Full metadata
Title
Hydrogel Facilitated Melanoma Cell-Macrophage Co-culture Tumor Microenvironments
Description
Cellular models have been the backbone of models for drug therapeutics, discovery, or diagnostics, and for modeling a tumor microenvironment to understand the proliferation, migration, invasion, dormancy, angiogenesis, Conventional two-dimensional (2D) cell culture models are used because of the cost-effectiveness compared to animal models. But these models fail to mimic the cellular phenotype of a three-dimensional (3D) microenvironment. As a result, it is important to develop a 3D model that predicts cellular behaviors and their interaction with neighboring cells and extracellular matrix (ECM) in a more realistic setting. Various 3D cell culture methods have been employed to generate spheroids, in vitro, but most of these platforms face drawbacks such as spheroid size heterogeneity, low yield, use of specialized instruments etc. The hydrogel platform mentioned here was able to solve all the previous problems and can create a novel 3D tumor microenvironment. This thesis is focused on developing an in-vitro 3D model which can modulate the tumor microenvironment consisting of cancer cells and macrophages and how the Amikagel platform modulated the macrophage phenotype is discussed in detail here. This platform can be an ideal platform for macrophage phenotype modulation.
Date Created
2023
Contributors
- Chowdhury, Trishita (Author)
- Rege, Kaushal (Thesis advisor)
- Acharya, Abhinav (Committee member)
- Khalifehzadeh, Layla (Committee member)
- Arizona State University (Publisher)
Topical Subject
Resource Type
Extent
58 pages
Language
eng
Copyright Statement
In Copyright
Primary Member of
Peer-reviewed
No
Open Access
No
Handle
https://hdl.handle.net/2286/R.2.N.189267
Level of coding
minimal
Cataloging Standards
Note
Partial requirement for: M.S., Arizona State University, 2023
Field of study: Chemical Engineering
System Created
- 2023-08-28 04:54:49
System Modified
- 2023-08-28 04:54:53
- 1 year 3 months ago
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