Evidence map›Paper›PMID 30650355›Full record

ArticleCell reports2019

Modeling Tumor Phenotypes In Vitro with Three-Dimensional Bioprinting.

Ellen M Langer, Brittany L Allen-Petersen, Shelby M King, Nicholas D Kendsersky, Megan A Turnidge, Genevra M Kuziel, Rachelle Riggers, Ravi Samatham, Taylor S Amery, Steven L Jacques and 9 more

Abstract read
In one paragraph

Article in Cell reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

125 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  13. 3D bioprinting innovations: a new frontier in breast cancer research.Medical oncology (Northwood, London, England) · 2025
    Review
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65 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

19 authors.

Ellen M LangerDepartment of Medical and Molecular Genetics, Oregon Health & Science University, Portland, OR 97201, USA.
Brittany L Allen-PetersenDepartment of Medical and Molecular Genetics, Oregon Health & Science University, Portland, OR 97201, USA.
Shelby M KingTissue Applications, Organovo, Inc., San Diego, CA 92121, USA.
Nicholas D KendserskyDepartment of Medical and Molecular Genetics, Oregon Health & Science University, Portland, OR 97201, USA.
Megan A TurnidgeDepartment of Medical and Molecular Genetics, Oregon Health & Science University, Portland, OR 97201, USA.
Genevra M KuzielDepartment of Medical and Molecular Genetics, Oregon Health & Science University, Portland, OR 97201, USA.
Rachelle RiggersDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA.
Ravi SamathamDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA.
Taylor S AmeryDepartment of Medical and Molecular Genetics, Oregon Health & Science University, Portland, OR 97201, USA.
Steven L JacquesDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA.
Brett C SheppardDepartment of Surgery, Oregon Health & Science University, Portland, OR 97239, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97201, USA.
James E KorkolaDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97201, USA.
John L MuschlerDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97201, USA.
Guillaume ThibaultDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA.
Young Hwan ChangDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA.
Joe W GrayDepartment of Biomedical Engineering, Oregon Health & Science University, Portland, OR 97239, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97201, USA; OHSU Center for Spatial Systems Biomedicine, Oregon Health & Science University, Portland, OR 97201, USA.
Sharon C PresnellTissue Applications, Organovo, Inc., San Diego, CA 92121, USA.
Deborah G NguyenTissue Applications, Organovo, Inc., San Diego, CA 92121, USA.
Rosalie C SearsDepartment of Medical and Molecular Genetics, Oregon Health & Science University, Portland, OR 97201, USA; Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97201, USA. Electronic address: searsr@ohsu.edu.

Funding

Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Luiz Eduardo Bertassoni · 1997 to 2026
$60.5M
Understanding the Impact of Microscale and Nanoscale Heterogeneity and ResistanceU54CA209988 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI DEMIR, EMEK, HEISER, LAURA MADELINE · 2017 to 2021
$10.3M
Hydroxylation regulation of c-MycR01CA186241 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Mu-Shui Dai, ROSALIE C SEARS · 2015 to 2026
$4.2M
The Role of post-translational activation of Myc in pancreatic cancerR01CA196228 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI SEARS, ROSALIE C · 2015 to 2019
$2.0M
NCI NIH HHS HHSN261201400024CNCI NIH HHS P30 CA069533NCI NIH HHS R01 CA186241NCI NIH HHS R01 CA196228NCI NIH HHS U54 CA209988
6 · The paper itself

Abstract

The tumor microenvironment plays a critical role in tumor growth, progression, and therapeutic resistance, but interrogating the role of specific tumor-stromal interactions on tumorigenic phenotypes is challenging within in vivo tissues. Here, we tested whether three-dimensional (3D) bioprinting could improve in vitro models by incorporating multiple cell types into scaffold-free tumor tissues with defined architecture. We generated tumor tissues from distinct subtypes of breast or pancreatic cancer in relevant microenvironments and demonstrate that this technique can model patient-specific tumors by using primary patient tissue. We assess intrinsic, extrinsic, and spatial tumorigenic phenotypes in bioprinted tissues and find that cellular proliferation, extracellular matrix deposition, and cellular migration are altered in response to extrinsic signals or therapies. Together, this work demonstrates that multi-cell-type bioprinted tissues can recapitulate aspects of in vivo neoplastic tissues and provide a manipulable system for the interrogation of multiple tumorigenic endpoints in the context of distinct tumor microenvironments.

Indexed as

BioprintingHumansPhenotypeTumor Microenvironment3D tumor modelsbreast cancerpancreatic cancerthree-dimensional bioprintingtumor microenvironment

Identifiers

PMID30650355
PMCPMC6366459

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.