Evidence map›Paper›PMID 30393802›Full record

ArticleLab on a chip2018

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

Venktesh S Shirure, Ye Bi, Matthew B Curtis, Andrew Lezia, Madeleine M Goedegebuure, S Peter Goedegebuure, Rebecca Aft, Ryan C Fields, Steven C George

Open access · greenAbstract read
In one paragraph

Article in Lab on a chip, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 176 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
176citing papers in PubMed, 2 pooled it
11.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

176 citing papers in PubMed, 2 syntheses or guidelines pooled it, 281 citations in OpenAlex.

  1. Pooled it
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  13. Progress and challenges in the development of advanced pancreatic cancer organoids.Journal of experimental & clinical cancer research : CR · 2026
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  16. Tumor organoid-immune cell co-culture systems for precision oncology.Frontiers in cell and developmental biology · 2026
    Review
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116 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Venktesh S ShirureDepartment of Biomedical Engineering, University of California, Davis, CA 95616, USA. scgeorge@ucdavis.edu.ORCID 0000-0002-4430-2612
Ye BiDepartment of Surgery, Washington University School of Medicine, St. Louis, USA.
Matthew B CurtisDepartment of Biomedical Engineering, University of California, Davis, CA 95616, USA. scgeorge@ucdavis.edu.
Andrew LeziaDepartment of Biomedical Engineering, Washington University in St. Louis, USA.ORCID 0000-0001-8068-8834
Madeleine M GoedegebuureWashington University School of Engineering and Applied Science, St. Louis, MO 63130, USA.
S Peter GoedegebuureDepartment of Surgery, Washington University School of Medicine, St. Louis, USA and Siteman Cancer Center at the Washington University School of Medicine, St. Louis, USA.
Rebecca AftDepartment of Surgery, Washington University School of Medicine, St. Louis, USA and Siteman Cancer Center at the Washington University School of Medicine, St. Louis, USA and Johan Cochran Veterans Administration Hospital, St. Louis, MO 63110, USA.
Ryan C FieldsDepartment of Surgery, Washington University School of Medicine, St. Louis, USA and Siteman Cancer Center at the Washington University School of Medicine, St. Louis, USA.
Steven C GeorgeDepartment of Biomedical Engineering, University of California, Davis, CA 95616, USA. scgeorge@ucdavis.edu.
Washington University in St. Louis · USUniversity of California System · USUniversity of Washington · US

Funding

Linking DDR2 expression, the cancer-associated fibroblast, and angiogenesis in the tumor microenvironmentUH3TR000481 · NCATS · WASHINGTON UNIVERSITY · PI GEORGE, STEVEN CARL · 2014 to 2016
$2.8M
A 3-D In Vitro Platform of Tumor Metastasis (PQ24)R01CA170879 · NCI · WASHINGTON UNIVERSITY · PI GEORGE, STEVEN CARL · 2012 to 2015
$1.3M
Advancing Cancer Biology, Diagnostics and Therapeutics Outside of the Patient: Creation of a Novel, Autologous, Ex Vivo, Vascularized Model of the Tumor MicroenvironmentR21CA223836 · NCI · WASHINGTON UNIVERSITY · PI FIELDS, RYAN C · 2018 to 2019
$601k
Center for Clinical and Translational ScienceKL2TR000048 · NCATS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI AZAR, DIMITRI T, MERMELSTEIN, ROBIN J. · 2012 to 2014
$559k
NCATS NIH HHS KL2 TR000048NCATS NIH HHS UH3 TR000481NCI NIH HHS R01 CA170879NCI NIH HHS R21 CA223836
6 · The paper itself

Abstract

Most cancer treatment strategies target cell proliferation, angiogenesis, migration, and intravasation of tumor cells in an attempt to limit tumor growth and metastasis. An in vitro platform to assess tumor progression and drug sensitivity could provide avenues to enhance our understanding of tumor metastasis as well as precision medicine. We present a microfluidic platform that mimics biological mass transport near the arterial end of a capillary in the tumor microenvironment. A central feature is a quiescent perfused 3D microvascular network created prior to loading tumor cells or patient-derived tumor organoids in an adjacent compartment. The physiological delivery of nutrients and/or drugs to the tumor then occurs through the vascular network. We demonstrate the culture, growth, and treatment of tumor cell lines and patient-derived breast cancer organoids. The platform provides the opportunity to simultaneously and dynamically observe hallmark features of tumor progression including cell proliferation, angiogenesis, cell migration, and tumor cell intravasation. Additionally, primary breast tumor organoids are viable in the device for several weeks and induce robust sprouting angiogenesis. Finally, we demonstrate the feasibility of our platform for drug discovery and personalized medicine by analyzing the response to chemo- and anti-angiogenic therapy. Precision medicine-based cancer treatments can only be realized if individual tumors can be rapidly assessed for therapeutic sensitivity in a clinically relevant timeframe (⪅14 days). Our platform indicates that this goal can be achieved and provides compelling opportunities to advance precision medicine for cancer.

Indexed as

Lab-On-A-Chip DevicesCell Line, TumorCell ProliferationDrug Screening Assays, AntitumorEquipment DesignHumansMicrovesselsNeoplasm InvasivenessOrganoidsTumor Microenvironment

Identifiers

PMID30393802
PMCPMC10644986
OpenAlexW2900098081

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.