Evidence map›Paper›PMID 36914692›Full record

ArticleNPJ Regenerative medicine2023

VEGF dose controls the coupling of angiogenesis and osteogenesis in engineered bone.

Andrea Grosso, Alexander Lunger, Maximilian G Burger, Priscilla S Briquez, Francesca Mai, Jeffrey A Hubbell, Dirk J Schaefer, Andrea Banfi, Nunzia Di Maggio

Open access · goldFull text read
In one paragraph

Article in NPJ Regenerative medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
8.3field-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

50 citing papers in PubMed, 54 citations in OpenAlex.

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  13. Effects ofAnimals : an open access journal from MDPI · 2026
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  16. Bio-OssFrontiers in bioengineering and biotechnology · 2026
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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

9 authors at 4 institutions in 4 countries.

Andrea Grosso *Regenerative Angiogenesis Laboratory, Department of Biomedicine, Basel University Hospital and University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Alexander Lunger *Regenerative Angiogenesis Laboratory, Department of Biomedicine, Basel University Hospital and University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Maximilian G Burger *Regenerative Angiogenesis Laboratory, Department of Biomedicine, Basel University Hospital and University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Priscilla S BriquezPritzker School of Molecular Engineering, University of Chicago, 5640 S Ellis Ave, Chicago, IL, 60637, USA.ORCID http://orcid.org/0000-0002-4680-9636
Francesca MaiRegenerative Angiogenesis Laboratory, Department of Biomedicine, Basel University Hospital and University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Jeffrey A HubbellPritzker School of Molecular Engineering, University of Chicago, 5640 S Ellis Ave, Chicago, IL, 60637, USA.
Dirk J SchaeferRegenerative Angiogenesis Laboratory, Department of Biomedicine, Basel University Hospital and University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland.
Andrea Banfi *Regenerative Angiogenesis Laboratory, Department of Biomedicine, Basel University Hospital and University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland. Andrea.Banfi@usb.ch.
Nunzia Di Maggio *Regenerative Angiogenesis Laboratory, Department of Biomedicine, Basel University Hospital and University of Basel, Hebelstrasse 20, 4031, Basel, Switzerland. Nunzia.Dimaggio@usb.ch.
University of Basel · CHUniversity Hospital of Basel · CHUniversity Medical Center Freiburg · DEUniversity of Chicago · US

Funding

EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 801159EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 874790Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) 182357Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) PMPDP3-158312
6 · The paper itself

Abstract

Vascular endothelial growth factor-A (VEGF) physiologically regulates both angiogenesis and osteogenesis, but its application in bone tissue engineering led to contradictory outcomes. A poorly understood aspect is how VEGF dose impacts the coordination between these two processes. Taking advantage of a unique and highly tunable platform, here we dissected the effects of VEGF dose over a 1,000-fold range in the context of tissue-engineered osteogenic grafts. We found that osteo-angiogenic coupling is exquisitely dependent on VEGF dose and that only a tightly defined dose range could stimulate both vascular invasion and osteogenic commitment of progenitors, with significant improvement in bone formation. Further, VEGF dose regulated Notch1 activation and the induction of a specific pro-osteogenic endothelial phenotype, independently of the promotion of vascular invasion. Therefore, in a therapeutic perspective, fine-tuning of VEGF dose in the signaling microenvironment is key to ensure physiological coupling of accelerated vascular invasion and improved bone formation.

Identifiers

PMID36914692
PMCPMC10011536
OpenAlexW4324128929

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read159
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.