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microRNA-203 suppresses invasion and epithelial-mesenchymal transition induction via targeting NUAK1 in head and neck cancer

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 cl...

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Autores principales: Obayashi, Mariko, Yoshida, Maki, Tsunematsu, Takaaki, Ogawa, Ikuko, Sasahira, Tomonori, Kuniyasu, Hiroki, Imoto, Issei, Abiko, Yoshimitsu, Xu, Dan, Fukunaga, Saori, Tahara, Hidetoshi, Kudo, Yasusei, Nagao, Toshitaka, Takata, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884988/
https://www.ncbi.nlm.nih.gov/pubmed/26882562
http://dx.doi.org/10.18632/oncotarget.6972
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author Obayashi, Mariko
Yoshida, Maki
Tsunematsu, Takaaki
Ogawa, Ikuko
Sasahira, Tomonori
Kuniyasu, Hiroki
Imoto, Issei
Abiko, Yoshimitsu
Xu, Dan
Fukunaga, Saori
Tahara, Hidetoshi
Kudo, Yasusei
Nagao, Toshitaka
Takata, Takashi
author_facet Obayashi, Mariko
Yoshida, Maki
Tsunematsu, Takaaki
Ogawa, Ikuko
Sasahira, Tomonori
Kuniyasu, Hiroki
Imoto, Issei
Abiko, Yoshimitsu
Xu, Dan
Fukunaga, Saori
Tahara, Hidetoshi
Kudo, Yasusei
Nagao, Toshitaka
Takata, Takashi
author_sort Obayashi, Mariko
collection PubMed
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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spelling pubmed-48849882016-06-17 microRNA-203 suppresses invasion and epithelial-mesenchymal transition induction via targeting NUAK1 in head and neck cancer Obayashi, Mariko Yoshida, Maki Tsunematsu, Takaaki Ogawa, Ikuko Sasahira, Tomonori Kuniyasu, Hiroki Imoto, Issei Abiko, Yoshimitsu Xu, Dan Fukunaga, Saori Tahara, Hidetoshi Kudo, Yasusei Nagao, Toshitaka Takata, Takashi Oncotarget Research Paper 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. Impact Journals LLC 2016-01-22 /pmc/articles/PMC4884988/ /pubmed/26882562 http://dx.doi.org/10.18632/oncotarget.6972 Text en Copyright: © 2016 Obayashi et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Obayashi, Mariko
Yoshida, Maki
Tsunematsu, Takaaki
Ogawa, Ikuko
Sasahira, Tomonori
Kuniyasu, Hiroki
Imoto, Issei
Abiko, Yoshimitsu
Xu, Dan
Fukunaga, Saori
Tahara, Hidetoshi
Kudo, Yasusei
Nagao, Toshitaka
Takata, Takashi
microRNA-203 suppresses invasion and epithelial-mesenchymal transition induction via targeting NUAK1 in head and neck cancer
title microRNA-203 suppresses invasion and epithelial-mesenchymal transition induction via targeting NUAK1 in head and neck cancer
title_full microRNA-203 suppresses invasion and epithelial-mesenchymal transition induction via targeting NUAK1 in head and neck cancer
title_fullStr microRNA-203 suppresses invasion and epithelial-mesenchymal transition induction via targeting NUAK1 in head and neck cancer
title_full_unstemmed microRNA-203 suppresses invasion and epithelial-mesenchymal transition induction via targeting NUAK1 in head and neck cancer
title_short microRNA-203 suppresses invasion and epithelial-mesenchymal transition induction via targeting NUAK1 in head and neck cancer
title_sort microrna-203 suppresses invasion and epithelial-mesenchymal transition induction via targeting nuak1 in head and neck cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884988/
https://www.ncbi.nlm.nih.gov/pubmed/26882562
http://dx.doi.org/10.18632/oncotarget.6972
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