TY - JOUR
T1 - S100P/RAGE signaling regulates microRNA-155 expression via AP-1 activation in colon cancer
AU - Onyeagucha, Benjamin Chidi
AU - Mercado-Pimentel, Melania E.
AU - Hutchison, Jennifer
AU - Flemington, Erik K.
AU - Nelson, Mark A.
N1 - Funding Information:
Grant support: This work is supported in part by the Cancer Biology Training grant T32 CA09213 , SPORE Developmental Research Program (Pilot Grant) P50 CA 95060 , and the More Graduate Education at Mountain States Alliance (MGE@MSA) Alliance for Graduate Education and the Professoriate (AGEP) National Science Foundation (NSF) Cooperative Agreement No. HRD-0450137.
PY - 2013/8/1
Y1 - 2013/8/1
N2 - Accumulating evidence indicates that elevated S100P promotes the pathogenesis of cancers, including colon cancer. S100P exerts its effects by binding to and activating the Receptor for Advance Glycation End-products (RAGE). The effects of up-regulated S100P/RAGE signaling on cell functions are well documented. Despite these observations, little is known about the downstream targets of S100P/RAGE signaling. In the present study, we demonstrated for the first time that activation of RAGE by S100P regulates oncogenic microRNA-155 (miR-155) expression through Activator Protein-1 (AP-1) stimulation in colon cancer cells. Ectopic S100P up-regulated miR-155 levels in human colon cancer cells. Conversely, knockdown of S100P resulted in a decrease in miR-155 levels. Exogenous S100P induced miR-155 expression, but blockage of the RAGE with anti-RAGE antibody suppressed the induction of miR-155 by exogenous S100P. Attenuation of AP-1 activation through pharmacological inhibition of MEK activation or genetic inhibition of c-Jun activation using dominant negative c-Jun (TAM67) suppressed miR-155 induction by exogenous S100P. Also, S100P treatment stimulated the enrichment of c-Fos, an AP-1 family member, at the miR-155 host gene promoter site. Finally, a functional study demonstrated that miR-155 knockdown decreases colon cancer cell growth, motility, and invasion. Altogether, these data demonstrate that the expression of miR-155 is regulated by S100P and is dependent on RAGE activation and stimulation of AP-1.
AB - Accumulating evidence indicates that elevated S100P promotes the pathogenesis of cancers, including colon cancer. S100P exerts its effects by binding to and activating the Receptor for Advance Glycation End-products (RAGE). The effects of up-regulated S100P/RAGE signaling on cell functions are well documented. Despite these observations, little is known about the downstream targets of S100P/RAGE signaling. In the present study, we demonstrated for the first time that activation of RAGE by S100P regulates oncogenic microRNA-155 (miR-155) expression through Activator Protein-1 (AP-1) stimulation in colon cancer cells. Ectopic S100P up-regulated miR-155 levels in human colon cancer cells. Conversely, knockdown of S100P resulted in a decrease in miR-155 levels. Exogenous S100P induced miR-155 expression, but blockage of the RAGE with anti-RAGE antibody suppressed the induction of miR-155 by exogenous S100P. Attenuation of AP-1 activation through pharmacological inhibition of MEK activation or genetic inhibition of c-Jun activation using dominant negative c-Jun (TAM67) suppressed miR-155 induction by exogenous S100P. Also, S100P treatment stimulated the enrichment of c-Fos, an AP-1 family member, at the miR-155 host gene promoter site. Finally, a functional study demonstrated that miR-155 knockdown decreases colon cancer cell growth, motility, and invasion. Altogether, these data demonstrate that the expression of miR-155 is regulated by S100P and is dependent on RAGE activation and stimulation of AP-1.
KW - AP-1
KW - Colon cancer
KW - MiR-155
KW - MiR-155 sponge
KW - RAGE
KW - S100P
UR - https://www.scopus.com/pages/publications/84879880601
UR - https://www.scopus.com/inward/citedby.url?scp=84879880601&partnerID=8YFLogxK
U2 - 10.1016/j.yexcr.2013.05.009
DO - 10.1016/j.yexcr.2013.05.009
M3 - Article
C2 - 23693020
AN - SCOPUS:84879880601
SN - 0014-4827
VL - 319
SP - 2081
EP - 2090
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 13
ER -