Polyurethane foam scaffold as in vitro model for breast cancer bone metastasis

被引:53
作者
Angeloni, Valentina [1 ]
Contessi, Nicola [2 ,3 ]
De Marco, Cinzia [1 ]
Bertoldi, Serena [2 ,3 ]
Tanzi, Maria Cristina [3 ]
Daidone, Maria Grazia [1 ]
Fare, Silvia [2 ,3 ]
机构
[1] Fdn IRCCS, Ist Nazl Tumori, Via Amedeo 42, I-20133 Milan, Italy
[2] Politecn Milan, Dept Chem Mat & Chem Engn G Natta, Piazza Leonardo da Vinci 32, I-20133 Milan, Italy
[3] Politecn Milan, Natl Consortium Mat Sci & Technol, INSTM, Local Unit, Piazza Leonardo da Vinci 32, I-20133 Milan, Italy
关键词
3D in vitro culture; Breast cancer; Bone metastasis model; Polyurethane foam; MOUSE MODEL; SKELETAL METASTASES; XENOGRAFT MODEL; TUMOR-GROWTH; CELLS; MECHANISMS; MICROENVIRONMENT; PROGRESSION; MIGRATION; SURVIVAL;
D O I
10.1016/j.actbio.2017.09.017
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Breast cancer (BC) represents the most incident cancer case in women (29%), with high mortality rate. Bone metastasis occurs in 20-50% cases and, despite advances in BC research, the interactions between tumor cells and the metastatic microenvironment are still poorly understood. In vitro 3D models gained great interest in cancer research, thanks to the reproducibility, the 3D spatial cues and associated low costs, compared to in vivo and 2D in vitro models. In this study, we investigated the suitability of a poly-ether-urethane (PU) foam as 3D in vitro model to study the interactions between BC tumor initiating cells and the bone microenvironment. PU foam open porosity (>70%) appeared suitable to mimic trabecular bone structure. The PU foam showed good mechanical properties under cyclic compression (E = 69-109 kPa), even if lower than human trabecular bone. The scaffold supported osteoblast SAOS-2 cell line proliferation, with no cytotoxic effects. Human adipose derived stem cells (ADSC) were cultured and differentiated into osteoblast lineage on the PU foam, as shown by alizarin red staining and RT-PCR, thus offering a bone biomimetic microenvironment to the further co-culture with BC derived tumor-initiating cells (MCFS). Tumor aggregates were observed after three weeks of co-culture by ecadherin staining and SEM; modification in CaP distribution was identified by SEM-EDX and associated to the presence of tumor cells. In conclusion, we demonstrated the suitability of the PU foam to reproduce a bone biomimetic microenvironment, useful for the co-culture of human osteoblasts/BC tumor-initiating cells and to investigate their interaction. Statement of significance 3D in vitro models represent an outstanding alternative in the study of tumor metastases development, compared to traditional 2D in vitro cultures, which oversimplify the 3D tissue microenvironment, and in vivo studies, affected by low reproducibility and ethical issues. Several scaffold-based 3D in vitro models have been proposed to recapitulate the development of metastases in different body sites but, still, the crucial challenge is to correctly mimic the tissue to be modelled in terms of physical, mechanical and biological properties. Here, we prove the suitability of a porous polyurethane foam, synthesized using an appropriate formulaton, in mimicking the bone tissue microenvironment and in reproducing the metastatic colonization derived from human breast cancer, particularly evidencing the devastating effects on the bone extracellular matrix caused by metastatic spreading. (C) 2017 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:306 / 316
页数:11
相关论文
共 60 条
[1]   Biology of breast cancer bone metastasis [J].
Akhtari, Mojtaba ;
Mansuri, Junaid ;
Newman, Kam A. ;
Guise, Theresa M. ;
Seth, Prem .
CANCER BIOLOGY & THERAPY, 2008, 7 (01) :3-9
[2]   Implications of stemness-related signaling pathways in breast cancer response to therapy [J].
Angeloni, Valentina ;
Tiberio, Paola ;
Appierto, Valentina ;
Daidone, Maria Grazia .
SEMINARS IN CANCER BIOLOGY, 2015, 31 :43-51
[3]   Direct but not indirect co-culture with osteogenically differentiated human bone marrow stromal cells increases RANKL/OPG ratio in human breast cancer cells generating bone metastases [J].
Arrigoni, Chiara ;
De Luca, Paola ;
Gilardi, Mara ;
Previdi, Sara ;
Broggini, Massimo ;
Moretti, Matteo .
MOLECULAR CANCER, 2014, 13
[4]   Ability of polyurethane foams to support placenta-derived cell adhesion and osteogenic differentiation: preliminary results [J].
Bertoldi, S. ;
Fare, S. ;
Denegri, M. ;
Rossi, D. ;
Haugen, H. J. ;
Parolini, O. ;
Tanzi, M. C. .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 2010, 21 (03) :1005-1011
[5]   Recent advances in bone tissue engineering scaffolds [J].
Bose, Susmita ;
Roy, Mangal ;
Bandyopadhyay, Amit .
TRENDS IN BIOTECHNOLOGY, 2012, 30 (10) :546-554
[6]   Inhibition of RANKL blocks skeletal tumor progression and improves survival in a mouse model of breast cancer bone metastasis [J].
Canon, Jude R. ;
Roudier, Martine ;
Bryant, Rebecca ;
Morony, Sean ;
Stolina, Marina ;
Kostenuik, Paul J. ;
Dougall, William C. .
CLINICAL & EXPERIMENTAL METASTASIS, 2008, 25 (02) :119-129
[7]   Dissemination and growth of cancer cells in metastatic sites [J].
Chambers, AF ;
Groom, AC ;
MacDonald, IC .
NATURE REVIEWS CANCER, 2002, 2 (08) :563-572
[8]   Cytokines in osteoblast-conditioned medium promote the migration of breast cancer cells [J].
Chen, Xiaojia ;
Lu, Jia ;
Ji, Yuhua ;
Hong, An ;
Xie, Qiuling .
TUMOR BIOLOGY, 2014, 35 (01) :791-798
[9]   Breast cancer metastasis to the bone: mechanisms of bone loss [J].
Chen, Yu-Chi ;
Sosnoski, Donna M. ;
Mastro, Andrea M. .
BREAST CANCER RESEARCH, 2010, 12 (06)
[10]   The Role of Cancer Stem Cells in the Organ Tropism of Breast Cancer Metastasis: A Mechanistic Balance between the "Seed" and the "Soil"? [J].
Chu, Jenny E. ;
Allan, Alison L. .
INTERNATIONAL JOURNAL OF BREAST CANCER, 2012, 2012