Evidence map›Paper›PMID 23118343›Full record

ArticleDisease models & mechanisms2013

Endogenous ribosomal protein L29 (RPL29): a newly identified regulator of angiogenesis in mice.

Dylan T Jones, Tanguy Lechertier, Louise E Reynolds, Richard Mitter, Stephen D Robinson, Catherine B Kirn-Safran, Kairbaan M Hodivala-Dilke

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

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  12. Genomic sites hypersensitive to ultraviolet radiation.Proceedings of the National Academy of Sciences of the United States of America · 2019
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  15. Review
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

7 authors at 5 institutions in 2 countries.

Dylan T JonesCentre for Tumour Biology, Barts Cancer Institute-a CR-UK Centre of Excellence, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London, EC1M 6BQ, UK. dylan.jones@oncology.ox.ac.uk
Tanguy Lechertier
Louise E Reynolds
Richard Mitter
Stephen D Robinson
Catherine B Kirn-Safran
Kairbaan M Hodivala-Dilke
Queen Mary University of London · GBCancer Research UK · GBMRC Weatherall Institute of Molecular Medicine · GBUniversity of Delaware · USUniversity of East Anglia · GB

Funding

VALGUS BRACING FOR MEDIAL LAXITY IN PATIENTS WITH OSTEOARTHRITISP20RR016458 · NCRR · UNIVERSITY OF DELAWARE · PI RUDOLPH, KATHERINE S · 2002 to 2011
$18.9M
Cancer Research UK 12007Cancer Research UK C8212_A12007Medical Research Council G0901609NCRR NIH HHS P20 RR016458NCRR NIH HHS P20-RR016458
6 · The paper itself

Abstract

Cellular ribosomal protein L29 (RPL29) is known to be important in protein synthesis, but its function during angiogenesis has never been described before. We have shown previously that mice lacking β3-integrins support enhanced tumour angiogenesis and, therefore, deletion of endothelial αvβ3 can provide a method for discovery of novel regulators of tumour angiogenesis. Here, we describe significant upregulation of RPL29 in β3-null endothelial cells at both the mRNA and protein level. Ex vivo, we show that VEGF-stimulated microvessel sprouting was reduced significantly in Rpl29-heterozygous and Rpl29-null aortic ring assays compared with wild-type controls. Moreover, we provide in vivo evidence that RPL29 can regulate tumour angiogenesis. Tumour blood vessel density in subcutaneously grown Lewis lung carcinomas was reduced significantly in Rpl29-mutant mice. Additionally, depletion of Rpl29 using RNA interference inhibited VEGF-induced aortic ring sprouting, suggesting that anti-RPL29 strategies might have anti-angiogenic potential. Overall, our results identify that loss or depletion of RPL29 can reduce angiogenesis in vivo and ex vivo.

Indexed as

AnimalsAorta, ThoracicCarcinoma, Lewis LungEndothelial CellsGene ExpressionIntegrin alphaVbeta3MaleMiceMice, Inbred C57BLMice, KnockoutNeovascularization, PathologicNeovascularization, PhysiologicRibosomal ProteinsRNA-Binding ProteinsRNA InterferenceRNA, MessengerIntegrin alphaVbeta3Ribosomal ProteinsRNA-Binding ProteinsRNA, MessengerRpl29 protein, mouseVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouse

Identifiers

PMID23118343
PMCPMC3529344
OpenAlexW2131756564

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.