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3-D Cell Culture System for Studying Invasion and Evaluating Therapeutics in Bladder Cancer
Published on: September 13, 2018
Fluorescent imaging of high-grade bladder cancer using a specific antagonist for chemokine receptor CXCR4
Koji Nishizawa1, Hiroyuki Nishiyama, Shinya Oishi
1Department of Urology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Abstract:
We previously reported that the expression of CXC chemokine receptor-4 (CXCR4) was upregulated in invasive bladder cancers and that the small peptide T140 was a highly sensitive antagonist for CXCR4. In this study, we identified that CXCR4 expression was induced in high-grade superficial bladder tumors, including carcinoma in situ and invasive bladder tumors. To visualize the bladder cancer cells using urinary sediments from the patients and chemically induced mouse bladder cancer model, a novel fluorescent CXCR4 antagonist TY14003 was developed, that is a T140 derivative. TY14003 could label bladder cancer cell lines expressing CXCR4, whereas negative-control fluorescent peptides did not label them. When labeling urinary sediments from patients with invasive bladder cancer, positive-stained cells were identified in all patients with bladder cancer and positive urine cytology but not in controls. Although white blood cells in urine were also labeled with TY14003, they could be easily discriminated from urothelial cells by their shape and size. Finally, intravesical instillation of TY14003 into mouse bladder, using N-butyl-N-(4-hydroxybutyl) nitrosamine (BBN)-induced bladder cancer model, demonstrated that fluorescent signals were detected in the focal areas of bladder of all mice examined at 12 weeks of BBN drinking by confocal microscopy and fluorescent endoscopy. On the contrary, all the normal bladders were found to be negative for TY14003 staining. In conclusion, these results indicate that TY14003 is a promising diagnostic tool to visualize small or flat high-grade superficial bladder cancer.
Insights
A novel fluorescent peptide, TY14003, effectively labels bladder cancer cells by targeting CXC chemokine receptor-4 (CXCR4). This diagnostic tool shows promise for visualizing high-grade superficial bladder tumors in patients and mouse models.
Area of Science:
- Oncology
- Molecular Imaging
- Urology
Background:
- CXC chemokine receptor-4 (CXCR4) is upregulated in invasive bladder cancers.
- CXCR4 expression is induced in high-grade superficial bladder tumors, including carcinoma in situ.
- Previous work identified T140 as a CXCR4 antagonist.
Purpose of the Study:
- To develop a novel fluorescent CXCR4 antagonist for visualizing bladder cancer cells.
- To evaluate the diagnostic potential of TY14003 in patient urinary sediments and a mouse bladder cancer model.
Main Methods:
- Development of TY14003, a fluorescent derivative of T140.
- Labeling of bladder cancer cell lines and patient urinary sediments with TY14003.
- Intravesical instillation of TY14003 in a chemically induced mouse bladder cancer model (BBN).
- Detection of fluorescent signals using confocal microscopy and fluorescent endoscopy.
Main Results:
- TY14003 specifically labeled bladder cancer cell lines expressing CXCR4.
- Positive TY14003 staining was observed in urinary sediments of all bladder cancer patients with positive urine cytology.
- Fluorescent signals were detected in the bladders of mice with induced bladder cancer, but not in normal bladders.
Conclusions:
- TY14003 is a novel fluorescent peptide that can effectively label bladder cancer cells.
- TY14003 demonstrates potential as a diagnostic tool for visualizing high-grade superficial bladder cancer.
- This approach may aid in the early detection of small or flat bladder tumors.
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