Insulin-like growth factor binding protein-3 inhibits migration of endometrial cancer cells

被引:11
作者
Gribben, Lujia [1 ]
Baxter, Robert C. [1 ]
Marsh, Deborah J. [1 ]
机构
[1] Univ Sydney, Royal N Shore Hosp, Hormones & Canc Div, Kolling Inst Med Res, St Leonards, NSW 2065, Australia
基金
澳大利亚研究理事会;
关键词
Endometrial cancer; IGFBP-3; PTEN; Migration; RETINOID-X-RECEPTOR; FACTOR-I; POSTMENOPAUSAL WOMEN; FACTOR BINDING-PROTEIN-3; SIGNALING PATHWAYS; PROSTATE-CANCER; SERUM-LEVELS; BARBED END; CARCINOMA; IGFBP-3;
D O I
10.1016/j.canlet.2011.11.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Cell migration and invasion leading to metastasis is a major cause of death from endometrial cancer (EC). We have shown that the rate of EC cell migration is inversely related to the level of insulin-like growth factor protein-3 (IGFBP-3). Down-regulation of IGFBP-3 by siRNA in EC cells accelerated migration without affecting proliferation and cells displayed a more migratory phenotype, with co-localization of migration-associated markers at the leading edge of cell membranes. Opposite effects were seen with either the addition of recombinant IGFBP-3 or overexpression of IGEBP-3. Cells with mutated PTEN had the highest IGFBP-3 expression and the slowest migration rates. This study demonstrates that endogenous IGEBP-3 modulates adhesion-migration dynamics in EC cells, implying that it may be important in regulating metastasis in this disease. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:41 / 48
页数:8
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