Interactions between human osteoblasts and prostate cancer cells in a novel 3D in vitro model

被引:58
|
作者
Sieh, Shirly [1 ]
Lubik, Amy A. [1 ,2 ]
Clements, Judith A. [1 ,2 ]
Nelson, Colleen C. [1 ,2 ]
Hutmacher, Dietmar W. [1 ]
机构
[1] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld 4001, Australia
[2] Princess Alexandra Hosp, Australian Prostate Canc Res Ctr Queensland, Woolloongabba, Qld, Australia
关键词
3D in vitro model; bone metastasis; co-culture; tissue engineering; prostate cancer; osteoblasts; ESTABLISHMENT; METASTASIS;
D O I
10.4161/org.6.3.12041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell-cell and cell-matrix interactions play a major role in tumor morphogenesis and cancer metastasis. Therefore, it is crucial to create a model with a biomimetic microenvironment that allows such interactions to fully represent the pathophysiology of a disease for an in vitro study. This is achievable by using three-dimensional (3D) models instead of conventional two-dimensional (2D) cultures with the aid of tissue engineering technology. We are now able to better address the complex intercellular interactions underlying prostate cancer (CaP) bone metastasis through such models. In this study, we assessed the interaction of CaP cells and human osteoblasts (hOBs) within a tissue engineered bone (TEB) construct. Consistent with other in vivo studies, our findings show that intercellular and CaP cell-bone matrix interactions lead to elevated levels of matrix metalloproteinases, steroidogenic enzymes and the CaP biomarker, prostate specific antigen (PSA); all associated with CaP metastasis. Hence, it highlights the physiological relevance of this model. We believe that this model will provide new insights for understanding of the previously poorly understood molecular mechanisms of bone metastasis, which will foster further translational studies, and ultimately offer a potential tool for drug screening.
引用
收藏
页码:181 / 188
页数:8
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