Evidence map›Paper›PMID 31489365›Full record

ArticleScience advances2019

A biomimetic pancreatic cancer on-chip reveals endothelial ablation via ALK7 signaling.

Duc-Huy T Nguyen, Esak Lee, Styliani Alimperti, Robert J Norgard, Alec Wong, Jake June-Koo Lee, Jeroen Eyckmans, Ben Z Stanger, Christopher S Chen

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed, 1 pooled it
8.1field-weighted citation impact, top 2% 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

103 citing papers in PubMed, 1 synthesis or guideline pooled it, 169 citations in OpenAlex.

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43 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.

Duc-Huy T NguyenDepartment of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0003-0805-8103
Esak LeeDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, USA.ORCID 0000-0002-5328-6677
Styliani AlimpertiDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Robert J NorgardDivision of Gastroenterology, Department of Medicine and Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0003-4245-6770
Alec WongDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, USA.
Jake June-Koo LeeDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA 02115, USA.ORCID 0000-0003-1348-4094
Jeroen EyckmansDepartment of Biomedical Engineering, Boston University, Boston, MA 02215, USA.ORCID 0000-0003-1475-8149
Ben Z StangerDivision of Gastroenterology, Department of Medicine and Abramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0003-0410-4037
Christopher S ChenDepartment of Chemical and Biomolecular Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0003-2445-8449
Boston University · USUniversity of Pennsylvania · USHarvard University · US

Funding

Tissue Chips for Rare Disease: Adding Timothy Syndrome to the HeLIVaSkCa platformUH3EB017103 · NIBIB · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI VUNJAK-NOVAKOVIC, GORDANA · 2014 to 2016
$7.1M
REGULATION OF ANGIOGENESIS BY MICROENVIRONMENTAL CUESR01EB000262 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI CHEN, CHRISTOPHER S · 2002 to 2023
$6.2M
A vascularized 3D biomimetic for islet function and physiologyUC4DK104196 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI CHEN, CHRISTOPHER S, GADUE, PAUL J · 2014 to 2016
$5.1M
NRSA Training CoreTL1TR001410 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KOTTON, DARRELL N. · 2015 to 2024
$4.3M
Multi-tissue platform for modeling systemic pathologiesUH3EB025765 · NIBIB · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI VUNJAK-NOVAKOVIC, GORDANA · 2019 to 2021
$4.0M
NCATS NIH HHS TL1 TR001410NIBIB NIH HHS R01 EB000262NIBIB NIH HHS UH3 EB017103NIBIB NIH HHS UH3 EB025765NIDDK NIH HHS UC4 DK104196
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) is an aggressive, lethal malignancy that invades adjacent vasculatures and spreads to distant sites before clinical detection. Although invasion into the peripancreatic vasculature is one of the hallmarks of PDAC, paradoxically, PDAC tumors also exhibit hypovascularity. How PDAC tumors become hypovascular is poorly understood. We describe an organotypic PDAC-on-a-chip culture model that emulates vascular invasion and tumor-blood vessel interactions to better understand PDAC-vascular interactions. The model features a 3D matrix containing juxtaposed PDAC and perfusable endothelial lumens. PDAC cells invaded through intervening matrix, into vessel lumen, and ablated the endothelial cells, leaving behind tumor-filled luminal structures. Endothelial ablation was also observed in in vivo PDAC models. We also identified the activin-ALK7 pathway as a mediator of endothelial ablation by PDAC. This tumor-on-a-chip model provides an important in vitro platform for investigating the process of PDAC-driven endothelial ablation and may provide a mechanism for tumor hypovascularity.

Indexed as

Activin Receptors, Type IAdenocarcinomaAnimalsBiomimeticsCarcinoma, Pancreatic DuctalCell LineCell Line, TumorEndothelial CellsHumansHuman Umbilical Vein Endothelial CellsMiceNeoplasm InvasivenessPancreatic NeoplasmsSignal TransductionActivin Receptors, Type IACVR1C protein, human

Identifiers

PMID31489365
PMCPMC6713506
OpenAlexW2970097127

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.