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白血病抑制因子通过STAT3依赖的miR-21诱导促进上皮-间质转化。

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

作者信息

Yue Xuetian, Zhao Yuhan, Zhang Cen, Li Jun, Liu Zhen, Liu Juan, Hu Wenwei

机构信息

Department of Radiation Oncology, Rutgers Cancer Institute of New Jersey, Rutgers State University of New Jersey, New Brunswick, NJ, USA.

Department of Pharmacology, Rutgers State University of New Jersey, New Brunswick, NJ, USA.

出版信息

Oncotarget. 2016 Jan 26;7(4):3777-90. doi: 10.18632/oncotarget.6756.

Abstract

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.

摘要

白血病抑制因子(LIF)是一种多功能细胞因子。其在癌症中的作用尚未得到充分了解。包括我们的研究在内的近期研究表明,LIF在多种人类肿瘤中经常过度表达,并促进肿瘤的进展和转移。然而,LIF促进肿瘤进展和转移的潜在机制尚不清楚。上皮-间质转化(EMT)在肿瘤转移中起重要作用。本研究报道LIF促进人类肿瘤细胞的EMT。LIF的过表达促进肿瘤细胞获得间质特征,包括细胞从上皮样形态转变为间质样形态、间质标志物表达水平增加以及上皮标志物表达减少。内源性LIF的敲低可逆转癌细胞中的EMT。我们进一步确定LIF诱导微小RNA-21(miR-21)的表达,进而介导LIF对EMT的促进作用。LIF通过激活STAT3诱导miR-21表达。重要的是,阻断miR-21功能极大地消除了LIF对EMT的促进作用以及癌细胞的迁移能力。综上所述,本研究结果确定了LIF在EMT和肿瘤转移中的重要功能及新的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a6/4826169/6f04179824c6/oncotarget-07-3777-g001.jpg

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