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Open AccessJournal ArticleDOI

Three-Dimensional in Vitro Cell Culture Models in Drug Discovery and Drug Repositioning.

TLDR
Common approaches to 3D culture are reviewed, the significance of 3D cultures in drug resistance and drug repositioning is discussed and some of the challenges of applying 3D cell cultures to high-throughput drug discovery are addressed.
Abstract
Drug development is a lengthy and costly process that proceeds through several stages from target identification to lead discovery and optimization, preclinical validation and clinical trials culminating in approval for clinical use. An important step in this process is high-throughput screening (HTS) of small compound libraries for lead identification. Currently, the majority of cell-based HTS is being carried out on cultured cells propagated in two-dimensions (2D) on plastic surfaces optimized for tissue culture. At the same time, compelling evidence suggests that cells cultured in these non-physiological conditions are not representative of cells residing in the complex microenvironment of a tissue. This discrepancy is thought to be a significant contributor to the high failure rate in drug discovery, where only a low percentage of drugs investigated ever make it through the gamut of testing and approval to the market. Thus, three-dimensional (3D) cell culture technologies that more closely resemble in vivo cell environments are now being pursued with intensity as they are expected to accommodate better precision in drug discovery. Here we will review common approaches to 3D culture, discuss the significance of 3D cultures in drug resistance and drug repositioning and address some of the challenges of applying 3D cell cultures to high-throughput drug discovery.

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Journal ArticleDOI

Is It Time to Start Transitioning From 2D to 3D Cell Culture

TL;DR: 3D cellculture has the potential to provide alternative ways to study organ behavior via the use of organoids and is expected to eventually bridge the gap between 2D cell culture and animal models.
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3D tumor spheroids as in vitro models to mimic in vivo human solid tumors resistance to therapeutic drugs.

TL;DR: In this review, an overview of the drug resistance mechanisms observed in 3D tumor spheroids is provided, and examples of the therapeutic approaches that have been developed to surpass theDrug resistance mechanisms exhibited by sp heroids are described.
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3D Extracellular Matrix Mimics: Fundamental Concepts and Role of Materials Chemistry to Influence Stem Cell Fate

TL;DR: This review will present the fundamentals of ECM, cover the chemical and structural features of the scaffolds used to generate ECM mimics, discuss the nature of the signaling biomolecules required and exploited to generate bioresponsive cell microenvironments able to induce a specific cell fate, and highlights the syn-thetic strategies involved to create functional 3D ECm mimics.
Journal ArticleDOI

Spheroid Culture System Methods and Applications for Mesenchymal Stem Cells.

TL;DR: Attempts are being made to apply the spheroid culture system to the study of drug delivery platforms and co-cultures, and to regulate differentiation and pluripotency, to overcome the limitations of traditional monolayer cell culture.
Journal ArticleDOI

3D In Vitro Model (R)evolution: Unveiling Tumor–Stroma Interactions

TL;DR: An overview of state-of-the-art 3D models for studying tumor-stroma interactions, with a focus on understanding why the TME is a key target in cancer therapy.
References
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Journal ArticleDOI

Taking Cell-Matrix Adhesions to the Third Dimension

TL;DR: These distinctive in vivo 3D-matrix adhesions differ in structure, localization, and function from classically described in vitro adhesion, and as such they may be more biologically relevant to living organisms.
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