| Literature DB >> 26190820 |
Ze-Peng Du1, Bing-Li Wu2, Yang-Min Xie3, Ying-Li Zhang2, Lian-Di Liao4, Fei Zhou3, Jian-Jun Xie2, Fa-Min Zeng2, Xiu-E Xu4, Wang-Kai Fang2, En-Min Li5, Li-Yan Xu6.
Abstract
Lipocalin 2 (LCN2) is a poor prognostic factor in esophageal squamous cell carcinoma (ESCC), however its functional roles and molecular mechanisms of action remain to be clarified. Here, we described the functions and signaling pathways for LCN2 in ESCC. Overexpression of LCN2 in ESCC cells accelerated cell migration and invasion in vitro, and promoted lung metastasis in vivo. Blocking LCN2 expression inhibited its pro-oncogenic effect. Either overexpression of LCN2 or treatment with recombinant human LCN2 protein enhanced the activation of MEK/ERK pathway, which in turn increases endogenous LCN2 to increase MMP-9 activity. The decreased p-cofilin and increased p-ERM induced by pERK1/2 cause the cytoskeleton F-actin rearrangement and alter the behavior of ESCC cells mediated by LCN2. As a consequence, activation of MMP-9 and the rearrangement of F-actin throw light on the mechanisms for LCN2 in ESCC. These results imply that LCN2 promotes the migration and invasion of ESCC cells through a novel positive feedback loop.Entities:
Keywords: Esophageal squamous cell carcinoma; Lipocalin 2; Migration and invasion of cancer cells; Positive feedback
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Year: 2015 PMID: 26190820 DOI: 10.1016/j.bbamcr.2015.07.007
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002