Exploring therapeutic strategies for androgen-independent prostate cancer using a magnetic coculture platform

Prostate cancer stands as the most diagnosed cancer in males and remains one of the leading causes of death among men in the United States. The progression of prostate cancer to a life-threatening state occurs upon metastasis, typically spreading to vital organs such as the liver, lungs, bones, and...

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Main Authors: Anjani Chavali, Giles Fitzwilliams, Adam Germain, Sandra Khuon, Young-tae Kim
Format: Article
Language:English
Published: Elsevier 2025-06-01
Series:Biomedical Engineering Advances
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Online Access:http://www.sciencedirect.com/science/article/pii/S2667099225000015
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author Anjani Chavali
Giles Fitzwilliams
Adam Germain
Sandra Khuon
Young-tae Kim
author_facet Anjani Chavali
Giles Fitzwilliams
Adam Germain
Sandra Khuon
Young-tae Kim
author_sort Anjani Chavali
collection DOAJ
description Prostate cancer stands as the most diagnosed cancer in males and remains one of the leading causes of death among men in the United States. The progression of prostate cancer to a life-threatening state occurs upon metastasis, typically spreading to vital organs such as the liver, lungs, bones, and lymph nodes, where it sustains growth even in the absence of androgens. In this study, we employed a magnetic coculture device to investigate the interactions between androgen-independent prostate cancer (PC3) cells and healthy normal fibroblasts, aiming to discern their dynamics. Subsequently, the coculture was exposed to varying dosages of Fenbendazole to assess its efficacy differentially on healthy fibroblasts compared to androgen-independent prostate cells. Employing this straightforward coculture method, we observed significant growth, motility, and cluster formation of prostate cancer cells upon direct contact with surrounding fibroblasts. The impact of Fenbendazole was evident in its capacity to markedly diminish the growth and metastasis of prostate cancer cells relative to surrounding fibroblasts. Notably, our findings revealed that a dosage of 2.5 µM Fenbendazole significantly eradicated PC3 cells with minimal damage to surrounding fibroblasts, thus indicating its potential for prostate cancer treatment in-vivo models.
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spelling doaj-art-a7598b98ebcd473d8b1aff53190bf2372025-01-26T05:05:17ZengElsevierBiomedical Engineering Advances2667-09922025-06-019100144Exploring therapeutic strategies for androgen-independent prostate cancer using a magnetic coculture platformAnjani Chavali0Giles Fitzwilliams1Adam Germain2Sandra Khuon3Young-tae Kim4Department of Bioengineering, University of Texas at Arlington, Arlington, TX, USADepartment of Bioengineering, University of Texas at Arlington, Arlington, TX, USA; Corresponding authors at: Associate Professor, Department of Bioengineering, University of Texas at Arlington, TX USA.Department of Bioengineering, University of Texas at Arlington, Arlington, TX, USADepartment of Nursing, University of Texas at Arlington, Arlington, TX, USADepartment of Bioengineering, University of Texas at Arlington, Arlington, TX, USA; Department of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA; Corresponding authors at: Associate Professor, Department of Bioengineering, University of Texas at Arlington, TX USA.Prostate cancer stands as the most diagnosed cancer in males and remains one of the leading causes of death among men in the United States. The progression of prostate cancer to a life-threatening state occurs upon metastasis, typically spreading to vital organs such as the liver, lungs, bones, and lymph nodes, where it sustains growth even in the absence of androgens. In this study, we employed a magnetic coculture device to investigate the interactions between androgen-independent prostate cancer (PC3) cells and healthy normal fibroblasts, aiming to discern their dynamics. Subsequently, the coculture was exposed to varying dosages of Fenbendazole to assess its efficacy differentially on healthy fibroblasts compared to androgen-independent prostate cells. Employing this straightforward coculture method, we observed significant growth, motility, and cluster formation of prostate cancer cells upon direct contact with surrounding fibroblasts. The impact of Fenbendazole was evident in its capacity to markedly diminish the growth and metastasis of prostate cancer cells relative to surrounding fibroblasts. Notably, our findings revealed that a dosage of 2.5 µM Fenbendazole significantly eradicated PC3 cells with minimal damage to surrounding fibroblasts, thus indicating its potential for prostate cancer treatment in-vivo models.http://www.sciencedirect.com/science/article/pii/S2667099225000015Magnetic coculture platformCancer-normal healthy cell interfaceMetastasisAndrogen-independent prostate cancerAnd drug discovery
spellingShingle Anjani Chavali
Giles Fitzwilliams
Adam Germain
Sandra Khuon
Young-tae Kim
Exploring therapeutic strategies for androgen-independent prostate cancer using a magnetic coculture platform
Biomedical Engineering Advances
Magnetic coculture platform
Cancer-normal healthy cell interface
Metastasis
Androgen-independent prostate cancer
And drug discovery
title Exploring therapeutic strategies for androgen-independent prostate cancer using a magnetic coculture platform
title_full Exploring therapeutic strategies for androgen-independent prostate cancer using a magnetic coculture platform
title_fullStr Exploring therapeutic strategies for androgen-independent prostate cancer using a magnetic coculture platform
title_full_unstemmed Exploring therapeutic strategies for androgen-independent prostate cancer using a magnetic coculture platform
title_short Exploring therapeutic strategies for androgen-independent prostate cancer using a magnetic coculture platform
title_sort exploring therapeutic strategies for androgen independent prostate cancer using a magnetic coculture platform
topic Magnetic coculture platform
Cancer-normal healthy cell interface
Metastasis
Androgen-independent prostate cancer
And drug discovery
url http://www.sciencedirect.com/science/article/pii/S2667099225000015
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AT adamgermain exploringtherapeuticstrategiesforandrogenindependentprostatecancerusingamagneticcocultureplatform
AT sandrakhuon exploringtherapeuticstrategiesforandrogenindependentprostatecancerusingamagneticcocultureplatform
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