Evidence map›Paper›PMID 27480772›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2016

The Retinoid Agonist Tazarotene Promotes Angiogenesis and Wound Healing.

Ayman Al Haj Zen, Dorota A Nawrot, Alison Howarth, Andrea Caporali, Daniel Ebner, Aude Vernet, Jurgen E Schneider, Shoumo Bhattacharya

Open access · greenAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 44 citations in OpenAlex.

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  14. Retinoic acid signaling in vascular development.Genesis (New York, N.Y. : 2000) · 2019
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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

8 authors at 3 institutions in 1 country.

Ayman Al Haj ZenWellcome Trust Centre For Human Genetics, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Dorota A NawrotWellcome Trust Centre For Human Genetics, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Alison HowarthTarget Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Andrea CaporaliUniversity/BHF Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
Daniel EbnerTarget Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Aude VernetWellcome Trust Centre For Human Genetics, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Jurgen E SchneiderWellcome Trust Centre For Human Genetics, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Shoumo BhattacharyaWellcome Trust Centre For Human Genetics, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
University of Oxford · GBCentre for Human Genetics · GBUniversity of Edinburgh · GB

Funding

ATHEROGENIC &ANTIATHEROGENIC LIPOPROTEINS IN CADF32HL008004 · NHLBI · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI WILSON, PAUL R · 1989 to 1990
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HUMAN PULMONARY SURFACTANT PROTEINS IN MILKF32HL009003 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI YARUS, SINAI · 1994 to 1996
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PERTUSSIS ADENYLATE CYCLASE: EFFECTS ON BLOOD CELLSK08HL001150 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CONFER, DENNIS L · 1985 to 1987
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British Heart Foundation CH/09/003British Heart Foundation FS/11/50/29038British Heart Foundation FS/11/52/29018British Heart Foundation FS/14/7/30574British Heart Foundation RE/08/004/23915British Heart Foundation RE/13/1/30181British Heart Foundation RG/10/17/28553British Heart Foundation RG/11/1/28684Wellcome Trust 090207/Z/09/ZWellcome Trust 090532/Z/09/Z
6 · The paper itself

Abstract

Therapeutic angiogenesis is a major goal of regenerative medicine, but no clinically approved small molecule exists that enhances new blood vessel formation. Here we show, using a phenotype-driven high-content imaging screen of an annotated chemical library of 1,280 bioactive small molecules, that the retinoid agonist Tazarotene, enhances in vitro angiogenesis, promoting branching morphogenesis, and tubule remodeling. The proangiogenic phenotype is mediated by retinoic acid receptor but not retinoic X receptor activation, and is characterized by secretion of the proangiogenic factors hepatocyte growth factor, vascular endothelial growth factor, plasminogen activator, urokinase and placental growth factor, and reduced secretion of the antiangiogenic factor pentraxin-3 from adjacent fibroblasts. In vivo, Tazarotene enhanced the growth of mature and functional microvessels in Matrigel implants and wound healing models, and increased blood flow. Notably, in ear punch wound healing model, Tazarotene promoted tissue repair characterized by rapid ear punch closure with normal-appearing skin containing new hair follicles, and maturing collagen fibers. Our study suggests that Tazarotene, an FDA-approved small molecule, could be potentially exploited for therapeutic applications in neovascularization and wound healing.

Indexed as

Angiogenesis Inducing AgentsAnimalsCell ProliferationCells, CulturedDisease Models, AnimalFibroblastsHumansHuman Umbilical Vein Endothelial CellsMiceNicotinic AcidsReceptors, Retinoic AcidRetinoidsSignal TransductionWound HealingAngiogenesis Inducing AgentsNicotinic AcidsReceptors, Retinoic AcidRetinoidstazarotene

Identifiers

PMID27480772
PMCPMC5112045
OpenAlexW2506444115

What OpenQuestion holds

Textmetadata
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.