Evidence map›Paper›PMID 25814684›Full record

ReviewCirculation research2015

Endothelial cell metabolism in normal and diseased vasculature.

Guy Eelen, Pauline de Zeeuw, Michael Simons, Peter Carmeliet

Abstract readReview
In one paragraph

Review in Circulation research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 373 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
373citing papers in PubMed, 1 pooled it
23.0field-weighted citation impact, top 1% 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

373 citing papers in PubMed, 1 synthesis or guideline pooled it, 623 citations in OpenAlex.

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313 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

4 authors at 2 institutions in 2 countries.

Guy EelenFrom the Laboratory of Angiogenesis and Neurovascular Link, Vesalius Research Center, Department of Oncology, KU Leuven, Leuven, Belgium (G.E., P.d.Z., P.C.); Laboratory of Angiogenesis and Neurovascular Link, Vesalius Research Center, VIB, Leuven, Belgium (G.E., P.d.Z., P.C.); Yale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, New Haven, CT (M.S.); and Department of Cell Biology, Yale University School of Medicine, New Haven, CT (M.S.).
Pauline de ZeeuwFrom the Laboratory of Angiogenesis and Neurovascular Link, Vesalius Research Center, Department of Oncology, KU Leuven, Leuven, Belgium (G.E., P.d.Z., P.C.); Laboratory of Angiogenesis and Neurovascular Link, Vesalius Research Center, VIB, Leuven, Belgium (G.E., P.d.Z., P.C.); Yale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, New Haven, CT (M.S.); and Department of Cell Biology, Yale University School of Medicine, New Haven, CT (M.S.).
Michael SimonsFrom the Laboratory of Angiogenesis and Neurovascular Link, Vesalius Research Center, Department of Oncology, KU Leuven, Leuven, Belgium (G.E., P.d.Z., P.C.); Laboratory of Angiogenesis and Neurovascular Link, Vesalius Research Center, VIB, Leuven, Belgium (G.E., P.d.Z., P.C.); Yale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, New Haven, CT (M.S.); and Department of Cell Biology, Yale University School of Medicine, New Haven, CT (M.S.).
Peter CarmelietFrom the Laboratory of Angiogenesis and Neurovascular Link, Vesalius Research Center, Department of Oncology, KU Leuven, Leuven, Belgium (G.E., P.d.Z., P.C.); Laboratory of Angiogenesis and Neurovascular Link, Vesalius Research Center, VIB, Leuven, Belgium (G.E., P.d.Z., P.C.); Yale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, New Haven, CT (M.S.); and Department of Cell Biology, Yale University School of Medicine, New Haven, CT (M.S.). peter.carmeliet@vib-kuleuven.be.
Yale University · USVIB-KU Leuven Center for Cancer Biology · BE

Funding

Surgery / Physiology CoreP01HL107205 · NHLBI · YALE UNIVERSITY · PI SIMONS, MICHAEL · 2012 to 2022
$18.8M
Angiogensis and ischemiaR01HL053793 · NHLBI · YALE UNIVERSITY · PI SIMONS, MICHAEL · 1996 to 2017
$7.3M
Arteriogenesis and BranchingR01HL084619 · NHLBI · YALE UNIVERSITY · PI SIMONS, MICHAEL · 2007 to 2018
$6.7M
NHLBI NIH HHS HL053793NHLBI NIH HHS HL084619NHLBI NIH HHS P01 HL107205NHLBI NIH HHS R01 HL053793NHLBI NIH HHS R01 HL084619
6 · The paper itself

Abstract

Higher organisms rely on a closed cardiovascular circulatory system with blood vessels supplying vital nutrients and oxygen to distant tissues. Not surprisingly, vascular pathologies rank among the most life-threatening diseases. At the crux of most of these vascular pathologies are (dysfunctional) endothelial cells (ECs), the cells lining the blood vessel lumen. ECs display the remarkable capability to switch rapidly from a quiescent state to a highly migratory and proliferative state during vessel sprouting. This angiogenic switch has long been considered to be dictated by angiogenic growth factors (eg, vascular endothelial growth factor) and other signals (eg, Notch) alone, but recent findings show that it is also driven by a metabolic switch in ECs. Furthermore, these changes in metabolism may even override signals inducing vessel sprouting. Here, we review how EC metabolism differs between the normal and dysfunctional/diseased vasculature and how it relates to or affects the metabolism of other cell types contributing to the pathology. We focus on the biology of ECs in tumor blood vessel and diabetic ECs in atherosclerosis as examples of the role of endothelial metabolism in key pathological processes. Finally, current as well as unexplored EC metabolism-centric therapeutic avenues are discussed.

Indexed as

Amino AcidsAtherosclerosisCell MovementDiabetic AngiopathiesEndothelial CellsEndothelium, VascularEnergy MetabolismFatty AcidsGlucoseGlycation End Products, AdvancedHumansMorphogenesisNeoplasmsNeovascularization, PathologicNeovascularization, PhysiologicNitric OxideAmino AcidsFatty AcidsGlucoseGlycation End Products, AdvancedNitric OxideReactive Oxygen Speciesangiogenesisatherosclerosiscancerdiabetes mellitusendothelial metabolism

Identifiers

PMID25814684
PMCPMC4380230
OpenAlexW1966971152

What OpenQuestion holds

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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.