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Updated: Jul 15, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
ErbB-4 may control behavior of prostate cancer cells and serve as a target for molecular therapy
Rami Ben-Yosef1, Alex Starr, Victoria Karaush
1Department of Oncology, Tel-Aviv Sourasky Medical Center, Sackler Faculty of Medicine, Tel-Aviv University, Tel Aviv, Israel. ramiby@post.tau.ac.il
Purpose:
To assess ErbB-4 expression in advanced human prostate cancer (PC) cell lines, the role of ErbB-4 in motility, migration, and proliferative/tumorigenic potential of PC cells, and efficacy of anti-ErbB-4 monoclonal antibody (Mab) treatment on PC cells in vitro and tumor growth in vivo.
Materials And Methods:
Established advanced human PC cell lines (PC-3, Cl-1, and Du-145) were evaluated for ErbB-4 expression. Several Cl-1 cell line clones expressing various levels of ErbB-4 were isolated, their motility, migration capacity, and in vitro proliferation as well as survival following Mab treatment were evaluated. Tumorigenicity and proliferation capacity of these clones in vivo and efficacy of Mab treatment on tumor growth were estimated by measurements of subcutaneous tumors developed in nude mice.
Results:
PC cell lines studied express ErbB-4. Both PC-3 and Du-145 cell lines express high ErbB-4 levels; only 50% of Cl-1 cells express ErbB-4 with large heterogeneity. Cl-1 sub-clones highly expressing ErbB-4 showed increased cell motility, migration, and proliferation rate in vitro and enhanced growth in vivo, compared to clones with low ErbB-4 expression. Mab treatment inhibited the growth of cells expressing high but not low ErbB-4 levels in vitro and decreased the growth of subcutaneous tumors in nude mice generated by ErbB-4 highly expressing cells.
Conclusions:
High expression of ErbB-4 in prostate cancer Cl-1 cell clones correlated with high proliferative and migration capacity and high tumorigenic potential. The inhibitory effect of Mab on cell proliferation and on subcutaneous tumor growth suggests ErbB-4's potential as a target for molecular anticancer therapy.
Insights
High ErbB-4 expression in prostate cancer cells drives proliferation and migration. An anti-ErbB-4 monoclonal antibody (Mab) effectively inhibited cancer cell growth and tumor development in vivo.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Prostate cancer (PC) remains a significant health concern, necessitating novel therapeutic targets.
- ErbB-4, a receptor tyrosine kinase, has been implicated in various cancers, but its role in advanced PC requires further elucidation.
Purpose of the Study:
- To investigate ErbB-4 expression in advanced human prostate cancer cell lines.
- To determine the role of ErbB-4 in PC cell motility, migration, and tumorigenic potential.
- To evaluate the efficacy of an anti-ErbB-4 monoclonal antibody (Mab) against PC cells in vitro and in vivo.
Main Methods:
- ErbB-4 expression was assessed in PC-3, Cl-1, and Du-145 cell lines.
- Cl-1 sub-clones with varying ErbB-4 levels were generated and analyzed for proliferation, migration, and survival after Mab treatment.
- Tumorigenicity and Mab efficacy were evaluated in vivo using subcutaneous tumors in nude mice.
Main Results:
- All studied PC cell lines expressed ErbB-4, with PC-3 and Du-145 showing high levels and Cl-1 exhibiting heterogeneity.
- Cl-1 sub-clones with high ErbB-4 expression demonstrated increased motility, migration, and proliferation in vitro, and enhanced tumor growth in vivo.
- Mab treatment inhibited the proliferation of high-ErbB-4 expressing cells in vitro and reduced tumor growth in vivo.
Conclusions:
- High ErbB-4 expression in prostate cancer cells correlates with increased proliferative, migratory, and tumorigenic potential.
- The anti-ErbB-4 Mab demonstrated significant inhibitory effects on PC cell proliferation and tumor growth.
- ErbB-4 represents a promising therapeutic target for advanced prostate cancer treatment.
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