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miR-375 Regulates Invasion-Related Proteins Vimentin and L-Plastin

Authors :
Jihyeon Lim
Ruth Hogue Angeletti
Thomas J. Belbin
Nicole Kawachi
Thomas J. Ow
Thomas M. Harris
Jeffrey E. Segall
Michael B. Prystowsky
Berta Burd
Geoffrey Childs
Lizandra Jimenez
Source :
The American journal of pathology. 187(7)
Publication Year :
2017

Abstract

Invasion is a hallmark of advanced head and neck squamous cell carcinoma (HNSCC). We previously determined that low relative miR-375 expression was associated with poor patient prognosis. HNSCC cells with increased miR-375 expression have lower invasive properties and impaired invadopodium activity. Using stable isotope labeling with amino acids in cell culture and reverse-phase liquid chromatography mass spectrometry, we assessed the impact of miR-375 expression on protein levels in UM-SCC-1 cells. Increased miR-375 expression was associated with down-regulation of proteins involved in cellular assembly and organization, death and survival, and movement. Two invasion-associated proteins, vimentin and L-plastin, were strongly down-regulated by miR-375. Luciferase reporter assays demonstrated that high miR-375 expression reduced vimentin promoter activity, suggesting that vimentin is an indirect target of miR-375. Runt-related transcription factor 1 (RUNX1) is a potential miR-375 direct target, and its knockdown reduced vimentin and L-plastin expression. Data in The Cancer Genome Atlas HNSCC database showed a significant inverse correlation between miR-375 expression and RUNX1, vimentin, and L-plastin RNA expression. These clinical correlations validate our in vitro model findings and support a mechanism in which miR-375 suppresses RUNX1 levels, resulting in reduced vimentin and L-plastin expression. Furthermore, knockdown of RUNX1, L-plastin, and vimentin resulted in significant reductions in cell invasion in vitro , indicating the functional significance of miR-375 regulation of specific proteins involved in HNSCC invasion.

Details

ISSN :
15252191
Volume :
187
Issue :
7
Database :
OpenAIRE
Journal :
The American journal of pathology
Accession number :
edsair.doi.dedup.....90db5f7db190b6eeacacd1012f09ee19