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Updated: Mar 19, 2026

Induction of Invasive Transitional Cell Bladder Carcinoma in Immune Intact Human MUC1 Transgenic Mice: A Model for Immunotherapy Development
Published on: October 30, 2013
Identification of targeted therapy for an aggressive subgroup of muscle-invasive bladder cancers
Thierry Lebret1, Yann Neuzillet1, Nadine Houede2
1Service d'Urologie; Hôpital Foch; Suresnes, France; Université de Versailles; Saint-Quentin-en-Yvelines; Faculté de Médecine Paris; Ile-de-France Ouest; Guyancourt, France.
Abstract:
Rebouissou et al. recently provided preclinical evidence that a subset of patients with muscle-invasive bladder cancer might benefit from anti-epidermal growth factor receptor (EGFR) therapy and reported diagnostic tools for identifying these patients in the clinical setting. This work also identified relevant experimental models that may be useful for future basic and clinical research on this subgroup of tumors.
Insights
Certain muscle-invasive bladder cancer patients may benefit from anti-epidermal growth factor receptor (EGFR) therapy. Researchers identified diagnostic tools and models for this patient subset in preclinical studies.
Area of Science:
- Oncology
- Cancer Research
- Molecular Biology
Background:
- Muscle-invasive bladder cancer (MIBC) is a significant clinical challenge.
- Identifying predictive biomarkers for targeted therapies in MIBC is crucial.
- Epidermal growth factor receptor (EGFR) is a potential therapeutic target in various cancers.
Purpose of the Study:
- To investigate the potential benefit of anti-epidermal growth factor receptor (EGFR) therapy in a subset of muscle-invasive bladder cancer (MIBC) patients.
- To identify diagnostic tools for selecting patients who may respond to anti-EGFR therapy.
- To establish relevant preclinical models for future research on this MIBC subgroup.
Main Methods:
- Preclinical studies were conducted to evaluate the efficacy of anti-EGFR therapy.
- Diagnostic strategies were developed and assessed for patient stratification.
- Experimental models representing specific MIBC subtypes were established.
Main Results:
- Preclinical evidence suggests that a subset of MIBC patients may benefit from anti-EGFR therapy.
- Diagnostic tools capable of identifying these responsive patients were reported.
- Suitable experimental models were identified for further investigation.
Conclusions:
- Targeted anti-EGFR therapy holds promise for a specific group of MIBC patients.
- The developed diagnostic tools can aid in clinical patient selection.
- The identified experimental models will facilitate future research into this MIBC subtype.
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