Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.804000
Title: Development of a 3D biomimetic tissue-engineered model of cancer
Author: Pape, Judith Maria
Awarding Body: UCL (University College London)
Current Institution: University College London (University of London)
Date of Award: 2020
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Abstract:
Introduction: Three dimensional (3D) models of cancer have been a major focus in advances to research discoveries toward cancer progression and the involvement of the cancer stroma. Next to extracellular matrix components such as hyaluronic acid (HA), cancer associated fibroblasts (CAFs) are highly differentiated and heterogenous cancer stromal cells that promote tumour growth, angiogenesis and matrix remodelling. Methods: We utilised a novel 3D in vitro model of colorectal (CRC) and pancreatic cancer, composed of an artificial cancer mass (ACM) with varying invasive propensities and a stromal compartment. We incorporated extracellular matrix components and six colorectal patient-derived CAF samples to study their differential effects. The chemotherapy drug paclitaxel was tested on 3D models of pancreatic cancer with increasing complexity. Results: The main finding was that the invasive nature of a cancer mass directly influenced the complexity of a developing vascular network. All network alignments were quantified and endothelial structures aligned along the chemotactic gradient formed by the CRC mass. CRC and pancreatic cancer invades as clusters and sheets in contrast to their non-cancerous counterparts. Using quantitative PCR, we demonstrated the key genes and active proteins responsible for this invasion. The addition of stromal fibroblasts and endothelial cells provided a biomimetic microenvironment which was reflected by the upregulation of invasive genes. CAFs enhanced the distance and surface area of the invasive cancer mass whilst inhibiting vascular-like network formation. Pancreatic cancer cells within a highly complex 3D model responded to paclitaxel and dose response curves could be established. Conclusion: These results support, within a biomimetic 3D, in vitro framework, the underlying gene pathways involved in cancer invasion and vascularisation. Furthermore, a complex model of pancreatic cancer was developed accounting for the large stromal proportion and used as a drug testing platform.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.804000  DOI: Not available
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