Related Experiment Video
Updated: Jul 26, 2025

High-throughput Screening for Chemical Modulators of Post-transcriptionally Regulated Genes
Published on: March 3, 2015
Translational screening platform to evaluate chemotherapy in combination with focal therapy for retinoblastoma
Irina L Sinenko1,2, Fabien Kuttler3, Valentin Simeonov4
1Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Abstract:
Retinoblastoma is the most common pediatric eye cancer. It is currently treated with a limited number of drugs, adapted from other pediatric cancer treatments. Drug toxicity and relapse of the disease warrant new therapeutic strategies for these young patients. In this study, we developed a robust tumoroid-based platform to test chemotherapeutic agents in combination with focal therapy (thermotherapy) - a treatment option widely used in clinical practice - in accordance with clinically relevant trial protocols. The model consists of matrix-embedded tumoroids that retain retinoblastoma features and respond to repeated chemotherapeutic drug exposure similarly to advanced clinical cases. Moreover, the screening platform includes a diode laser (810 nm, 0.3 W) to selectively heat the tumoroids, combined with an on-line system to monitor the intratumoral and surrounding temperatures. This allows the reproduction of the clinical settings of thermotherapy and combined chemothermotherapy treatments. When testing the two main drugs currently used in clinics to treat retinoblastoma in our model, we observed results similar to those clinically obtained, validating the utility of the model. This screening platform is the first system to accurately reproduce clinically relevant treatment methods and should lead to the identification of more efficient drugs to treat retinoblastoma.
Insights
Researchers developed a new tumoroid model to test retinoblastoma (RB) treatments. This platform accurately mimics clinical conditions, paving the way for discovering more effective chemotherapy and thermotherapy combinations for pediatric eye cancer.
Area of Science:
- Oncology
- Ophthalmology
- Biomedical Engineering
Background:
- Retinoblastoma (RB) is the most frequent pediatric eye cancer.
- Current RB treatments face challenges due to drug toxicity and disease relapse.
- Novel therapeutic strategies are crucial for improving outcomes in young patients.
Purpose of the Study:
- To develop a robust tumoroid-based platform for screening retinoblastoma (RB) chemotherapeutic agents.
- To integrate focal therapy (thermotherapy) into the screening platform to mimic clinical treatment protocols.
- To validate the platform's ability to reproduce clinically relevant treatment responses.
Main Methods:
- Developed matrix-embedded tumoroids that preserve RB characteristics and drug response.
- Incorporated a diode laser (810 nm, 0.3 W) for selective tumoroid heating (thermotherapy).
- Implemented an online system for real-time monitoring of intratumoral and surrounding temperatures.
Main Results:
- The tumoroid model demonstrated responses to chemotherapy consistent with advanced clinical cases.
- The platform successfully reproduced clinical settings for thermotherapy and combined chemothermotherapy.
- Testing known RB drugs yielded results comparable to those observed in clinical practice, validating the model.
Conclusions:
- The developed tumoroid-based screening platform is the first to accurately replicate clinically relevant retinoblastoma treatment methods.
- This novel system holds significant potential for identifying more effective therapeutic agents and drug combinations for retinoblastoma.
- The platform offers a promising avenue for advancing treatment strategies and improving outcomes for pediatric eye cancer patients.
More Related Videos
05:29A Rapid Screening Workflow to Identify Potential Combination Therapy for GBM using Patient-Derived Glioma Stem Cells
Published on: March 28, 2021
10:13A Multiplexed Luciferase-based Screening Platform for Interrogating Cancer-associated Signal Transduction in Cultured Cells
Published on: July 3, 2013