The effect of bone morphogenetic protein-2 on osteosarcoma metastasis

被引:18
|
作者
Gill, Jonathan [1 ]
Connolly, Patrick [1 ]
Roth, Michael [1 ]
Chung, So Hak [2 ]
Zhang, Wendong [1 ]
Piperdi, Sajida [1 ]
Hoang, Bang [3 ]
Yang, Rui [3 ]
Guzik, Hillary [4 ]
Morris, Jonathan [3 ]
Gorlick, Richard [3 ,5 ]
Geller, David S. [1 ,3 ]
机构
[1] Childrens Hosp Montefiore, Div Pediat Hematol Oncol & Blood & Marrow Cell Tr, Albert Einstein Coll Med, Bronx, NY 10467 USA
[2] Kosin Univ, Coll Med, Busan, South Korea
[3] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Orthopaed Surg, Bronx, NY 10467 USA
[4] Albert Einstein Coll Med, Analyt Imaging Facil, Bronx, NY 10467 USA
[5] Albert Einstein Coll Med, Dept Mol Pharmacol, Bronx, NY 10467 USA
来源
PLOS ONE | 2017年 / 12卷 / 03期
关键词
STEM-CELLS; GROWTH; DIFFERENTIATION; EXPRESSION; RECEPTORS; ALLOGRAFT; SURGERY; SALVAGE; BMPS;
D O I
10.1371/journal.pone.0173322
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Purpose Bone Morphogenetic Protein-2 (BMP-2) may offer the potential to enhance allograft-host osseous union in limb-salvage surgery following osteosarcoma resection. However, there is concern regarding the effect of locally applied BMP-2 on tumor recurrence and metastasis. The purpose of this project was to evaluate the effect of exogenous BMP-2 on osteosarcoma migration and invasion across a panel of tumor cell lines in vitro and to characterize the effect of BMP-2 on pulmonary osteosarcoma metastasis within a xenograft model. Experimental design The effect of BMP-2 on in vitro tumor growth and development was assessed across multiple standard and patient-derived xenograft osteosarcoma cell lines. Tumor migration capacity, invasion, and cell proliferation were characterized. In addition, the effect on metastasis was measured using a xenograft model following tail-vein injection. The effect of exogenous BMP-2 on the development of metastases was measured following both single and multiple BMP-2 administrations. Results There was no significant difference in migration capacity, invasion, or cell proliferation between the BMP-2 treated and the untreated osteosarcoma cell lines. There was no significant difference in pulmonary metastases between either the single-dose or multi-dose BMP-2 treated animals and the untreated control animals. Conclusions In the model systems tested, the addition of BMP-2 does not increase osteosarcoma proliferation, migration, invasion, or metastasis to the lungs.
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页数:13
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