Evidence map›Paper›PMID 35701603›Full record

ArticleCommunications biology2022

Nox4 expression in osteo-progenitors controls bone development in mice during early life.

Jin-Ran Chen, Oxana P Lazarenko, Michael L Blackburn, Jennifer F Chen, Christopher E Randolph, Jovanny Zabaleta, Katrin Schroder, Kim B Pedersen, Martin J J Ronis

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. 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
1.3field-weighted citation impact, top 21% 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, 17 citations in OpenAlex.

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  11. Halofuginone Inhibits Osteoclastogenesis and Enhances Osteoblastogenesis by Regulating Th17/Treg Cell Balance in Multiple Myeloma Mice with Bone Lesions.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 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

9 authors at 6 institutions in 2 countries.

Jin-Ran ChenArkansas Children's Nutrition Center, Little Rock, AR, 72202, USA. chenjinran@uams.edu.ORCID 0000-0001-6984-5878
Oxana P LazarenkoArkansas Children's Nutrition Center, Little Rock, AR, 72202, USA.
Michael L BlackburnArkansas Children's Nutrition Center, Little Rock, AR, 72202, USA.
Jennifer F ChenUndergraduate Pre-Medical Program, University of Arkansas at Fayetteville, Fayetteville, AR, 72701, USA.
Christopher E RandolphCenter for Translational Pediatric Research, Arkansas Children's Research Institute, Little Rock, AR, 72202, USA.
Jovanny ZabaletaDepartment of Pharmacology and Experimental Therapeutics, Louisiana State University Health Sciences Center, New Orleans, LA, 70112, USA.
Katrin SchroderInstitute of Physiology I, Goethe-University, Frankfurt, Germany.ORCID 0000-0002-3099-526X
Kim B PedersenDepartment of Interdisciplinary Oncology (DIO), Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, Louisiana Cancer Research Center, New Orleans, LA, 70112, USA.
Martin J J RonisDepartment of Interdisciplinary Oncology (DIO), Stanley S. Scott Cancer Center, Louisiana State University Health Sciences Center, Louisiana Cancer Research Center, New Orleans, LA, 70112, USA. mronis@lsuhsc.edu.ORCID 0000-0002-0116-3771
Arkansas Children's Nutrition Center · USLouisiana State University · USUniversity of Arkansas Medical Center · USArkansas Children's Hospital · USGoethe University Frankfurt · DELouisiana State University Health Sciences Center New Orleans · US

Funding

The role of oxidative stress in alcohol-induced osteopeniaR37AA018282 · NIAAA · LSU HEALTH SCIENCES CENTER · PI RONIS, MARTIN J J · 2016 to 2025
$4.7M
Alcohol-Induced Bone Resorption: The Role of Oxidative StressR01AA018282 · NIAAA · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI RONIS, MARTIN J J · 2009 to 2013
$1.7M
NIAAA NIH HHS R01 AA018282NIAAA NIH HHS R37 AA018282
6 · The paper itself

Abstract

Tightly regulated and cell-specific NADPH-oxidases (Nox) represent one of the major sources of reactive oxygen species (ROS) signaling molecules that are involved in tissue development and stem cell self-renewal. We have characterized the role of Nox4 in osteo-progenitors during postnatal bone development. Nox4 expression in bone and ROS generation were increased during early osteoblast differentiation and bone development. Stromal osteoblastic cell self-renewal, proliferation and ROS production were significantly lower in samples from whole-body Nox4 knockout mice (Nox4

Indexed as

Bone DevelopmentNADPH Oxidase 4OsteogenesisAnimalsFemaleMaleMiceMice, KnockoutReactive Oxygen SpeciesNADPH Oxidase 4Nox4 protein, mouseReactive Oxygen Species

Identifiers

PMID35701603
PMCPMC9198054
OpenAlexW4282824150

What OpenQuestion holds

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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.