Modeling the human bone–tumor niche: reducing and replacing the need for animal data
Bone is the most common site for cancer metastasis. Understanding the interactions within the complex, heterogeneous bone–tumor microenvironment is essential for the development of new therapeutics. Various animal models of tumor‐induced bone disease are routinely used to provide valuable informatio...
| Main Authors: | , , |
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| Format: | Journal article |
| Language: | English |
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Wiley
2020
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| _version_ | 1797089393107795968 |
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| author | Rao, SR Edwards, CM Edwards, JR |
| author_facet | Rao, SR Edwards, CM Edwards, JR |
| author_sort | Rao, SR |
| collection | OXFORD |
| description | Bone is the most common site for cancer metastasis. Understanding the interactions within the complex, heterogeneous bone–tumor microenvironment is essential for the development of new therapeutics. Various animal models of tumor‐induced bone disease are routinely used to provide valuable information on the relationship between cancer cells and the skeleton. However, new model systems exist that offer an alternative approach to the use of animals and might more accurately reveal the cellular interactions occurring within the human bone–tumor niche. This review highlights replacement models that mimic the bone microenvironment and where cancer metastases and tumor growth might be assessed alongside bone turnover. Such culture models include the use of calcified regions of animal tissue and scaffolds made from bone mineral hydroxyapatite, synthetic polymers that can be manipulated during manufacture to create structures resembling trabecular bone surfaces, gel composites that can be modified for stiffness and porosity to resemble conditions in the tumor–bone microenvironment. Possibly the most accurate model system involves the use of fresh human bone samples, which can be cultured ex vivo in the presence of human tumor cells and demonstrate similar cancer cell–bone cell interactions as described in vivo. In addition, the use of mathematical modeling and computational biology approaches provide an alternative to preliminary animal testing. The use of such models offers the capacity to mimic significant elements of the human bone–tumor environment, and complement, refine, or replace the use of preclinical models.
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| first_indexed | 2024-03-07T03:03:31Z |
| format | Journal article |
| id | oxford-uuid:b1bdd190-89f2-43f4-971c-35e8f1b39106 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T03:03:31Z |
| publishDate | 2020 |
| publisher | Wiley |
| record_format | dspace |
| spelling | oxford-uuid:b1bdd190-89f2-43f4-971c-35e8f1b391062022-03-27T04:06:22ZModeling the human bone–tumor niche: reducing and replacing the need for animal dataJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:b1bdd190-89f2-43f4-971c-35e8f1b39106EnglishSymplectic ElementsWiley2020Rao, SREdwards, CMEdwards, JRBone is the most common site for cancer metastasis. Understanding the interactions within the complex, heterogeneous bone–tumor microenvironment is essential for the development of new therapeutics. Various animal models of tumor‐induced bone disease are routinely used to provide valuable information on the relationship between cancer cells and the skeleton. However, new model systems exist that offer an alternative approach to the use of animals and might more accurately reveal the cellular interactions occurring within the human bone–tumor niche. This review highlights replacement models that mimic the bone microenvironment and where cancer metastases and tumor growth might be assessed alongside bone turnover. Such culture models include the use of calcified regions of animal tissue and scaffolds made from bone mineral hydroxyapatite, synthetic polymers that can be manipulated during manufacture to create structures resembling trabecular bone surfaces, gel composites that can be modified for stiffness and porosity to resemble conditions in the tumor–bone microenvironment. Possibly the most accurate model system involves the use of fresh human bone samples, which can be cultured ex vivo in the presence of human tumor cells and demonstrate similar cancer cell–bone cell interactions as described in vivo. In addition, the use of mathematical modeling and computational biology approaches provide an alternative to preliminary animal testing. The use of such models offers the capacity to mimic significant elements of the human bone–tumor environment, and complement, refine, or replace the use of preclinical models. |
| spellingShingle | Rao, SR Edwards, CM Edwards, JR Modeling the human bone–tumor niche: reducing and replacing the need for animal data |
| title | Modeling the human bone–tumor niche: reducing and replacing the need for animal data |
| title_full | Modeling the human bone–tumor niche: reducing and replacing the need for animal data |
| title_fullStr | Modeling the human bone–tumor niche: reducing and replacing the need for animal data |
| title_full_unstemmed | Modeling the human bone–tumor niche: reducing and replacing the need for animal data |
| title_short | Modeling the human bone–tumor niche: reducing and replacing the need for animal data |
| title_sort | modeling the human bone tumor niche reducing and replacing the need for animal data |
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