Abstract

Simple SummaryBreast cancer commonly migrates to the skeleton. Once patients have breast cancer in their bones, their quality of life is poor. Research has shown that the environment and structure of bone helps support metastatic breast cancer cell growth. Current models used in laboratories to study breast cancer that has migrated to bone do not include all the components of what happens in the human body. This is because technology in the past was limiting. Now, however, a new technology exists, called three-dimensional (3D) bioprinting, that “prints” living cells in geometries like the ones within the human body, to replicate a more realistic environment. In cancer research, 3D bioprinting allows researchers to more closely replicate events that occur when cancer cells migrate from a primary location to a secondary site, as well as model events in the environment of the secondary site. 3D bioprinting may also be used instead of animal models in some cases, and may speed up new drug discovery for cancer treatment.Breast cancer commonly metastasizes to bone, resulting in osteolytic lesions and poor patient quality of life. The bone extracellular matrix (ECM) plays a critical role in cancer cell metastasis by means of the physical and biochemical cues it provides to support cellular crosstalk. Current two-dimensional in-vitro models lack the spatial and biochemical complexities of the native ECM and do not fully recapitulate crosstalk that occurs between the tumor and endogenous stromal cells. Engineered models such as bone-on-a-chip, extramedullary bone, and bioreactors are presently used to model cellular crosstalk and bone–tumor cell interactions, but fall short of providing a bone-biomimetic microenvironment. Three-dimensional bioprinting allows for the deposition of biocompatible materials and living cells in complex architectures, as well as provides a means to better replicate biological tissue niches in-vitro. In cancer research specifically, 3D constructs have been instrumental in seminal work modeling cancer cell dissemination to bone and bone–tumor cell crosstalk in the skeleton. Furthermore, the use of biocompatible materials, such as hydroxyapatite, allows for printing of bone-like microenvironments with the ability to be implanted and studied in in-vivo animal models. Moreover, the use of bioprinted models could drive the development of novel cancer therapies and drug delivery vehicles.

Highlights

  • Bone is a unique organ that provides, among other things, structural support and protection for the body

  • The vascular sinusoids are the main entry point for disseminated tumor cells into the bones, with the majority of metastases occurring at the ends of long bones, including the femur, where there is a high rate of metabolic activity due to bone turnover by the osteoblasts and osteoclasts

  • These results suggest that the inhibition of sclerostin and/or inhibitors of DKK1 may be promising tools to promote osteoblast activity, leading to increased subsequent bone deposition in multiple myeloma bone disease

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Summary

Introduction

Bone is a unique organ that provides, among other things, structural support and protection for the body. The normal breast epithelial cells behaved to tumor cells when grown in 2D cultures [19] Such models inadequately represent the spatial, biochemical, and mechanical complexities of the native 3D tumor microenvironment, severely limiting their interpretation in the study of metastatic disease to the bone. Recognizing these shortcomings, investigators are developing 3D bone microenvironments such as bioreactors [20,21,22,23,24,25,26], scaffolds [27,28], extramedullary bone [29,30], and bone-on-a-chip [31,32] models for metastatic cancer research Such novel systems allow for more relevant material composition and spatial relationships among cells and, in some cases, provide similar mechanical forces. As a result of these and other advantages, 3D bioprinting has the potential to elevate into the generation current models in cancer research that mimic the bone–tumor niche

Gross Anatomy of Bone and Bone Physiology
Bone Remodeling during Disease
Bone Is a Favored Site of Cancer Metastasis
Breast Cancer Cells Preferentially Metastasize to Bone
Multiple Myeloma Metastases to the Bone
Prostate Cancer Colonization of the Skeleton
Lung Cancer Metastasizes to the Skeleton
Model Systems for Early Cancer Cell Dissemination to Bone
In-Vivo Models of Cancer Metastasis to Bone
Bioprinting Techniques
Bioinks
Applications of Bioprinting in Cancer
Bioprinted Models for Breast Cancer Metastasis
Findings
Conclusions andbioprinting
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