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Tissue-Engineering the Fibrous Pancreatic Tumour Stroma Capsule in 3D Tumouroids to Demonstrate Paclitaxel Response
by
Pape, Judith
, Uchegbu, Ijeoma F.
, Loizidou, Marilena
, Stamati, Katerina
, Schatzlein, Andreas G.
, Cheema, Umber
, Al Hosni, Rawiya
, Emberton, Mark
in
Cancer therapies
/ Cell Line, Tumor
/ Cell Proliferation
/ Chemotherapy
/ Collagen
/ Dose-Response Relationship, Drug
/ Drug dosages
/ Drug Resistance, Neoplasm
/ Drug testing
/ Extracellular matrix
/ Fluorescent Antibody Technique
/ Humans
/ Immunohistochemistry
/ Metabolism
/ Mutation
/ Paclitaxel - pharmacology
/ Paclitaxel - therapeutic use
/ Pancreatic cancer
/ Pancreatic Neoplasms - drug therapy
/ Pancreatic Neoplasms - pathology
/ Spheroids, Cellular
/ Stains & staining
/ Stromal Cells - drug effects
/ Stromal Cells - metabolism
/ Stromal Cells - pathology
/ Tissue Engineering
/ Tumor Cells, Cultured
/ Tumor Microenvironment - drug effects
2021
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Tissue-Engineering the Fibrous Pancreatic Tumour Stroma Capsule in 3D Tumouroids to Demonstrate Paclitaxel Response
by
Pape, Judith
, Uchegbu, Ijeoma F.
, Loizidou, Marilena
, Stamati, Katerina
, Schatzlein, Andreas G.
, Cheema, Umber
, Al Hosni, Rawiya
, Emberton, Mark
in
Cancer therapies
/ Cell Line, Tumor
/ Cell Proliferation
/ Chemotherapy
/ Collagen
/ Dose-Response Relationship, Drug
/ Drug dosages
/ Drug Resistance, Neoplasm
/ Drug testing
/ Extracellular matrix
/ Fluorescent Antibody Technique
/ Humans
/ Immunohistochemistry
/ Metabolism
/ Mutation
/ Paclitaxel - pharmacology
/ Paclitaxel - therapeutic use
/ Pancreatic cancer
/ Pancreatic Neoplasms - drug therapy
/ Pancreatic Neoplasms - pathology
/ Spheroids, Cellular
/ Stains & staining
/ Stromal Cells - drug effects
/ Stromal Cells - metabolism
/ Stromal Cells - pathology
/ Tissue Engineering
/ Tumor Cells, Cultured
/ Tumor Microenvironment - drug effects
2021
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Tissue-Engineering the Fibrous Pancreatic Tumour Stroma Capsule in 3D Tumouroids to Demonstrate Paclitaxel Response
by
Pape, Judith
, Uchegbu, Ijeoma F.
, Loizidou, Marilena
, Stamati, Katerina
, Schatzlein, Andreas G.
, Cheema, Umber
, Al Hosni, Rawiya
, Emberton, Mark
in
Cancer therapies
/ Cell Line, Tumor
/ Cell Proliferation
/ Chemotherapy
/ Collagen
/ Dose-Response Relationship, Drug
/ Drug dosages
/ Drug Resistance, Neoplasm
/ Drug testing
/ Extracellular matrix
/ Fluorescent Antibody Technique
/ Humans
/ Immunohistochemistry
/ Metabolism
/ Mutation
/ Paclitaxel - pharmacology
/ Paclitaxel - therapeutic use
/ Pancreatic cancer
/ Pancreatic Neoplasms - drug therapy
/ Pancreatic Neoplasms - pathology
/ Spheroids, Cellular
/ Stains & staining
/ Stromal Cells - drug effects
/ Stromal Cells - metabolism
/ Stromal Cells - pathology
/ Tissue Engineering
/ Tumor Cells, Cultured
/ Tumor Microenvironment - drug effects
2021
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Tissue-Engineering the Fibrous Pancreatic Tumour Stroma Capsule in 3D Tumouroids to Demonstrate Paclitaxel Response
Journal Article
Tissue-Engineering the Fibrous Pancreatic Tumour Stroma Capsule in 3D Tumouroids to Demonstrate Paclitaxel Response
2021
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Overview
Pancreatic cancer is a unique cancer in that up to 90% of its tumour mass is composed of a hypovascular and fibrotic stroma. This makes it extremely difficult for chemotherapies to be delivered into the core of the cancer mass. We tissue-engineered a biomimetic 3D pancreatic cancer (“tumouroid”) model comprised of a central artificial cancer mass (ACM), containing MIA Paca-2 cells, surrounded by a fibrotic stromal compartment. This stromal compartment had a higher concentration of collagen type I, fibronectin, laminin, and hyaluronic acid (HA) than the ACM. The incorporation of HA was validated with alcian blue staining. Response to paclitaxel was determined in 2D MIA Paca-2 cell cultures, the ACMs alone, and in simple and complex tumouroids, in order to demonstrate drug sensitivity within pancreatic tumouroids of increasing complexity. The results showed that MIA Paca-2 cells grew into the complex stroma and invaded as cell clusters with a maximum distance of 363.7 µm by day 21. In terms of drug response, the IC50 for paclitaxel for MIA Paca-2 cells increased from 0.819 nM in 2D to 3.02 nM in ACMs and to 5.87 nM and 3.803 nM in simple and complex tumouroids respectively, indicating that drug penetration may be significantly reduced in the latter. The results demonstrate the need for biomimetic models during initial drug testing and evaluation.
Publisher
MDPI AG,MDPI
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