Modeling Endothelialized Hepatic Tumor Microtissues for Drug Screening
Abstract Compared to various traditional 2D approaches, the scaffold‐based 3D tumor models have emerged as an effective strategy to investigate the complex mechanisms behind cancer progression and responses to drug treatments, by providing biomimetic extracellular matrix and stromal‐like microenviro...
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Online Access: | https://doi.org/10.1002/advs.202002002 |
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doaj-c432b0a6dc0748f0b2904c3f5e6e73922020-11-25T04:00:00ZengWileyAdvanced Science2198-38442020-11-01721n/an/a10.1002/advs.202002002Modeling Endothelialized Hepatic Tumor Microtissues for Drug ScreeningYing Wang0Ranjith Kumar Kankala1Jianting Zhang2Liuzhi Hao3Kai Zhu4Shibin Wang5Yu Shrike Zhang6Aizheng Chen7Institute of Biomaterials and Tissue Engineering Huaqiao University Xiamen 361021 P. R. ChinaInstitute of Biomaterials and Tissue Engineering Huaqiao University Xiamen 361021 P. R. ChinaInstitute of Biomaterials and Tissue Engineering Huaqiao University Xiamen 361021 P. R. ChinaInstitute of Biomaterials and Tissue Engineering Huaqiao University Xiamen 361021 P. R. ChinaDepartment of Cardiac Surgery Zhongshan Hospital Fudan University Shanghai 200032 P. R. ChinaInstitute of Biomaterials and Tissue Engineering Huaqiao University Xiamen 361021 P. R. ChinaDivision of Engineering in Medicine Brigham and Women's Hospital Department of Medicine Harvard Medical School Cambridge MA 02139 USAInstitute of Biomaterials and Tissue Engineering Huaqiao University Xiamen 361021 P. R. ChinaAbstract Compared to various traditional 2D approaches, the scaffold‐based 3D tumor models have emerged as an effective strategy to investigate the complex mechanisms behind cancer progression and responses to drug treatments, by providing biomimetic extracellular matrix and stromal‐like microenvironments including the vascular elements. Herein, the development of a 3D endothelialized hepatic tumor microtissue model based on the fusion of multicellular aggregates of human hepatocellular carcinoma cells and human umbilical vein endothelial cells cocultured in poly(lactic‐co‐glycolic acid)‐based porous microspheres (PLGA PMs) is reported. In contrast to the conventional 2D culture, the cells within the PLGA PMs exhibit significantly higher half‐maximal inhibitory concentration values against anticancer drugs, including doxorubicin and cisplatin. Furthermore, the feasibility of coculturing other cell types, such as fibroblasts (L929) and HepG2 cells, is investigated. Together, the findings emphasize the significance of engineered 3D hepatic tumor microtissue models using PLGA PM‐based multicellular aggregates for drug screening applications.https://doi.org/10.1002/advs.202002002anticancerdrug screeninghepatic modelsmulticellular tumor aggregatesvascularization |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ying Wang Ranjith Kumar Kankala Jianting Zhang Liuzhi Hao Kai Zhu Shibin Wang Yu Shrike Zhang Aizheng Chen |
spellingShingle |
Ying Wang Ranjith Kumar Kankala Jianting Zhang Liuzhi Hao Kai Zhu Shibin Wang Yu Shrike Zhang Aizheng Chen Modeling Endothelialized Hepatic Tumor Microtissues for Drug Screening Advanced Science anticancer drug screening hepatic models multicellular tumor aggregates vascularization |
author_facet |
Ying Wang Ranjith Kumar Kankala Jianting Zhang Liuzhi Hao Kai Zhu Shibin Wang Yu Shrike Zhang Aizheng Chen |
author_sort |
Ying Wang |
title |
Modeling Endothelialized Hepatic Tumor Microtissues for Drug Screening |
title_short |
Modeling Endothelialized Hepatic Tumor Microtissues for Drug Screening |
title_full |
Modeling Endothelialized Hepatic Tumor Microtissues for Drug Screening |
title_fullStr |
Modeling Endothelialized Hepatic Tumor Microtissues for Drug Screening |
title_full_unstemmed |
Modeling Endothelialized Hepatic Tumor Microtissues for Drug Screening |
title_sort |
modeling endothelialized hepatic tumor microtissues for drug screening |
publisher |
Wiley |
series |
Advanced Science |
issn |
2198-3844 |
publishDate |
2020-11-01 |
description |
Abstract Compared to various traditional 2D approaches, the scaffold‐based 3D tumor models have emerged as an effective strategy to investigate the complex mechanisms behind cancer progression and responses to drug treatments, by providing biomimetic extracellular matrix and stromal‐like microenvironments including the vascular elements. Herein, the development of a 3D endothelialized hepatic tumor microtissue model based on the fusion of multicellular aggregates of human hepatocellular carcinoma cells and human umbilical vein endothelial cells cocultured in poly(lactic‐co‐glycolic acid)‐based porous microspheres (PLGA PMs) is reported. In contrast to the conventional 2D culture, the cells within the PLGA PMs exhibit significantly higher half‐maximal inhibitory concentration values against anticancer drugs, including doxorubicin and cisplatin. Furthermore, the feasibility of coculturing other cell types, such as fibroblasts (L929) and HepG2 cells, is investigated. Together, the findings emphasize the significance of engineered 3D hepatic tumor microtissue models using PLGA PM‐based multicellular aggregates for drug screening applications. |
topic |
anticancer drug screening hepatic models multicellular tumor aggregates vascularization |
url |
https://doi.org/10.1002/advs.202002002 |
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