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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...

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Autores principales: Lin, Yixuan, Yang, Yiqi, Yuan, Kai, Yang, Shengbing, Zhang, Shuhong, Li, Hanjun, Tang, Tingting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
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.
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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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