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MicroRNA expression signature of oral squamous cell carcinoma: functional role of microRNA-26a/b in the modulation of novel cancer pathways

BACKGROUND: MicroRNAs (miRNAs) have been shown to play major roles in carcinogenesis in a variety of cancers. The aim of this study was to determine the miRNA expression signature of oral squamous cell carcinoma (OSCC) and to investigate the functional roles of miR-26a and miR-26b in OSCC cells. MET...

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Autores principales: Fukumoto, I, Hanazawa, T, Kinoshita, T, Kikkawa, N, Koshizuka, K, Goto, Y, Nishikawa, R, Chiyomaru, T, Enokida, H, Nakagawa, M, Okamoto, Y, Seki, N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453953/
https://www.ncbi.nlm.nih.gov/pubmed/25668004
http://dx.doi.org/10.1038/bjc.2015.19
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author Fukumoto, I
Hanazawa, T
Kinoshita, T
Kikkawa, N
Koshizuka, K
Goto, Y
Nishikawa, R
Chiyomaru, T
Enokida, H
Nakagawa, M
Okamoto, Y
Seki, N
author_facet Fukumoto, I
Hanazawa, T
Kinoshita, T
Kikkawa, N
Koshizuka, K
Goto, Y
Nishikawa, R
Chiyomaru, T
Enokida, H
Nakagawa, M
Okamoto, Y
Seki, N
author_sort Fukumoto, I
collection PubMed
description BACKGROUND: MicroRNAs (miRNAs) have been shown to play major roles in carcinogenesis in a variety of cancers. The aim of this study was to determine the miRNA expression signature of oral squamous cell carcinoma (OSCC) and to investigate the functional roles of miR-26a and miR-26b in OSCC cells. METHODS: An OSCC miRNA signature was constructed by PCR-based array methods. Functional studies of differentially expressed miRNAs were performed to investigate cell proliferation, migration, and invasion in OSCC cells. In silico database and genome-wide gene expression analyses were performed to identify molecular targets and pathways mediated by miR-26a/b. RESULTS: miR-26a and miR-26b were significantly downregulated in OSCC. Restoration of both miR-26a and miR-26b in cancer cell lines revealed that these miRNAs significantly inhibited cancer cell migration and invasion. Our data demonstrated that the novel transmembrane TMEM184B gene was a direct target of miR-26a/b regulation. Silencing of TMEM184B inhibited cancer cell migration and invasion, and regulated the actin cytoskeleton-pathway related genes. CONCLUSIONS: Loss of tumour-suppressive miR-26a/b enhanced cancer cell migration and invasion in OSCC through direct regulation of TMEM184B. Our data describing pathways regulated by tumour-suppressive miR-26a/b provide new insights into the potential mechanisms of OSCC oncogenesis and metastasis.
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spelling pubmed-44539532016-03-03 MicroRNA expression signature of oral squamous cell carcinoma: functional role of microRNA-26a/b in the modulation of novel cancer pathways Fukumoto, I Hanazawa, T Kinoshita, T Kikkawa, N Koshizuka, K Goto, Y Nishikawa, R Chiyomaru, T Enokida, H Nakagawa, M Okamoto, Y Seki, N Br J Cancer Molecular Diagnostics BACKGROUND: MicroRNAs (miRNAs) have been shown to play major roles in carcinogenesis in a variety of cancers. The aim of this study was to determine the miRNA expression signature of oral squamous cell carcinoma (OSCC) and to investigate the functional roles of miR-26a and miR-26b in OSCC cells. METHODS: An OSCC miRNA signature was constructed by PCR-based array methods. Functional studies of differentially expressed miRNAs were performed to investigate cell proliferation, migration, and invasion in OSCC cells. In silico database and genome-wide gene expression analyses were performed to identify molecular targets and pathways mediated by miR-26a/b. RESULTS: miR-26a and miR-26b were significantly downregulated in OSCC. Restoration of both miR-26a and miR-26b in cancer cell lines revealed that these miRNAs significantly inhibited cancer cell migration and invasion. Our data demonstrated that the novel transmembrane TMEM184B gene was a direct target of miR-26a/b regulation. Silencing of TMEM184B inhibited cancer cell migration and invasion, and regulated the actin cytoskeleton-pathway related genes. CONCLUSIONS: Loss of tumour-suppressive miR-26a/b enhanced cancer cell migration and invasion in OSCC through direct regulation of TMEM184B. Our data describing pathways regulated by tumour-suppressive miR-26a/b provide new insights into the potential mechanisms of OSCC oncogenesis and metastasis. Nature Publishing Group 2015-03-03 2015-02-10 /pmc/articles/PMC4453953/ /pubmed/25668004 http://dx.doi.org/10.1038/bjc.2015.19 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Molecular Diagnostics
Fukumoto, I
Hanazawa, T
Kinoshita, T
Kikkawa, N
Koshizuka, K
Goto, Y
Nishikawa, R
Chiyomaru, T
Enokida, H
Nakagawa, M
Okamoto, Y
Seki, N
MicroRNA expression signature of oral squamous cell carcinoma: functional role of microRNA-26a/b in the modulation of novel cancer pathways
title MicroRNA expression signature of oral squamous cell carcinoma: functional role of microRNA-26a/b in the modulation of novel cancer pathways
title_full MicroRNA expression signature of oral squamous cell carcinoma: functional role of microRNA-26a/b in the modulation of novel cancer pathways
title_fullStr MicroRNA expression signature of oral squamous cell carcinoma: functional role of microRNA-26a/b in the modulation of novel cancer pathways
title_full_unstemmed MicroRNA expression signature of oral squamous cell carcinoma: functional role of microRNA-26a/b in the modulation of novel cancer pathways
title_short MicroRNA expression signature of oral squamous cell carcinoma: functional role of microRNA-26a/b in the modulation of novel cancer pathways
title_sort microrna expression signature of oral squamous cell carcinoma: functional role of microrna-26a/b in the modulation of novel cancer pathways
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453953/
https://www.ncbi.nlm.nih.gov/pubmed/25668004
http://dx.doi.org/10.1038/bjc.2015.19
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