Evidence map›Paper›PMID 23143660›Full record

ArticleAngiogenesis2013

Ribonuclease 4 protects neuron degeneration by promoting angiogenesis, neurogenesis, and neuronal survival under stress.

Shuping Li, Jinghao Sheng, Jamie K Hu, Wenhao Yu, Hiroko Kishikawa, Miaofen G Hu, Kaori Shima, David Wu, Zhengping Xu, Winnie Xin and 4 more

Open access · greenAbstract read
In one paragraph

Article in Angiogenesis, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

48 citing papers in PubMed, 63 citations in OpenAlex.

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  7. Genomic structural variation contributes to evolved changes in gene expression in high-altitude Tibetan sheep.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

14 authors at 7 institutions in 3 countries.

Shuping LiMolecular Oncology Research Institute, Tufts Medical Center, 800 Washington Street, Box 5069, Boston, MA 02111, USA.
Jinghao Sheng
Jamie K Hu
Wenhao Yu
Hiroko Kishikawa
Miaofen G Hu
Kaori Shima
David Wu
Zhengping Xu
Winnie Xin
Katherine B Sims
John E Landers
Robert H Brown
Guo-fu Hu
Molecular Oncology (United States) · USCenter for Human Genetics · USTufts Medical Center · USUniversity of Massachusetts Chan Medical School · USZhejiang University · CNKagoshima University · JPUniversity of Washington · US

Funding

Identification of genes causative for familial ALS gene using exome sequencingR01NS073873 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LANDERS, JOHN E · 2011 to 2019
$4.6M
The mechanism of angiogenin-induced angiogenesisR01CA105241 · NCI · TUFTS MEDICAL CENTER · PI HU, GUO-FU · 2005 to 2015
$2.8M
Angiogenin in ALS Pathobiology and TherapyR01NS065237 · NINDS · TUFTS MEDICAL CENTER · PI HU, GUO-FU · 2010 to 2014
$1.8M
NCI NIH HHS R01 CA105241NINDS NIH HHS R01 NS 065237NINDS NIH HHS R01 NS065237NINDS NIH HHS R01 NS073873
6 · The paper itself

Abstract

Altered RNA processing is an underlying mechanism of amyotrophic lateral sclerosis (ALS). Missense mutations in a number of genes involved in RNA function and metabolisms are associated with ALS. Among these genes is angiogenin (ANG), the fifth member of the vertebrate-specific, secreted ribonuclease superfamily. ANG is an angiogenic ribonuclease, and both its angiogenic and ribonucleolytic activities are important for motor neuron health. Ribonuclease 4 (RNASE4), the fourth member of this superfamily, shares the same promoters with ANG and is co-expressed with ANG. However, the biological role of RNASE4 is unknown. To determine whether RNASE4 is involved in ALS pathogenesis, we sequenced the coding region of RNASE4 in ALS and control subjects and characterized the angiogenic, neurogenic, and neuroprotective activities of RNASE4 protein. We identified an allelic association of SNP rs3748338 with ALS and demonstrated that RNASE4 protein is able to induce angiogenesis in in vitro, ex vivo, and in vivo assays. RNASE4 also induces neural differentiation of P19 mouse embryonal carcinoma cells and mouse embryonic stem cells. Moreover, RNASE4 not only stimulates the formation of neurofilaments from mouse embryonic cortical neurons, but also protects hypothermia-induced degeneration. Importantly, systemic treatment with RNASE4 protein slowed weight loss and enhanced neuromuscular function of SOD1 (G93A) mice.

Indexed as

Neovascularization, PhysiologicNeurogenesisAnimalsBase SequenceCell LineDNA PrimersHumansIn Situ HybridizationMicePolymerase Chain ReactionPolymorphism, GeneticRibonucleasesDNA Primersribonuclease 4Ribonucleases

Identifiers

PMID23143660
PMCPMC3582744
OpenAlexW1997348859

What OpenQuestion holds

Textmetadata
LicenceTDM
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.