Tumor-on-a-chip platform to investigate progression and drug sensitivity in cell lines and patient-derived organoids-Reference-Cited by-同舟云学术

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Tumor-on-a-chip platform to investigate progression and drug sensitivity in cell lines and patient-derived organoids

Published:2018 Issue:23 Volume:18 Page:3687-3702
ISSN:1473-0197
Container-title:Lab on a Chip
language:en
Short-container-title:Lab Chip

Author:

Shirure Venktesh S.¹²³⁴^ORCID,Bi Ye⁵⁶⁷⁴,Curtis Matthew B.¹²³⁴,Lezia Andrew¹⁸⁴^ORCID,Goedegebuure Madeleine M.⁹⁷⁴,Goedegebuure S. Peter⁵⁶⁷⁴¹⁰,Aft Rebecca⁵⁶⁷⁴¹⁰,Fields Ryan C.⁵⁶⁷⁴¹⁰,George Steven C.¹²³⁴

Affiliation:

1. Department of Biomedical Engineering

2. University of California

3. Davis

4. USA

5. Department of Surgery

6. Washington University School of Medicine

7. St. Louis

8. Washington University in St. Louis

9. Washington University School of Engineering and Applied Science

10. Siteman Cancer Center at the Washington University School of Medicine

Abstract

We created a tumor platform to study cell proliferation, angiogenesis, migration, intravasation, and treatments.

Funder

National Institutes of Health

Publisher

Royal Society of Chemistry (RSC)

Subject

Biomedical Engineering,General Chemistry,Biochemistry,Bioengineering

Link

http://pubs.rsc.org/en/content/articlepdf/2018/LC/C8LC00596F

Reference43 articles.

1. In Vitro Perfused Human Capillary Networks

2. 3D microtumors in vitro supported by perfused vascular networks

3. Low levels of physiological interstitial flow eliminate morphogen gradients and guide angiogenesis

4. Rapid Anastomosis of Endothelial Progenitor Cell–Derived Vessels with Host Vasculature Is Promoted by a High Density of Cotransplanted Fibroblasts

5. Molecular Distinction and Angiogenic Interaction between Embryonic Arteries and Veins Revealed by ephrin-B2 and Its Receptor Eph-B4

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