Abstract

The potential of tumor three-dimensional (3D) in vitro models for the validation of existing or novel anti-cancer therapies has been largely recognized. During the last decade, diverse in vitro 3D cell systems have been proposed as a bridging link between two-dimensional (2D) cell cultures and in vivo animal models, both considered gold standards in pre-clinical settings. The latest awareness about the power of tailored therapies and cell-based therapies in eradicating tumor cells raises the need for versatile 3D cell culture systems through which we might rapidly understand the specificity of promising anti-cancer approaches. Yet, a faithful reproduction of the complex tumor microenvironment is demanding as it implies a suitable organization of several cell types and extracellular matrix components. The proposed 3D tumor models discussed here are expected to offer the required structural complexity while also assuring cost-effectiveness during pre-selection of the most promising therapies. As neuroblastoma is an extremely heterogenous extracranial solid tumor, translation from 2D cultures into innovative 3D in vitro systems is particularly challenging. In recent years, the number of 3D in vitro models mimicking native neuroblastoma tumors has been rapidly increasing. However, in vitro platforms that efficiently sustain patient-derived tumor cell growth, thus allowing comprehensive drug discovery studies on tailored therapies, are still lacking. In this review, the latest neuroblastoma 3D in vitro models are presented and their applicability for a more accurate prediction of therapy outcomes is discussed.

Highlights

  • The turn of the 20th century was crucial for the development of the basic principles for in vitro cell growth enabled substantial biological discoveries

  • The major obstacle to a straightforward translation of in vitro biological process analyzed in 2D conditions into an in vivo response is the lack of multicellular systems that are in direct contact with the cellextracellular matrix (ECM) components [5]

  • Multicellular Tumor Spheroids (MCTSs) obtained by the aggregation of neuroblastoma cell lines represent an attractive tool to reproduce in vitro the in vivo characteristics of tumor cells with respect to the production of EXTRACELLULAR MATRIX (ECM), cell–cell interactions, growth kinetics, cellular heterogeneity, signal pathway activity, and gene expression [13, 25]

Read more

Summary

Introduction

The turn of the 20th century was crucial for the development of the basic principles for in vitro cell growth enabled substantial biological discoveries. MCTSs obtained by the aggregation of neuroblastoma cell lines represent an attractive tool to reproduce in vitro the in vivo characteristics of tumor cells with respect to the production of ECM, cell–cell interactions, growth kinetics, cellular heterogeneity, signal pathway activity, and gene expression [13, 25].

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call