Insulin-like growth factor binding protein-5 (IGFBP-5) suppresses the tumorigenesis of head and neck squalmous cell carcinoma

被引:43
作者
Hung, P-S [1 ]
Kao, S-Y [1 ,2 ]
Shih, Y-H [1 ]
Chiou, S-H [1 ,3 ]
Liu, C-J [1 ,4 ]
Chang, K-W [1 ,3 ]
Lin, S-C [1 ]
机构
[1] Natl Yang Ming Univ, Sch Dent, Inst Oral Biol, Taipei, Taiwan
[2] Taipei Vet Gen Hosp, Dept Dent, Taipei, Taiwan
[3] Taipei Vet Gen Hosp, Dept Med Res & Educ, Taipei, Taiwan
[4] Mackay Mem Hosp, Dept Oral & Maxillofacial Surg, Taipei, Taiwan
关键词
carcinoma; IGF; IGFBP-5; keratinocyte; head and neck; tumourigenesis;
D O I
10.1002/path.2280
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Head and neck squamous cell carcinoma (HNSCC) is a global malignancy. The insulin-like growth factor (IGF) signalling axis plays a critical role in tumourigenesis. This study defined the clinical and functional roles of insulin-like growth factor binding protein-5 (IGFBP-5) in HNSCC. Down-regulation of IGFBP-5 mRNA expression was found during the progression from pre-cancer to HNSCC. The down-regulation in HNSCC was associated with a higher propensity to nodal metastasis. SAS and OECM-1 are HNSCC cells that do, or do not, express IGFBP-5, respectively. Recombinant IGFBP-5 reduced the proliferation of OECM-1 cells and this was exerted mainly through blockade of the IGF pathways. Either IGFBP-5 or IGF-I treatment alone promoted OECM-1 migration, but a combination of treatments generated antagonistic effects. Overexpression of IGFBP-5 reduced the proliferation and anchorage-independent growth of both OECM-1 and SAS cells. Conversely, knockdown of IGFBP-5 expression significantly induced the proliferation and anchorage-independent growth of SAS cells. It also induced the growth of xenografted SAS tumours. SAS transfectants that expressed mutant or truncated IGFBP-5, which lack IGF binding activity, exhibited significantly lower anchorage-independent growth than vector control. This suggests that IGFBP-5 possesses an IGF-independent suppressor function. The suppressive effects of IGFBP-5 on the tumourigenesis of HNSCC might be invaluable to future neoplastic intervention. Copyright (C) 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:368 / 376
页数:9
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