ID | 113044 |
Author |
Obayashi, Mariko
Hiroshima University
Yoshida, Maki
Hiroshima University|Tokyo Medical University
Tsunematsu, Takaaki
The University of Tokushima
Tokushima University Educator and Researcher Directory
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Ogawa, Ikuko
Hiroshima University
Sasahira, Tomonori
Nara Medical University
Kuniyasu, Hiroki
Nara Medical University
Abiko, Yoshimitsu
Nihon University
Xu, Dan
Hiroshima University|Dalian Maritime University
Fukunaga, Saori
Hiroshima University
Tahara, Hidetoshi
Hiroshima University
Kudo, Yasusei
The University of Tokushima
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Nagao, Toshitaka
Tokyo Medical University
Takata, Takashi
Hiroshima University
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Keywords | invasion
microRNA (miRNA)
epithelial-mesenchymal transition (EMT)
head and neck squamous cell carcinoma (HNSCC)
microarray
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Content Type |
Journal Article
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Description | Head and neck squamous cell carcinoma (HNSCC) has a high capacity for invasion. To identify microRNAs (miRNAs) that regulate HNSCC invasion, we compared miRNA expression profiles between a parent HNSCC cell line and a highly invasive clone. The miR-200 family and miR-203 were downregulated in the clone. Here we focused on the role of miR-203 in invasion and epithelial-mesenchymal transition (EMT) induction in HNSCC. miR-203 was downregulated during EMT induction. Moreover, ectopic overexpression of miR-203 suppressed the invasion and induced mesenchymal-epithelial transition (MET) in HNSCC cells. Interestingly, we identified NUAK family SNF1-like kinase 1 (NUAK1) as a novel target gene of miR-203 by cyclopedic analysis using anti-Ago2 antibody. Increased expression of NUAK1 was observed during EMT induction, and ectopic expression of miR-203 delayed EMT induction by suppressing NUAK1 expression. Moreover, NUAK1 overexpression promoted the invasion of HNSCC cells. Importantly, NUAK1 expression was well correlated with poor differentiation, invasiveness, and lymph node metastasis in HNSCC cases. Overall, miR-203 has a tumor-suppressing role in invasion and EMT induction by targeting NUAK1 in HNSCC, suggesting miR-203 as a potential new diagnostic and therapeutic target for the treatment of HNSCC.
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Journal Title |
Oncotarget
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ISSN | 19492553
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Publisher | Impact Journals, LLC
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Volume | 7
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Issue | 7
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Start Page | 8223
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End Page | 8239
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Published Date | 2016-01-22
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Remark | This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0)(https://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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EDB ID | |
DOI (Published Version) | |
URL ( Publisher's Version ) | |
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language |
eng
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TextVersion |
Publisher
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departments |
Medical Sciences
Oral Sciences
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