The impact of bone morphogenetic protein 4 (BMP4) on breast cancer metastasis in a mouse xenograft model

被引:25
|
作者
Ampuja, M. [1 ]
Alarmo, E. L. [1 ]
Owens, P. [2 ]
Havunen, R. [1 ]
Gorska, A. E. [2 ]
Moses, H. L. [2 ]
Kallioniemi, A. [1 ]
机构
[1] Univ Tampere, BioMediTech, FIN-33101 Tampere, Finland
[2] Vanderbilt Univ, Vanderbilt Ingram Canc Ctr, Dept Canc Biol, 221 Kirkland Hall, Nashville, TN 37235 USA
关键词
Bone morphogenetic protein; BMP4; Breast cancer; In vivo metastasis model; Bioluminescence imaging; CELLS; SUPPRESSES; ACTIVATION; REGULATOR; MIGRATION; INVASION; PROSTATE; GROWTH; DIFFERENTIATION; PROLIFERATION;
D O I
10.1016/j.canlet.2016.03.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Bone morphogenetic protein 4 (BMP4) is a key regulator of cell proliferation and differentiation. In breast cancer cells, BMP4 has been shown to reduce proliferation in vitro and interestingly, in some cases, also to induce migration and invasion. Here we investigated whether BMP4 influences breast cancer metastasis formation by using a xenograft mouse model. MDA-MB-231 breast cancer cells were injected intracardially into mice and metastasis formation was monitored using bioluminescence imaging. Mice treated with BMP4 developed metastases slightly earlier as compared to control animals but the overall number of metastases was similar in both groups (13 in the BMP4 group vs. 12 in controls). In BMP4treated mice, bone metastases were more common (10 vs. 7) but adrenal gland metastases were less frequent (1 vs. 5) than in controls. Immunostaining revealed no differences in signaling activation, proliferation rate, blood vessel formation, EMT markers or the number of cancer -associated fibroblasts between the treatment groups. In conclusion, BMP4 caused a trend towards accelerated metastasis formation, especially in bone. More work is needed to uncover the long-term effects of BMP4 and the clinical relevance of these findings. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:238 / 244
页数:7
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