Leukemia inhibitory factor promotes EMT through STAT3-dependent miR-21 induction

被引:61
作者
Yue, Xuetian [1 ]
Zhao, Yuhan [1 ]
Zhang, Cen [1 ]
Li, Jun [1 ]
Liu, Zhen [1 ]
Liu, Juan [1 ]
Hu, Wenwei [1 ,2 ]
机构
[1] Rutgers State Univ, Rutgers Canc Inst New Jersey, Dept Radiat Oncol, New Brunswick, NJ 08903 USA
[2] Rutgers State Univ, Dept Pharmacol, New Brunswick, NJ 08903 USA
基金
美国国家卫生研究院;
关键词
LIF; miR-21; epithelial-mesenchymal transition; STAT3; EPITHELIAL-MESENCHYMAL TRANSITION; BREAST-CANCER CELLS; STEM-CELLS; COLORECTAL-CANCER; MICRORNA MIR-21; CARCINOMA CELLS; EXPRESSION; METASTASIS; TARGETS; INVASION;
D O I
10.18632/oncotarget.6756
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Leukemia inhibitory factor (LIF) is a multi-function cytokine. Its role in cancer is not well-understood. Recent studies including ours show that LIF is frequently overexpressed in many types of human tumors and promotes the progression and metastasis of tumors. However, the underlying mechanism of LIF's promoting effects on tumor progression and metastasis is poorly defined. Epithelial-mesenchymal transition (EMT) plays an important role in tumor metastasis. This study reports that LIF promotes EMT in human tumor cells. Overexpression of LIF promotes tumor cells to acquire mesenchymal features, including morphological changes of cells from epithelial-like to mesenchymal-like, increased expression levels of mesenchymal markers and decreased expression of epithelial markers. Knockdown of endogenous LIF reverses EMT in cancer cells. We further identified that LIF induces the expression of microRNA-21 (miR-21), which in turn mediates the promoting effect of LIF on EMT. LIF induces miR-21 expression through the activation of STAT3. Importantly, blocking miR-21 function greatly abolished the promoting effect of LIF on EMT and the migration ability of cancer cells. Taken together, results from this study identified an important function and a novel underlying mechanism of LIF in EMT and tumor metastasis.
引用
收藏
页码:3777 / 3790
页数:14
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