3DPROSEEDTM StromaLineTM Collection
Our focus on the tumor-stroma interactions
3DProSeed ® is the ideal hydrogel platform to study the interactions between tumor cells and a model of the surrounding tumor stromal microenvironment. The fate of malignant cancer cells is influenced by a multitude of cells (fibroblasts and other mesenchymal supporting cells, endothelial and immune cells), soluble factors and matrix proteins surrounding them.
Our new 3DProSeed ® StromaLine ® is an attractive collection of pre-developed and well characterized stromal models ideal for tumor-stroma interaction studies. The ability to build a synthetic model of the stromal microenvironment in a high-content screening-compatible manner enables new discoveries in oncology. Anti-cancer drug screenings can be conducted in the presence of the stromal compartment with minimal adaptation efforts.
The key unique advantages of the StromaLine
3DProSeed 96-well imaging plate format with pre-casted hydrogels. No need for hydrogel assembly steps (visit 3DProSeed page for the technical details).
Pre-developed and guaranteed to be assay-ready - delivered with own pretested cells, media and characterization reagents from a single source - Ectica Technologies.
The hydrogel is synthetic - free from animal derived components. All proteins deposited in the hydrogel are endogenously deposited by cells resulting in highly characterized stromal models for tumor interaction studies.
The StromaLineTM Collection
MESENCHYMAL STROMAL CELLS (MSCs) MATRIX
We offer the 3DProSeed Stromaline with our pre-developed and characterized mesenchymal stromal matrix originating from adipose tissue or bone marrow MSCs. MSCs are multipotent stromal cells that are involved in a multitude of physiological and pathological conditions, including tissue regeneration, immune defence mechanisms, paracrine signalling, and tumour growth and metastasis. MSCs are also widely used in basic research, either to understand their biology or as a model system to investigate the role of the stroma in regulating tissue-specific cell behaviour. Of particular interest is the ability of MSCs to deposit and remodel extracellular matrix components, to secrete a variety of signalling molecules, and to participate in crosstalk with tissue-specific cells.
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BONE MARROW VASCULAR NICHE
We offer pre-developed and characterized advanced co-cultures of human bone marrow endothelial cells (ECs) and mesenchymal stromal cells (MSCs) in the synthetic hydrogels. These co-cultures constitute a model of the (peri)vascular niche which can be used to study angiogenesis and vasculogenesis. It is possible to add blood cancer cells to study the role of the vascular niche on their maintenance and protection from chemotherapies. The endothelial network is organized in three dimensions and displays luminal and basal features.
GLIAL MODELS AND NERVOUS SYSTEM STROMA
We offer pre-developed and characterized cellular models to study the microenvironment of malignant gliomas and inflammatory processes in the nervous system. The ultimate objective is to recreate an artificial culture system comprising neuronal and non-neuronal cells such as glial cells, stromal cells of the nervous system (blood and lymphatic endothelial cells, pericytes, meningeal fibroblasts) and last but not least immune cells. We currently provide robust and well characterized human and non-human glial models of the central and peripheral nervous system. These can be further developed towards co-cultures incorporating malignant glioma cells and stromal components.
PANCREATIC AND PULMONARY TUMOR STROMA
We offer pre-developed and characterized pulmonary and pancreatic tumor stromal models made of patient-derived cancer associated fibroblasts (CAFs) ideal for tumor-stroma interaction studies. The importance of the tumor microenvironment for cancer growth, progression, and metastasis is well recognized. In particular, stromal cells and their extracellular matrix are key factors determining cancer pathophysiology. For example, in lung adenocarcinoma, the stroma component of the cancer determines to a great extent the clinical manifestation of the disease and bears significant prognostic information. CAFs in the stroma can modify cancer epithelial cell phenotype by direct cell-cell contacts, the secretion of soluble factors, or the modification of the extracellular matrix. Such crosstalk between CAF and epithelial cancer cells has been implicated in the development of therapy resistance. It is important to include CAFs and other stromal features in the discovery and safety assays.