Evidence map›Paper›PMID 33303737›Full record

ArticleNature communications2020

Inhibition of protein glycosylation is a novel pro-angiogenic strategy that acts via activation of stress pathways.

Cuiling Zhong, Pin Li, Sulabha Argade, Lixian Liu, Anastasia Chilla', Wei Liang, Hong Xin, Brian Eliceiri, Biswa Choudhury, Napoleone Ferrara

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 36 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Cuiling ZhongDepartment of Pathology, University of California, San Diego, La Jolla, CA, 92093, USA.
Pin LiDepartment of Pathology, University of California, San Diego, La Jolla, CA, 92093, USA.
Sulabha ArgadeDepartment of GlycoAnalytics Core, University of California, San Diego, La Jolla, CA, 92093, USA.
Lixian LiuDepartment of Pathology, University of California, San Diego, La Jolla, CA, 92093, USA.
Anastasia Chilla'Department of Pathology, University of California, San Diego, La Jolla, CA, 92093, USA.
Wei LiangDepartment of Pathology, University of California, San Diego, La Jolla, CA, 92093, USA.
Hong XinDepartment of Pathology, University of California, San Diego, La Jolla, CA, 92093, USA.
Brian EliceiriDepartment of Surgery, University of California, San Diego, La Jolla, CA, 92093, USA.
Biswa ChoudhuryDepartment of GlycoAnalytics Core, University of California, San Diego, La Jolla, CA, 92093, USA.
Napoleone FerraraDepartment of Pathology, University of California, San Diego, La Jolla, CA, 92093, USA. nferrara@ucsd.edu.ORCID 0000-0002-7029-6375
University of California San Diego · US

Funding

Tissue repair, extracellular vesicular biogenesis, and the control of immune responsesR01GM140137 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELICEIRI, BRIAN P · 2020 to 2023
$1.8M
NIGMS NIH HHS R01 GM140137
6 · The paper itself

Abstract

Endothelial cell (EC) metabolism is thought to be one of the driving forces for angiogenesis. Here we report the identification of the hexosamine D-mannosamine (ManN) as an EC mitogen and survival factor for bovine and human microvascular EC, with an additivity with VEGF. ManN inhibits glycosylation in ECs and induces significant changes in N-glycan and O-glycan profiles. We further demonstrate that ManN and two N-glycosylation inhibitors stimulate EC proliferation via both JNK activation and the unfolded protein response caused by ER stress. ManN results in enhanced angiogenesis in a mouse skin injury model. ManN also promotes angiogenesis in a mouse hindlimb ischemia model, with accelerated limb blood flow recovery compared to controls. In addition, intraocular injection of ManN induces retinal neovascularization. Therefore, activation of stress pathways following inhibition of protein glycosylation can promote EC proliferation and angiogenesis and may represent a therapeutic strategy for treatment of ischemic disorders.

Indexed as

Neovascularization, PhysiologicStress, PhysiologicalAnimalsCattleCell ProliferationCells, CulturedDisease Models, AnimalEndoplasmic Reticulum Chaperone BiPEnzyme ActivationFemaleGlycosylationHeat-Shock ProteinsHexosaminesHindlimbHumansHuman Umbilical Vein Endothelial CellsEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsHexosaminesmannosamineProteinsTranscription Factor CHOPVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID33303737
PMCPMC7730427
OpenAlexW3112966599

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.