Lipocalin 2 prevents oral cancer metastasis through carbonic anhydrase IX inhibition and is associated with favourable prognosis

被引:63
作者
Lin, Chiao-Wen [1 ,2 ]
Yang, Wei-En [3 ]
Lee, Wei-Jiunn [4 ]
Hua, Kuo-Tai [5 ]
Hsieh, Feng-Koo [6 ]
Hsiao, Michael [7 ]
Chen, Chia-Cheng [8 ]
Chow, Jyh-Ming [9 ]
Chen, Mu-Kuan [3 ,10 ]
Yang, Shun-Fa [3 ,11 ]
Chien, Ming-Hsien [4 ,12 ]
机构
[1] Chung Shan Med Univ, Inst Oral Sci, Taichung 40201, Taiwan
[2] Chung Shan Med Univ Hosp, Dept Dent, Taichung 40201, Taiwan
[3] Chung Shan Med Univ, Inst Med, Taichung 40201, Taiwan
[4] Taipei Med Univ, Wan Fang Hosp, Dept Med Res, Taipei 116, Taiwan
[5] Natl Taiwan Univ, Grad Inst Toxicol, Coll Med, Taipei 10051, Taiwan
[6] Univ Munich, Dept Surg, Expt Surg & Regenerat Med, D-80539 Munich, Germany
[7] Acad Sinica, Genom Res Ctr, Taipei 115, Taiwan
[8] Shin Kong Mem Hosp, Div Oral & Maxillofacial Surg, Dept Dent, Taipei 111, Taiwan
[9] Taipei Med Univ, Wan Fang Hosp, Dept Internal Med, Taipei 116, Taiwan
[10] Changhua Christian Hosp, Dept Otorhinolaryngol Head & Neck Surg, Changhua 505, Taiwan
[11] Chung Shan Med Univ Hosp, Dept Med Res, Taichung 40201, Taiwan
[12] Taipei Med Univ, Grad Inst Clin Med, Taipei 110, Taiwan
关键词
GELATINASE-ASSOCIATED LIPOCALIN; SQUAMOUS-CELL CARCINOMA; INVASION; GROWTH; NGAL; SUPPRESSES; EXPRESSION; MOTILITY; COMPLEX; BREAST;
D O I
10.1093/carcin/bgw050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Our study elucidated the clinical and prognostic significance of LCN2 in OSCC among the Taiwanese population. Moreover, we observed that LCN2 suppresses cell motility by downregulating CAIX protein level via HIF-1 alpha-mediated transcriptional regulation and miR-4505-mediated post-transcriptional regulation.Lipocalin 2 (LCN2), a secreted glycoprotein, is up- or downregulated in different human cancers. At present, the functional role of LCN2 in the progression of oral squamous cell carcinoma (OSCC), which accounts for most head and neck cancers, remains poorly understood, particularly with respect to its involvement in invasion and metastasis. In this study, we observed that LCN2 expression decreased in patients with OSCC and lymph node metastasis compared with that in patients without metastasis. A higher LCN2 expression correlated with the survival of patients with OSCC. Furthermore, LCN2 overexpression in OSCC cells reduced in vitro migration and invasion and in vivo metastasis, whereas its silencing induced an increase in cell motility. Mechanistically, LCN2 inhibited the cell motility of OSCC cells through hypoxia-inducible factor (HIF)-1 alpha-dependent transcriptional inhibition of the carbonic anhydrase IX (CAIX). CAIX overexpression relieved the migration inhibition imposed by LCN2 overexpression in OSCC cells. Moreover, a microRNA (miR) analysis revealed that LCN2 can suppress CAIX expression and cell migration through miR-4505 induction. Examination of tumour tissues from patients with OSCC and OSCC-transplanted mice revealed an inverse correlation between LCN2 and CAIX expression. Furthermore, patients with LCN2(strong)/CAIX(weak) revealed the lowest frequency of lymph node metastasis and the longest survival. Our findings suggest that LCN2 suppresses tumour metastasis by targeting the transcriptional and post-transcriptional regulation of CAIX in OSCC cells. LCN2 overexpression may be a novel OSCC treatment strategy and a useful biomarker for predicting OSCC progression.
引用
收藏
页码:712 / 722
页数:11
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