Evidence map›Paper›PMID 24561529›Full record

ArticleOncogene2015

Angiogenin promotes tumoral growth and angiogenesis by regulating matrix metallopeptidase-2 expression via the ERK1/2 pathway.

M Miyake, S Goodison, A Lawton, E Gomes-Giacoia, C J Rosser

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

66 citing papers in PubMed, 100 citations in OpenAlex.

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  11. The role of angiogenin in bladder cancer: where are we in 2025?International urology and nephrology · 2025
    Review
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6 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

5 authors at 2 institutions in 1 country.

M MiyakeCancer Research Institute, MD Anderson Cancer Center, Orlando, FL, USA.
S Goodison1] Cancer Research Institute, MD Anderson Cancer Center, Orlando, FL, USA [2] Nonagen Bioscience Corp, Orlando, FL, USA.
A LawtonDepartment of Pathology, Orlando Health, Orlando, FL, USA.
E Gomes-GiacoiaCancer Research Institute, MD Anderson Cancer Center, Orlando, FL, USA.
C J Rosser1] Cancer Research Institute, MD Anderson Cancer Center, Orlando, FL, USA [2] Nonagen Bioscience Corp, Orlando, FL, USA.
Nonagen Bioscience (United States) · USOrlando Health · US

Funding

Towards a non-invasive molecular test for bladder cancerR01CA116161 · NCI · UNIVERSITY OF FLORIDA · PI GOODISON, STEVE · 2007 to 2019
$2.9M
NCI NIH HHS R01 CA116161
6 · The paper itself

Abstract

Tumor angiogenesis is essential for tumor growth and metastasis and is dependent on key angiogenic factors. Angiogenin (ANG), a 14.2-kDa polypeptide member of the RNase A superfamily, is an angiogenic protein that has been reported to be upregulated and associated with poor prognosis in some human cancers. The mechanisms through which aberrant ANG levels promote specific steps in tumor progression are unknown. Here, we show that ANG expression in human tissues is strongly correlated with an invasive cancer phenotype. We also show that ANG induces cellular survival, proliferation, endothelial tube formation and xenograft angiogenesis and growth. Novel mechanistic investigations revealed that ANG expression stimulated matrix metallopeptidase-2 (MMP2) expression through the phosphorylation of ERK1/2. Targeting ANG in vivo with N65828, a small-molecule inhibitor of the ribonucleolytic activity of human ANG, resulted in the diminution of xenograft tumoral growth through the inhibition of angiogenesis. Our findings support an unrecognized interplay between ANG, ERK1/2 and MMP2 that can impact tumor growth and progression. The targeting of ANG and associated factors could provide a novel strategy to inhibit tumor establishment and growth.

Indexed as

Gene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticMAP Kinase Signaling SystemAnimalsCell Line, TumorHeterograftsHumansMatrix Metalloproteinase 2MiceMice, Inbred BALB CMice, NudeMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Neoplasm MetastasisNeoplasm ProteinsNeoplasmsangiogeninMAPK1 protein, humanMatrix Metalloproteinase 2Mitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3MMP2 protein, humanNeoplasm ProteinsRibonuclease, Pancreatic

Identifiers

PMID24561529
PMCPMC4317372
OpenAlexW2008304553

What OpenQuestion holds

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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.