| Literature DB >> 27347154 |
Y E Zeng1, Xing-Hong Yao2, Zhi-Ping Yan1, Jing-Xia Liu1, Xiao-Heng Liu1.
Abstract
The developmental process of epithelial-mesenchymal transition (EMT) occurs when epithelial cells acquire invasive mesenchymal cell characteristics, and the activation of this process has been indicated to be involved in tumor progression. EMT could be induced by growth factors, cytokines and matrix metalloproteinases (MMPs). sphingosine-1-phosphate (S1P) is a biologically-active lipid that plays an important role in cancer metastasis. S1P also contributes to the activation of EMT. However, the mechanism underlying S1P-induced EMT is unclear. Increased evidence has demonstrated that the cell surface glycocalyx is closed associated with S1P and plays an important role in tumor progression, suggesting that S1P-induced EMT could be Snail-MMP signaling-dependent. Thus, we hypothesize that an S1P-glycocalyx-Snail-MMP signaling axis mediates S1P-induced EMT. This is an essential step towards improved understanding of the underlying mechanism involved in S1P-regulted EMT, and the development of novel diagnostic and anticancer therapeutic strategies.Entities:
Keywords: epithelial-mesenchymal transition; glycoclayx; matrix metalloproteinase; sphingosine-1-phosphate
Year: 2016 PMID: 27347154 PMCID: PMC4907053 DOI: 10.3892/ol.2016.4661
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967