Evidence map›Paper›PMID 28238213›Full record

ReviewJournal of cellular and molecular medicine2017

Extracellular renalase protects cells and organs by outside-in signalling.

Yang Wang, Robert Safirstein, Heino Velazquez, Xiao-Jia Guo, Lindsay Hollander, John Chang, Tian-Min Chen, Jian-Jun Mu, Gary V Desir

Open access · goldAbstract readReview
In one paragraph

Review in Journal of cellular and molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 47 citations in OpenAlex.

  1. Low Renalase Levels in Newly Diagnosed CML: Dysregulation Sensitive to Modulation by Tyrosine Kinase Inhibitors.Pathophysiology : the official journal of the International Society for Pathophysiology · 2024
    Article
  2. Renalase alleviates salt-induced kidney necroptosis and inflammation.Hypertension research : official journal of the Japanese Society of Hypertension · 2024
    Article
  3. Review
  4. Renalase: a novel regulator of cardiometabolic and renal diseases.Hypertension research : official journal of the Japanese Society of Hypertension · 2022
    Review
  5. Inhibition of renalase drives tumour rejection by promoting T cell activation.European journal of cancer (Oxford, England : 1990) · 2022
    Article
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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

9 authors at 3 institutions in 2 countries.

Yang WangDepartment of Medicine, Veterans Affairs Connecticut Healthcare System, Yale University, New Haven, CT, USA.
Robert SafirsteinDepartment of Medicine, Veterans Affairs Connecticut Healthcare System, Yale University, New Haven, CT, USA.
Heino VelazquezDepartment of Medicine, Veterans Affairs Connecticut Healthcare System, Yale University, New Haven, CT, USA.
Xiao-Jia GuoDepartment of Medicine, Veterans Affairs Connecticut Healthcare System, Yale University, New Haven, CT, USA.
Lindsay HollanderDepartment of Medicine, Veterans Affairs Connecticut Healthcare System, Yale University, New Haven, CT, USA.
John ChangDepartment of Medicine, Veterans Affairs Connecticut Healthcare System, Yale University, New Haven, CT, USA.
Tian-Min ChenDepartment of Medicine, Veterans Affairs Connecticut Healthcare System, Yale University, New Haven, CT, USA.
Jian-Jun MuDepartment of Cardiology, First Affiliated Hospital of Medical School, Xi'an Jiaotong University, Xi'an, China.
Gary V DesirDepartment of Medicine, Veterans Affairs Connecticut Healthcare System, Yale University, New Haven, CT, USA.
VA Connecticut Healthcare System · USYale University · USFirst Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

Renal Physiology and Phenotyping CoreP30DK079310 · NIDDK · YALE UNIVERSITY · PI SOMLO, STEFAN · 2008 to 2022
$16.8M
NIDDK NIH HHS P30 DK079310
6 · The paper itself

Abstract

Renalase was discovered as a protein synthesized by the kidney and secreted in blood where it circulates at a concentration of approximately 3-5 μg/ml. Initial reports suggested that it functioned as an NAD(P)H oxidase and could oxidize catecholamines. Administration of renalase lowers blood pressure and heart rate and also protects cells and organs against ischaemic and toxic injury. Although renalase's protective effect was initially ascribed to its oxidase properties, a paradigm shift in our understanding of the cellular actions of renalase is underway. We now understand that, independent of its enzymatic properties, renalase functions as a cytokine that provides protection to cells, tissues and organs by interacting with its receptor to activate protein kinase B, JAK/STAT, and the mitogen-activated protein kinase pathways. In addition, recent studies suggest that dysregulated renalase signalling may promote survival of several tumour cells due to its capacity to augment expression of growth-related genes. In this review, we focus on the cytoprotective actions of renalase and its capacity to sustain cancer cell growth and also the translational opportunities these findings represent for the development of novel therapeutic strategies for organ injury and cancer.

Indexed as

Blood PressureCatecholaminesCytokinesHeart RateHumansKidneyMonoamine OxidaseNADPH OxidasesNeoplasmsOxidation-ReductionCatecholaminesCytokinesMonoamine OxidaseNADPH Oxidasesrenalasecell signallingimmune-oncologyischaemic injurymacrophagesrenalasesurvival factor

Identifiers

PMID28238213
PMCPMC5487909
OpenAlexW2590031259

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.