| Literature DB >> 23479198 |
Min Deng1, Qiurong Ye, Zailong Qin, Ying Zheng, Wei He, Hailin Tang, Yanhong Zhou, Wei Xiong, Ming Zhou, Xiaoling Li, Qun Yan, Jian Ma, Guiyuan Li.
Abstract
LTF (lactotransferrin, or lactoferrin) plays important role in innate immunity, and its anti-tumor function has also been reported in multiple cancers. We previously reported that LTF is significantly down-regulated in nasopharyngeal carcinoma (NPC) and acts as a tumor suppressor by suppressing AKT signaling. However, the exact mechanism of the down-regulation of LTF in NPC has not been revealed. In the current study, we screened and identified LTF is a bona fide target of miR-214 in NPC cells. miR-214 mimics significantly suppressed LTF mRNA and protein expression levels in NPC cells. miR-214 not only can promote NPC cell proliferation and invasion abilities in vitro, but also can accelerate tumor formation and lung metastasis in a mouse xenograft model. The pro-tumor function of miR-214 was depended on LTF suppression since LTF re-expression can reverse it. miR-214 can also activate AKT signaling by suppressing LTF expression. Furthermore, miR-214 expression level was up-regulated in NPC especially in metastasis-prone NPC tumor tissues compared with normal nasopharyngeal epithelial tissues, while the LTF expression level was negatively correlated with miR-214, suggesting that miR-214 targeting is partly responsible for LTF down-regulation in NPC specimens.Entities:
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Year: 2013 PMID: 23479198 DOI: 10.1007/s13277-013-0718-y
Source DB: PubMed Journal: Tumour Biol ISSN: 1010-4283