Evidence map›Paper›PMID 37797407›Full record

ArticleAdvanced healthcare materials2024

Utilization of an Artery-on-a-Chip to Unravel Novel Regulators and Therapeutic Targets in Vascular Diseases.

Valentina Paloschi, Jessica Pauli, Greg Winski, Zhiyuan Wu, Zhaolong Li, Lorenzo Botti, Sandro Meucci, Pierangelo Conti, Felix Rogowitz, Nadiya Glukha and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Advanced healthcare materials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

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  16. Long Non-Coding RNA Function in Smooth Muscle Cell Plasticity and Atherosclerosis.Arteriosclerosis, thrombosis, and vascular biology · 2025
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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

20 authors at 9 institutions in 6 countries.

Valentina PaloschiDepartment for Vascular and Endovascular Surgery, Technical University of Munich, 80333, Munich, Germany.ORCID 0000-0002-5778-8981
Jessica PauliDepartment for Vascular and Endovascular Surgery, Technical University of Munich, 80333, Munich, Germany.
Greg WinskiDepartment of Medicine, Cardiovascular Unit, Karolinska Institute, 171 77, Stockholm, Sweden.
Zhiyuan WuDepartment for Vascular and Endovascular Surgery, Technical University of Munich, 80333, Munich, Germany.
Zhaolong LiDepartment for Vascular and Endovascular Surgery, Technical University of Munich, 80333, Munich, Germany.
Lorenzo BottiDepartment of Engineering and Applied Sciences, University of Bergamo, Bergamo, 24129, Italy.
Sandro MeucciMicronit Microtechnologies, Enschede, 15 7521, The Netherlands.
Pierangelo ContiDepartment of Engineering and Applied Sciences, University of Bergamo, Bergamo, 24129, Italy.
Felix RogowitzFLUIGENT Deutschland GmbH, 07743, Jena, Germany.
Nadiya GlukhaDepartment for Vascular and Endovascular Surgery, Technical University of Munich, 80333, Munich, Germany.
Nora HummelDepartment for Vascular and Endovascular Surgery, Technical University of Munich, 80333, Munich, Germany.
Albert BuschDepartment for Vascular and Endovascular Surgery, Technical University of Munich, 80333, Munich, Germany.
Ekaterina ChernogubovaDepartment of Medicine, Cardiovascular Unit, Karolinska Institute, 171 77, Stockholm, Sweden.
Hong JinDepartment of Medicine, Cardiovascular Unit, Karolinska Institute, 171 77, Stockholm, Sweden.
Nadja SachsDepartment for Vascular and Endovascular Surgery, Technical University of Munich, 80333, Munich, Germany.
Hans-Henning EcksteinDepartment for Vascular and Endovascular Surgery, Technical University of Munich, 80333, Munich, Germany.
Anne DueckGerman Center for Cardiovascular Research DZHK, Partner Site Munich Heart Alliance, 80336, Berlin, Germany.
Reinier A BoonDepartment of Physiology, Amsterdam Cardiovascular Sciences (ACS), Amsterdam UMC, VU University Medical Center, Amsterdam, 1081 HV, The Netherlands.
Andreas R BauschDepartment of Cellular Biophysics, Technical University of Munich, 80333, Munich, Germany.
Lars MaegdefesselDepartment for Vascular and Endovascular Surgery, Technical University of Munich, 80333, Munich, Germany.
Technical University of Munich · DEKarolinska Institutet · SEGerman Centre for Cardiovascular Research · DEUniversity of Bergamo · ITChinese Academy of Medical Sciences & Peking Union Medical College · CNFluigent (France) · FRGoethe University Frankfurt · DEMicronit Microfluidics (Netherlands) · NLUniversity Hospital Carl Gustav Carus · DE

Funding

Computational and functional strategies to decipher lncRNAs in human atherosclerosisR01HL150359 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LI, MINGYAO, REILLY, MUREDACH P · 2020 to 2023
$2.7M
NHLBI NIH HHS R01 HL150359NIH HHS 1R011HL150359-01
6 · The paper itself

Abstract

In this study, organ-on-chip technology is used to develop an in vitro model of medium-to-large size arteries, the artery-on-a-chip (AoC), with the objective to recapitulate the structure of the arterial wall and the relevant hemodynamic forces affecting luminal cells. AoCs exposed either to in vivo-like shear stress values or kept in static conditions are assessed to generate a panel of novel genes modulated by shear stress. Considering the crucial role played by shear stress alterations in carotid arteries affected by atherosclerosis (CAD) and abdominal aortic aneurysms (AAA) disease development/progression, a patient cohort of hemodynamically relevant specimens is utilized, consisting of diseased and non-diseased (internal control) vessel regions from the same patient. Genes activated by shear stress follow the same expression pattern in non-diseased segments of human vessels. Single cell RNA sequencing (scRNA-seq) enables to discriminate the unique cell subpopulations between non-diseased and diseased vessel portions, revealing an enrichment of flow activated genes in structural cells originating from non-diseased specimens. Furthermore, the AoC served as a platform for drug-testing. It reproduced the effects of a therapeutic agent (lenvatinib) previously used in preclinical AAA studies, therefore extending the understanding of its therapeutic effect through a multicellular structure.

Indexed as

Aortic Aneurysm, AbdominalAtherosclerosisArteriesDisease ProgressionHumansLab-On-A-Chip Devicesaortic aneurysmsarteries-on-a-chipatherosclerosisendothelial cellssmooth muscle cellsvascular diseases

Identifiers

PMID37797407
PMCPMC11468405
OpenAlexW4387392060

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.