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Published on: April 6, 2016
Tumor in 3D: In Vitro Complex Cellular Models to Improve Nanodrugs Cancer Therapy
Soraia Fernandes1, Marco Cassani1, Stefania Pagliari1
1International Clinical Research Center (ICRC) of St Anne’s University Hospital, CZ-65691 Brno, Czech Republic
Abstract:
Nanodrugs represent novel solutions to reshuffle repurposed drugs for cancer therapy. They might offer different therapeutic options by combining targeted drug delivery and imaging in unique platforms. Such nanomaterials are deemed to overcome the limitations of currently available treatments, ultimately improving patients' life quality. However, despite these promises being made for over three decades, the poor clinical translation of nanoparticle- based therapies calls for deeper in vit.. and in vivo investigations. Translational issues arise very early during the development of nanodrugs, where complex and more reliable cell models are often replaced by easily accessible and convenient 2D monocultures. This is particularly true in the field of cancer therapy. In fact, 2D monocultures provide poor information about the real impact of the nanodrugs in a complex living organism, especially given the poor mimicry of the solid Tumors Microenvironment (TME). The dense and complex extracellular matrix (ECM) of solid tumors dramatically restricts nanoparticles efficacy, impairing the successful implementation of nanodrugs in medical applications. Herein, we propose a comprehensive guideline of the 3D cell culture models currently available, including their potential and limitations for the evaluation of nanodrugs activity. Advanced culture techniques, more closely resembling the physiological conditions of the TME, might give a better prediction of the reciprocal interactions between cells and nanoparticles and eventually help reconsider the use of old drugs for new applications.
Insights
Advanced 3D cell culture models offer better insights into nanodrug efficacy for cancer therapy. These models more accurately mimic the tumor microenvironment (TME), improving the translation of nanoparticle-based treatments.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Cancer Research
Background:
- Nanodrugs show promise for cancer therapy by combining drug delivery and imaging.
- However, poor clinical translation is linked to limitations in current preclinical models.
- 2D monocultures inadequately represent the complex tumor microenvironment (TME).
Purpose of the Study:
- To provide a comprehensive guideline on 3D cell culture models for evaluating nanodrugs.
- To highlight the potential and limitations of these advanced models.
- To improve the prediction of nanodrug efficacy in cancer therapy.
Main Methods:
- Review and analysis of available 3D cell culture techniques.
- Comparison of 3D models with traditional 2D monocultures.
- Assessment of 3D models' ability to mimic the TME and extracellular matrix (ECM).
Main Results:
- 3D cell cultures offer superior mimicry of the TME compared to 2D models.
- The complex ECM in 3D models significantly impacts nanoparticle penetration and efficacy.
- Advanced models provide better insights into cell-nanoparticle interactions.
Conclusions:
- 3D cell culture models are crucial for accurate nanodrug evaluation in cancer research.
- These models can enhance the clinical translation of nanoparticle-based therapies.
- Revisiting repurposed drugs with 3D models may unlock new therapeutic applications.

