标题:Regulation of metastasis of pediatric multiple myeloma by MMP13.
作者:Xiaoru Wang;Xiaocang Cao
作者机构:[Wang, X] Department of Pediatrics, Provincial Hospital affiliated to Shandong University, 324 Jingwu Road, Jinan, Shandong 250021, China;[ Cao, X] D 更多
通讯作者:Wang, XR
通讯作者地址:[Wang, XR]Shandong Univ, Dept Pediat, Prov Hosp, 324 Jingwu Rd, Jinan 250021, Shandong, Peoples R China.
来源:Tumour biology: the journal of the International Society for Oncodevelopmental Biology and Medicine
出版年:2014
卷:35
期:9
页码:8715-8720
DOI:10.1007/s13277-014-2147-y
关键词:Multiple myeloma; FGFR4; MMP13; ERK/MAPK; PI3K; JNK
摘要:The molecular mechanism underlying metastasis of pediatric multiple myeloma (MM) remains elusive. Here, we showed that the levels of MMP13 are significantly higher in MM from young patients than those from adult patients. Moreover, a strong correlation of the MMP13 and phosphorylated fibroblast growth factor receptor 4 (FGFR4) levels was detected in MM from young patients. To prove a causal link between activation of fibroblast growth factor receptors (FGFR) signaling pathway and MMP13 expression, we used a human MM line, RPMI-8226 (8226), to study the underlying molecular basis. We found that FGF1-induced FGFR4 phosphorylation in 8,226 cells resulted in significant activation of MMP13, and consequently, an increase in cancer invasiveness. FGFR4 inhibition in 8,226 cells abolished FGF1-stimulated MMP13 expression, suggesting that activation of FGFR signaling pathway in MM may promote cancer metastasis by inducing MMP13 expression. To define the signaling cascades downstream of FGFR4 activation for MMP13 activation, we applied specific inhibitors for PI3K, Jun N-terminal kinase (JNK), and ERK/MAPK, respectively, to the FGF1-stimulated 8,226 cells. We found that only inhibition of ERK1/2 significantly decreased the activation of MMP13 in response to FGF stimulation, suggesting that activation of FGFR signaling may activate ERK/MAPK, rather than JNK or PI3K pathway to activate MMP13 expression in 8,226 cells. Our study thus highlights FGFR4 signaling pathway and MMP13 as novel therapeutic targets for MM.
收录类别:SCOPUS;SCIE
WOS核心被引频次:9
Scopus被引频次:9
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84919843972&doi=10.1007%2fs13277-014-2147-y&partnerID=40&md5=f30dc78e32b600128d1ecf46665dbab5
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