Evidence map›Paper›PMID 37493987›Full record

ArticleAngiogenesis2024

Phenotypic screening in Organ-on-a-Chip systems: a 1537 kinase inhibitor library screen on a 3D angiogenesis assay.

Camilla Soragni, Karla Queiroz, Chee Ping Ng, Arthur Stok, Thomas Olivier, Dora Tzagkaraki, Jeroen Heijmans, Johnny Suijker, Sander P M de Ruiter, Aleksandra Olczyk and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Angiogenesis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

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  9. Engineering in vitro vascular microsystems.Microsystems & nanoengineering · 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

16 authors at 1 institution in 1 country.

Camilla Soragni *MIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Karla Queiroz *MIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Chee Ping Ng *MIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Arthur StokMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Thomas OlivierMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Dora TzagkarakiMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Jeroen HeijmansMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Johnny SuijkerMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Sander P M de RuiterMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Aleksandra OlczykMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Marleen BokkersMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Frederik SchavemakerMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Sebastian J TrietschMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Henriëtte L LanzMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Paul VultoMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands.
Jos JooreMIMETAS BV, De Limes 7, 2342 DH, Oegstgeest, The Netherlands. j.joore@mimetas.com.
Mimetas (Netherlands) · NL

Funding

H2020 Marie Skłodowska-Curie Actions 765274
6 · The paper itself

Abstract

Modern drug development increasingly requires comprehensive models that can be utilized in the earliest stages of compound and target discovery. Here we report a phenotypic screening exercise in a high-throughput Organ-on-a-Chip setup. We assessed the inhibitory effect of 1537 protein kinase inhibitors in an angiogenesis assay. Over 4000 micro-vessels were grown under perfusion flow in microfluidic chips, exposed to a cocktail of pro-angiogenic factors and subsequently exposed to the respective kinase inhibitors. Efficacy of compounds was evaluated by reduced angiogenic sprouting, whereas reduced integrity of the main micro-vessel was taken as a measure for toxicity. The screen yielded 53 hits with high anti-angiogenicity and low toxicity, of which 44 were previously unassociated with angiogenic pathways. This study demonstrates that Organ-on-a-Chip models can be screened in high numbers to identify novel compounds and targets. This will ultimately reduce bias in early-stage drug development and increases probability to identify first in class compounds and targets for today's intractable diseases.

Indexed as

AngiogenesisAntineoplastic AgentsHumansMicrophysiological SystemsNeovascularization, PathologicProtein Kinase InhibitorsAntineoplastic AgentsProtein Kinase InhibitorsAngiogenesisHigh throughput screeningMicrophysiological systemsOrgan-on-a-ChipPhenotypic screeningProtein kinase inhibitors

Identifiers

PMID37493987
PMCPMC10881651
OpenAlexW4385264113

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.