Evidence map›Paper›PMID 25995969›Full record

ArticleJournal of stem cell research & therapy2014

Delivering Oxidation Resistance-1 (OXR1) to Mouse Kidney by Genetic Modified Mesenchymal Stem Cells Exhibited Enhanced Protection against Nephrotoxic Serum Induced Renal Injury and Lupus Nephritis.

Yajuan Li, Wei Li, Chu Liu, Mei Yan, Indu Raman, Yong Du, Xiangdong Fang, Xin J Zhou, Chandra Mohan, Quan-Zhen Li

Open access · greenAbstract read
In one paragraph

Article in Journal of stem cell research & therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

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  18. TLDc proteins: new players in the oxidative stress response and neurological disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2017
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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

10 authors at 1 institution in 1 country.

Yajuan LiLaboratory of Disease Genomics and Individualized Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100029, China ; Department of Immunology and Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Wei LiKey Laboratory of Medical Genetics, Wenzhou Medical University School of Laboratory Medicine & Life Science, Wenzhou, 325035, China.
Chu LiuKey Laboratory of Medical Genetics, Wenzhou Medical University School of Laboratory Medicine & Life Science, Wenzhou, 325035, China.
Mei YanDepartment of Immunology and Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Indu RamanDepartment of Immunology and Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Yong DuDepartment of Biomedical Engineering, University of Houston, Houston, TX, 77204, USA.
Xiangdong FangLaboratory of Disease Genomics and Individualized Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100029, China.
Xin J ZhouRenal Path Diagnostics, Pathologist BioMedical Laboratories, Lewisville, TX, 75067, USA.
Chandra MohanDepartment of Biomedical Engineering, University of Houston, Houston, TX, 77204, USA.
Quan-Zhen LiKey Laboratory of Medical Genetics, Wenzhou Medical University School of Laboratory Medicine & Life Science, Wenzhou, 325035, China ; Department of Immunology and Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Beijing Institute of Genomics · CN

Funding

SLAM Genes-from Mouse to ManP50AR055503 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI KARP, DAVID R · 2007 to 2011
$8.3M
IMMUNOGENETICS--TARGET ORGAN DAMAGE IN IMMUNE NEPHRITISR01AR050812 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI MOHAN, CHANDRA · 2003 to 2012
$3.2M
Tissue Kallikrein In Immune Mediated NephritisR03AR055778 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI LI, QUAN-ZHEN · 2009 to 2011
$232k
NIAMS NIH HHS P50 AR055503NIAMS NIH HHS R01 AR050812NIAMS NIH HHS R03 AR055778
6 · The paper itself

Abstract

objectiveTo elucidate the role of oxidation resistance 1 (OXR1) gene. Oxidative stress plays a pivotal role in pathogenesis of immune-mediated nephritis. Recently we identified oxidation resistance 1 (OXR1) is conventionally expressed in eukaryotes and has an ability to prevent oxidative damage caused by various oxidative stresses. However the protective effect of OXR1 in immune-associated inflammatory response and oxidative damage is not clear and will be investigated in this study.

methodsWe utilized mesenchymal stem cells (MSCs) as vehicles to carry OXR1 into the injured kidneys of nephritis model mice and investigated the influence of

resultsCompared with control mice, hOXR1-MSCs administration showed significantly decreased blood urea nitrogen (BUN), proteinuria and ameliorated renal pathological damage. hOXR1-MSCs transplantation significantly reduced macrophage and T lymphocyte infiltration by inhibiting the expression of CCL2, CCL7, IL-1β, IL-6 and NFκB in mouse kidney. Moreover, hOXR1-MSCs prevented hydrogen peroxide (H

conclusionOXR1-MSCs transplantation may exert a certain protective effect on nephritis by suppressing inflammation and oxidative stress.

Indexed as

apoptosisinflammationlupus nephritismesenchymal stem cellOxidation resistance 1oxidative stress

Identifiers

PMID25995969
PMCPMC4435960
OpenAlexW2329463175

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.