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

被引:68
|
作者
Obayashi, Mariko [1 ]
Yoshida, Maki [1 ,9 ]
Tsunematsu, Takaaki [2 ]
Ogawa, Ikuko [3 ]
Sasahira, Tomonori [4 ]
Kuniyasu, Hiroki [4 ]
Imoto, Issei [5 ]
Abiko, Yoshimitsu [6 ]
Xu, Dan [7 ,8 ]
Fukunaga, Saori [7 ]
Tahara, Hidetoshi [7 ]
Kudo, Yasusei [2 ]
Nagao, Toshitaka [9 ]
Takata, Takashi [1 ]
机构
[1] Hiroshima Univ, Inst Biomed & Hlth Sci, Dept Oral & Maxillofacial Pathobiol, Hiroshima, Japan
[2] Univ Tokushima, Grad Sch, Inst Hlth Biosci, Dept Oral Mol Pathol, Tokushima 770, Japan
[3] Hiroshima Univ Hosp, Ctr Oral Clin Examinat, Hiroshima, Japan
[4] Nara Med Univ, Sch Med, Dept Mol Pathol, Nara, Japan
[5] Univ Tokushima, Grad Sch, Inst Hlth Biosci, Dept Human Genet, Tokushima 770, Japan
[6] Nihon Univ, Sch Dent Matsudo, Dept Biochem, Chiba, Japan
[7] Hiroshima Univ, Grad Sch Biomed Sci, Dept Cellular & Mol Biol, Hiroshima, Japan
[8] Dalian Maritime Univ, Inst Environm Syst Biol, Dalian, Peoples R China
[9] Tokyo Med Univ, Dept Anat Pathol, Tokyo 1608402, Japan
基金
日本学术振兴会;
关键词
invasion; microRNA (miRNA); epithelial-mesenchymal transition (EMT); head and neck squamous cell carcinoma (HNSCC); microarray; SQUAMOUS-CELL CARCINOMA; LYMPH-NODE METASTASIS; MIR-200; FAMILY; ESOPHAGEAL CANCER; REPRESSORS ZEB1; FEEDBACK LOOP; TUMOR-GROWTH; ORAL-CANCER; EXPRESSION; ARK5;
D O I
10.18632/oncotarget.6972
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:8223 / 8239
页数:17
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