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Multi-omics analysis based on 3D-bioprinted models innovates therapeutic target discovery of osteosarcoma
Current in vitro models for osteosarcoma investigation and drug screening, including two-dimensional (2D) cell culture and tumour spheroids (i.e. cancer stem-like cells), lack extracellular matrix (ECM). Therefore, results from traditional models may not reflect real pathological processes in genuin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971536/ https://www.ncbi.nlm.nih.gov/pubmed/35415297 http://dx.doi.org/10.1016/j.bioactmat.2022.03.029 |
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author | Lin, Yixuan Yang, Yiqi Yuan, Kai Yang, Shengbing Zhang, Shuhong Li, Hanjun Tang, Tingting |
author_facet | Lin, Yixuan Yang, Yiqi Yuan, Kai Yang, Shengbing Zhang, Shuhong Li, Hanjun Tang, Tingting |
author_sort | Lin, Yixuan |
collection | PubMed |
description | Current in vitro models for osteosarcoma investigation and drug screening, including two-dimensional (2D) cell culture and tumour spheroids (i.e. cancer stem-like cells), lack extracellular matrix (ECM). Therefore, results from traditional models may not reflect real pathological processes in genuine osteosarcoma histological structures. Here, we report a three-dimensional (3D) bioprinted osteosarcoma model (3DBPO) that contains osteosarcoma cells and shrouding ECM analogue in a 3D frame. Photo-crosslinkable bioinks composed of gelatine methacrylamide and hyaluronic acid methacrylate mimicked tumour ECM. We performed multi-omics analysis, including transcriptomics and DNA methylomics, to determine differences between the 3DBPO model and traditional models. Compared with 2D models and tumour spheroids, our 3DBPO model showed significant changes in cell cycle, metabolism, adherens junctions, and other pathways associated with epigenetic regulation. The 3DBPO model was more sensitive to therapies targeted to the autophagy pathway. We showed that simulating ECM yielded different osteosarcoma cell metabolic characteristics and drug sensitivity in the 3DBPO model compared with classical models. We suggest 3D printed osteosarcoma models can be used in osteosarcoma fundamental and translational research, which may contribute to novel therapeutic strategy discovery. |
format | Online Article Text |
id | pubmed-8971536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-89715362022-04-11 Multi-omics analysis based on 3D-bioprinted models innovates therapeutic target discovery of osteosarcoma Lin, Yixuan Yang, Yiqi Yuan, Kai Yang, Shengbing Zhang, Shuhong Li, Hanjun Tang, Tingting Bioact Mater Article Current in vitro models for osteosarcoma investigation and drug screening, including two-dimensional (2D) cell culture and tumour spheroids (i.e. cancer stem-like cells), lack extracellular matrix (ECM). Therefore, results from traditional models may not reflect real pathological processes in genuine osteosarcoma histological structures. Here, we report a three-dimensional (3D) bioprinted osteosarcoma model (3DBPO) that contains osteosarcoma cells and shrouding ECM analogue in a 3D frame. Photo-crosslinkable bioinks composed of gelatine methacrylamide and hyaluronic acid methacrylate mimicked tumour ECM. We performed multi-omics analysis, including transcriptomics and DNA methylomics, to determine differences between the 3DBPO model and traditional models. Compared with 2D models and tumour spheroids, our 3DBPO model showed significant changes in cell cycle, metabolism, adherens junctions, and other pathways associated with epigenetic regulation. The 3DBPO model was more sensitive to therapies targeted to the autophagy pathway. We showed that simulating ECM yielded different osteosarcoma cell metabolic characteristics and drug sensitivity in the 3DBPO model compared with classical models. We suggest 3D printed osteosarcoma models can be used in osteosarcoma fundamental and translational research, which may contribute to novel therapeutic strategy discovery. KeAi Publishing 2022-03-29 /pmc/articles/PMC8971536/ /pubmed/35415297 http://dx.doi.org/10.1016/j.bioactmat.2022.03.029 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Lin, Yixuan Yang, Yiqi Yuan, Kai Yang, Shengbing Zhang, Shuhong Li, Hanjun Tang, Tingting Multi-omics analysis based on 3D-bioprinted models innovates therapeutic target discovery of osteosarcoma |
title | Multi-omics analysis based on 3D-bioprinted models innovates therapeutic target discovery of osteosarcoma |
title_full | Multi-omics analysis based on 3D-bioprinted models innovates therapeutic target discovery of osteosarcoma |
title_fullStr | Multi-omics analysis based on 3D-bioprinted models innovates therapeutic target discovery of osteosarcoma |
title_full_unstemmed | Multi-omics analysis based on 3D-bioprinted models innovates therapeutic target discovery of osteosarcoma |
title_short | Multi-omics analysis based on 3D-bioprinted models innovates therapeutic target discovery of osteosarcoma |
title_sort | multi-omics analysis based on 3d-bioprinted models innovates therapeutic target discovery of osteosarcoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971536/ https://www.ncbi.nlm.nih.gov/pubmed/35415297 http://dx.doi.org/10.1016/j.bioactmat.2022.03.029 |
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