Literature DB >> 28568605

Vascular beds maintain pancreatic tumour explants for ex vivo drug screening.

Despina Bazou1, Nir Maimon1, Gabriel Gruionu2, Jelena Grahovac1, Giorgio Seano1, Hao Liu1, Conor L Evans3, Lance L Munn1.   

Abstract

Our understanding of cancer progression or response to therapies would benefit from benchtop, tissue-level assays that preserve the biology and anatomy of human tumours ex vivo. We present a methodology for maintaining patient tumour samples ex vivo for the purpose of drug testing in a clinical setting. The harvested tumour biopsy, excised from mice or patients, is integrated into a support tissue that includes stroma and vasculature. This support tissue preserves tumour histoarchitecture and relevant expression profiles, and tumour tissues cultured using this system display different sensitivities to chemotherapeutics compared with tumour explants with no supporting tissue. The methodology is more rapid than patient-derived xenograft models, easy to implement, and amenable to high-throughput assays, making it an attractive tool for in vitro drug screening or for the guidance of patient-specific chemotherapies.
Copyright © 2017 John Wiley & Sons, Ltd.

Entities:  

Keywords:  cancer; chemotherapy; high-throughput assay; pancreatic; tumour explant; vascular bed; vascularization

Mesh:

Year:  2017        PMID: 28568605      PMCID: PMC5711628          DOI: 10.1002/term.2481

Source DB:  PubMed          Journal:  J Tissue Eng Regen Med        ISSN: 1932-6254            Impact factor:   3.963


  12 in total

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10.  Organotypic slice cultures of human glioblastoma reveal different susceptibilities to treatments.

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Journal:  Neuro Oncol       Date:  2013-04-10       Impact factor: 12.300

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