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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
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Amorphous calcium phosphate-coated surfaces as a model for bone microenvironment in prostate cancer
Rebeca San Martin1, Prijoyit Das2, Tianchun Xue2
1Department of Biochemistry & Cellular and Molecular Biology, University of Tennessee, 309 Ken and Blaire Mossman Bldg. 1311 Cumberland Ave, Knoxville, TN, 37996, USA.
Heliyon
|February 11, 2025
Summary
A novel in-vitro system using amorphous calcium phosphate (ACP) enhances prostate cancer cell adhesion and proliferation, mimicking bone metastasis. This cost-effective model aids in studying cancer progression and developing pre-clinical treatments.
Area of Science:
- Oncology
- Biomaterials Science
- Cell Biology
Background:
- Bone metastasis is a significant challenge in treating prostate and other solid tumors.
- In-vitro modeling of the bone microenvironment requires understanding cell-cell interactions, extracellular matrix, and high calcium levels.
Purpose of the Study:
- To develop a fast, cost-effective in-vitro system for modeling bone metastasis.
- To investigate the effect of amorphous calcium phosphate (ACP) on cancer cell behavior.
Main Methods:
- Coating non-adhesive cell culture vessels with amorphous calcium phosphate (ACP) as a bone matrix surrogate.
- Developing protocols for cell culture, nucleic acid, and protein collection in high-calcium environments.
Main Results:
- Prostate epithelial cell lines exhibited increased adhesion and proliferation on ACP surfaces.
- Cancer cells cultured on ACP showed independence from androgen starvation.
- Gene expression changes in adenocarcinoma cells on ACP surfaces were relevant to prostate cancer progression.
Conclusions:
- Biologically relevant in-vitro systems are crucial for accurately modeling cancer progression.
- Calcium availability and signaling are critical for cancer cell survival in bone metastasis.
- The ACP system provides a valuable tool for pre-clinical modeling of bone metastasis.
Keywords:
Amorphous calcium phosphateAndrogen resistanceBone metastasisCell culture modelingGene expressionProstate cancer
