| Literature DB >> 26193421 |
Melania E Mercado-Pimentel1, Benjamin C Onyeagucha2, Qing Li3, Angel C Pimentel4, Jana Jandova1, Mark A Nelson5.
Abstract
S100P signaling through the receptor for advanced glycation end-products (RAGE) contributes to colon cancer invasion and metastasis, but the mechanistic features of this process are obscure. Here, we investigate whether activation of S100P/RAGE signaling regulates oncogenic microRNA-21 (miR-21). We show that exogenous S100P up-regulates miR-21 levels in human colon cancer cells, whereas knockdown of S100P results in a decrease of miR-21. Furthermore, blockage of RAGE with anti-RAGE antibody suppresses S100P induction of miR-21. In addition, we found that S100P induction of miR-21 expression involves ERK and is suppressed by the MEK inhibitor U0126. Also, S100P treatment stimulates the enrichment of c-Fos, and AP-1 family members, at the miR-21 gene promoter.Entities:
Keywords: AP-1; Colon cancer; Inflammation; Metastasis; RAGE; RECK; TCGA; miR-21; microRNAs
Mesh:
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Year: 2015 PMID: 26193421 PMCID: PMC4582666 DOI: 10.1016/j.febslet.2015.07.010
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124