Literature DB >> 26688098

Recapitulation of complex transport and action of drugs at the tumor microenvironment using tumor-microenvironment-on-chip.

Bumsoo Han1, Chunjing Qu2, Kinam Park3, Stephen F Konieczny2, Murray Korc4.   

Abstract

Targeted delivery aims to selectively distribute drugs to targeted tumor tissues but not to healthy tissues. This can address many clinical challenges by maximizing the efficacy but minimizing the toxicity of anti-cancer drugs. However, a complex tumor microenvironment poses various barriers hindering the transport of drugs and drug delivery systems. New tumor models that allow for the systematic study of these complex environments are highly desired to provide reliable test beds to develop drug delivery systems for targeted delivery. Recently, research efforts have yielded new in vitro tumor models, the so called tumor-microenvironment-on-chip, that recapitulate certain characteristics of the tumor microenvironment. These new models show benefits over other conventional tumor models, and have the potential to accelerate drug discovery and enable precision medicine. However, further research is warranted to overcome their limitations and to properly interpret the data obtained from these models. In this article, key features of the in vivo tumor microenvironment that are relevant to drug transport processes for targeted delivery were discussed, and the current status and challenges for developing in vitro transport model systems were reviewed.
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Drug transport; Microfluidics; Nanoparticles; Stromal tissue; Targeted delivery

Mesh:

Substances:

Year:  2015        PMID: 26688098      PMCID: PMC4902790          DOI: 10.1016/j.canlet.2015.12.003

Source DB:  PubMed          Journal:  Cancer Lett        ISSN: 0304-3835            Impact factor:   8.679


  144 in total

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Review 3.  Lymphatic and interstitial flow in the tumour microenvironment: linking mechanobiology with immunity.

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5.  Lowering of tumoral interstitial fluid pressure by prostaglandin E(1) is paralleled by an increased uptake of (51)Cr-EDTA.

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Journal:  Int J Cancer       Date:  2000-06-01       Impact factor: 7.396

6.  The penetration of anticancer drugs through tumor tissue as a function of cellular adhesion and packing density of tumor cells.

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8.  Pancreatic cancer stroma: friend or foe?

Authors:  Jesse Gore; Murray Korc
Journal:  Cancer Cell       Date:  2014-06-16       Impact factor: 31.743

9.  An agarose-based microfluidic platform with a gradient buffer for 3D chemotaxis studies.

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  10 in total

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4.  Characterization of Cell-Type-Specific Drug Transport and Resistance of Breast Cancers Using Tumor-Microenvironment-on-Chip.

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5.  An engineered pancreatic cancer model with intra-tumoral heterogeneity of driver mutations.

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6.  Dynamic Microenvironment Induces Phenotypic Plasticity of Esophageal Cancer Cells Under Flow.

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Review 7.  Mimicking Tumors: Toward More Predictive In Vitro Models for Peptide- and Protein-Conjugated Drugs.

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8.  3D collagen fibrillar microstructure guides pancreatic cancer cell phenotype and serves as a critical design parameter for phenotypic models of EMT.

Authors:  T J Puls; Xiaohong Tan; Catherine F Whittington; Sherry L Voytik-Harbin
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Review 9.  Ex vivo tumor culture systems for functional drug testing and therapy response prediction.

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  10 in total

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