Peptide-protein coassembling matrices as a biomimetic 3D model of ovarian cancer

Bioengineered three-dimensional (3D) matrices expand our experimental repertoire to study tumor growth and progression in a biologically relevant, yet controlled, manner. Here, we used peptide amphiphiles (PAs) to coassemble with and organize extracellular matrix (ECM) proteins producing tunable 3D...

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Main Authors: Hedegaard, Clara Louise, Redondo-Gómez, Carlos, Tan, Bee Yi, Ng, Kee Woei, Loessner, Daniela, Mata, Alvaro
Other Authors: School of Materials Science and Engineering
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/145362
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1453622023-07-14T15:47:29Z Peptide-protein coassembling matrices as a biomimetic 3D model of ovarian cancer Hedegaard, Clara Louise Redondo-Gómez, Carlos Tan, Bee Yi Ng, Kee Woei Loessner, Daniela Mata, Alvaro School of Materials Science and Engineering Nanyang Environment and Water Research Institute Engineering::Bioengineering Biomimetics Cell Culture Bioengineered three-dimensional (3D) matrices expand our experimental repertoire to study tumor growth and progression in a biologically relevant, yet controlled, manner. Here, we used peptide amphiphiles (PAs) to coassemble with and organize extracellular matrix (ECM) proteins producing tunable 3D models of the tumor microenvironment. The matrix was designed to mimic physical and biomolecular features of tumors present in patients. We included specific epitopes, PA nanofibers, and ECM macromolecules for the 3D culture of human ovarian cancer, endothelial, and mesenchymal stem cells. The multicellular constructs supported the formation of tumor spheroids with extensive F-actin networks surrounding the spheroids, enabling cell-cell communication, and comparative cell-matrix interactions and encapsulation response to those observed in Matrigel. We conducted a proof-of-concept study with clinically used chemotherapeutics to validate the functionality of the multicellular constructs. Our study demonstrates that peptide-protein coassembling matrices serve as a defined model of the multicellular tumor microenvironment of primary ovarian tumors. Published version 2020-12-18T05:46:18Z 2020-12-18T05:46:18Z 2020 Journal Article Hedegaard, C. L., Redondo-Gómez, C., Tan, B. Y., Ng, K. W., Loessner, D., & Mata, A. (2020). Peptide-protein coassembling matrices as a biomimetic 3D model of ovarian cancer. Science Advances, 6(40), eabb3298-. doi:10.1126/sciadv.abb3298 2375-2548 https://hdl.handle.net/10356/145362 10.1126/sciadv.abb3298 33008910 40 6 en Science Advances © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Bioengineering
Biomimetics
Cell Culture
spellingShingle Engineering::Bioengineering
Biomimetics
Cell Culture
Hedegaard, Clara Louise
Redondo-Gómez, Carlos
Tan, Bee Yi
Ng, Kee Woei
Loessner, Daniela
Mata, Alvaro
Peptide-protein coassembling matrices as a biomimetic 3D model of ovarian cancer
description Bioengineered three-dimensional (3D) matrices expand our experimental repertoire to study tumor growth and progression in a biologically relevant, yet controlled, manner. Here, we used peptide amphiphiles (PAs) to coassemble with and organize extracellular matrix (ECM) proteins producing tunable 3D models of the tumor microenvironment. The matrix was designed to mimic physical and biomolecular features of tumors present in patients. We included specific epitopes, PA nanofibers, and ECM macromolecules for the 3D culture of human ovarian cancer, endothelial, and mesenchymal stem cells. The multicellular constructs supported the formation of tumor spheroids with extensive F-actin networks surrounding the spheroids, enabling cell-cell communication, and comparative cell-matrix interactions and encapsulation response to those observed in Matrigel. We conducted a proof-of-concept study with clinically used chemotherapeutics to validate the functionality of the multicellular constructs. Our study demonstrates that peptide-protein coassembling matrices serve as a defined model of the multicellular tumor microenvironment of primary ovarian tumors.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
Hedegaard, Clara Louise
Redondo-Gómez, Carlos
Tan, Bee Yi
Ng, Kee Woei
Loessner, Daniela
Mata, Alvaro
format Article
author Hedegaard, Clara Louise
Redondo-Gómez, Carlos
Tan, Bee Yi
Ng, Kee Woei
Loessner, Daniela
Mata, Alvaro
author_sort Hedegaard, Clara Louise
title Peptide-protein coassembling matrices as a biomimetic 3D model of ovarian cancer
title_short Peptide-protein coassembling matrices as a biomimetic 3D model of ovarian cancer
title_full Peptide-protein coassembling matrices as a biomimetic 3D model of ovarian cancer
title_fullStr Peptide-protein coassembling matrices as a biomimetic 3D model of ovarian cancer
title_full_unstemmed Peptide-protein coassembling matrices as a biomimetic 3D model of ovarian cancer
title_sort peptide-protein coassembling matrices as a biomimetic 3d model of ovarian cancer
publishDate 2020
url https://hdl.handle.net/10356/145362
_version_ 1772825395796639744