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Molecular and Pharmacological Bladder Cancer Therapy Screening: Discovery of Clofarabine as a Highly Active Compound
Iris E Ertl1, Ursula Lemberger1, Dafina Ilijazi1
1Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Background:
The heterogeneity of bladder cancers (BCs) is a major challenge for the development of novel therapies. However, given the high rates of recurrence and/or treatment failure, the identification of effective therapeutic strategies is an urgent clinical need.
Objective:
We aimed to establish a model system for drug identification/repurposing in order to identify novel therapies for the treatment of BC.
Design, Setting, And Participants:
A collection of commercially available BC cell lines (n = 32) was comprehensively characterized. A panel of 23 cell lines, representing a broad spectrum of BC, was selected to perform a high-throughput drug screen.
Outcome Measurements And Statistical Analysis:
Positive hits were defined as compounds giving >50% inhibition in at least one BC cell line.
Results And Limitations:
Amongst >1700 tested chemical compounds, a total of 471 substances exhibited antineoplastic effects. Clofarabine, an antimetabolite drug used as third-line treatment for childhood acute lymphoblastic leukaemia, was amongst the limited number of drugs with inhibitory effects on cell lines of all intrinsic subtypes. We, thus, reassessed the substance and confirmed its inhibitory effects on commercially available cell lines and patient-derived cell cultures representing various disease stages, intrinsic subtypes, and histologic variants. To verify these effects in vivo, a patient-derived cell xenograft model for urothelial carcinoma (UC) was used. Well-tolerated doses of clofarabine induced complete remission in all treated animals (n = 12) suffering from both early- and late-stage disease. We further took advantage of another patient-derived cell xenograft model originating from the rare disease entity sarcomatoid carcinoma (SaC). Similarly to UC xenograft mice, clofarabine induced subcomplete to complete tumour remissions in all treated animals (n = 8).
Conclusions:
The potent effects of clofarabine in vitro and in vivo suggest that our findings may be of high clinical relevance. Clinical trials are needed to assess the value of clofarabine in improving BC patient care.
Patient Summary:
We used commercially available cell lines for the identification of novel drugs for the treatment of bladder cancer. We confirmed the effects of one of these drugs, clofarabine, in patient-derived cell lines and two different mouse models, thereby demonstrating a potential clinical relevance of this substance in bladder cancer treatment.
Insights
Clofarabine shows potent anti-cancer effects in bladder cancer models. This antimetabolite drug induced complete remission in preclinical studies, suggesting its potential for treating bladder cancer (BC).
Area of Science:
- Oncology
- Pharmacology
- Cancer Biology
Background:
- Bladder cancer (BC) heterogeneity poses challenges for novel therapy development.
- High rates of recurrence and treatment failure necessitate urgent identification of effective therapeutic strategies for BC.
Purpose of the Study:
- To establish a drug identification and repurposing model system for novel bladder cancer therapies.
- To screen a broad spectrum of bladder cancer cell lines for potential anti-cancer compounds.
Main Methods:
- Comprehensive characterization of 32 commercially available bladder cancer cell lines.
- High-throughput drug screening of 23 selected cell lines against over 1700 chemical compounds.
- In vitro and in vivo validation using patient-derived cell lines and xenograft models (urothelial carcinoma and sarcomatoid carcinoma).
Main Results:
- 471 out of 1700+ compounds exhibited antineoplastic effects.
- Clofarabine demonstrated significant inhibitory effects across all intrinsic bladder cancer subtypes.
- In vivo studies showed complete remission in urothelial carcinoma and subcomplete to complete remission in sarcomatoid carcinoma xenograft models with well-tolerated doses of clofarabine.
Conclusions:
- Clofarabine exhibits potent in vitro and in vivo anti-cancer activity against bladder cancer.
- These findings suggest high clinical relevance for clofarabine in bladder cancer treatment.
- Further clinical trials are warranted to evaluate clofarabine for improving bladder cancer patient care.
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