Literature DB >> 32399776

In Vitro Modeling of the Tumor Microenvironment in Tumor Organoids.

Mahesh Devarasetty1, Steven D Forsythe1, Ethan Shelkey1, Shay Soker2.   

Abstract

BACKGROUND: The tumor microenvironment (TME) represents the many components occupying the space within and surrounding a tumor, including cells, signaling factors, extracellular matrix, and vasculature. Each component has the potential to assume many forms and functions which in turn contribute to the overall state of the TME, and further contribute to the progression and disposition of the tumor itself. The sum of these components can drive a tumor towards progression, keep a migratory tumor at bay, or even control chemotherapeutic response. The wide potential for interaction that the TME is an integral part of a tumor's ecosystem, and it is imperative to include it when studying and modeling cancer in vitro. Fortunately, the development of tissue engineering and biofabrication technologies and methodologies have allowed widespread inclusion of TME-based factors into in vitro tissue-equivalent models.
METHODS: In this review, we compiled contemporary literature sources to provide an overview of the field of TME models, ranging from simple to complex.
RESULTS: We have identified important components of the TME, how they can be included in in vitro study, and cover examples across a range of cancer types.
CONCLUSION: Our goal with this text is to provide a foundation for prospective research into the TME.

Entities:  

Keywords:  Cancer; Microenvironment; Organoids; Preclinical models

Year:  2020        PMID: 32399776      PMCID: PMC7710785          DOI: 10.1007/s13770-020-00258-4

Source DB:  PubMed          Journal:  Tissue Eng Regen Med        ISSN: 1738-2696            Impact factor:   4.169


  124 in total

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Review 4.  The Tumor Microenvironment Innately Modulates Cancer Progression.

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Journal:  Cancer Res       Date:  2019-07-26       Impact factor: 12.701

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Journal:  Cancer Res       Date:  2008-04-01       Impact factor: 12.701

Review 7.  Hypoxia-adenosinergic immunosuppression: tumor protection by T regulatory cells and cancerous tissue hypoxia.

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Journal:  NPJ Breast Cancer       Date:  2017-03-02

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  9 in total

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