGB1, suppresses cell migration and invasion in non-small cell lung cancer

被引:72
|
作者
Zhang, Cailian [1 ]
Ge, Shengli [2 ]
Hu, Cailian [3 ]
Yang, Ning [1 ]
Zhang, Jinran [1 ]
机构
[1] Yanan Univ, Affiliated Hosp, Dept Geriatr, Yanan 716000, Peoples R China
[2] Yanan Univ, Affiliated Hosp, Dept Ophthalmol, Yanan 716000, Peoples R China
[3] Yanan Univ, Affiliated Hosp, Dept Pulm Med, Yanan 716000, Peoples R China
关键词
microRNA; miR-218; non-small lung cancer; HMGB1; TUMOR-SUPPRESSOR; HEPATOCELLULAR-CARCINOMA; ADP-RIBOSYLATION; BREAST-CANCER; INTACT-CELLS; EXPRESSION; MICRORNA; GENES; PROTEIN; INVASIVENESS;
D O I
10.1093/abbs/gmt109
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) function as negative regulators of gene expression involved in cancer metastasis. The aim of this study is to investigate the potential roles of miR-218 in non-small cell lung cancer and validate its regulation mechanism. Functional studies showed that miR-218 overexpression inhibited cell migration and invasion, but had no effect on cell viability. Enhanced green fluorescent protein reporter assay, real-time polymerase chain reaction and western blot analysis confirmed that miR-218 suppressed the expression of high mobility group box-1 (HMGB1) by directly targeting its 3'-untranslated region. Accordingly, silencing of HMGB1 accorded with the effects of miR-218 on cell migration and invasion, and overexpression of HMGB1 can restore cell migration and invasion which were reduced by miR-218. In conclusion, these findings demonstrate that miR-218 functions as a tumor suppressor in lung cancer. Furthermore, miR-218 may act as a potential therapeutic biomarker for metastatic lung cancer patients.
引用
收藏
页码:1055 / 1061
页数:7
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