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A humanised tissue-engineered bone model allows species-specific breast cancer-related bone metastasis in vivo.

Authors :
Quent V
Taubenberger AV
Reichert JC
Martine LC
Clements JA
Hutmacher DW
Loessner D
Source :
Journal of tissue engineering and regenerative medicine [J Tissue Eng Regen Med] 2018 Feb; Vol. 12 (2), pp. 494-504. Date of Electronic Publication: 2017 Nov 29.
Publication Year :
2018

Abstract

Bone metastases frequently occur in the advanced stages of breast cancer. At this stage, the disease is deemed incurable. To date, the mechanisms of breast cancer-related metastasis to bone are poorly understood. This may be attributed to the lack of appropriate animal models to investigate the complex cancer cell-bone interactions. In this study, two established tissue-engineered bone constructs (TEBCs) were applied to a breast cancer-related metastasis model. A cylindrical medical-grade polycaprolactone-tricalcium phosphate scaffold produced by fused deposition modelling (scaffold 1) was compared with a tubular calcium phosphate-coated polycaprolactone scaffold fabricated by solution electrospinning (scaffold 2) for their potential to generate ectopic humanised bone in NOD/SCID mice. While scaffold 1 was found not suitable to generate a sufficient amount of ectopic bone tissue due to poor ectopic integration, scaffold 2 showed excellent integration into the host tissue, leading to bone formation. To mimic breast cancer cell colonisation to the bone, MDA-MB-231, SUM1315, and MDA-MB-231BO breast cancer cells were cultured in polyethylene glycol-based hydrogels and implanted adjacent to the TEBCs. Histological analysis indicated that the breast cancer cells induced an osteoclastic reaction in the TEBCs, demonstrating analogies to breast cancer-related bone metastasis seen in patients.<br /> (Copyright © 2017 John Wiley & Sons, Ltd.)

Details

Language :
English
ISSN :
1932-7005
Volume :
12
Issue :
2
Database :
MEDLINE
Journal :
Journal of tissue engineering and regenerative medicine
Publication Type :
Academic Journal
Accession number :
28714574
Full Text :
https://doi.org/10.1002/term.2517