Evidence map›Paper›PMID 32596380›Full record

ArticleBioMed research international2020

Iron-Chelating Agent Can Maintain Bone Homeostasis Disrupted by Iron Overload by Upregulating Wnt/Beta-Catenin Signaling.

Wei Xu, Ronghua Yu, Xiaodong Zhu, Zhikun Li, Jianjun Jia, Dachuan Li, Yu Chen, Xiangyang Zhang

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Wei XuDepartment of Orthopedics, TongRen Hospital, School of Medicine Shanghai Jiao Tong University, 1111 Xianxia Road, Shanghai 200336, China.
Ronghua YuDepartment of Orthopedics, TongRen Hospital, School of Medicine Shanghai Jiao Tong University, 1111 Xianxia Road, Shanghai 200336, China.
Xiaodong ZhuDepartment of Orthopedics, TongRen Hospital, School of Medicine Shanghai Jiao Tong University, 1111 Xianxia Road, Shanghai 200336, China.
Zhikun LiDepartment of Orthopedics, TongRen Hospital, School of Medicine Shanghai Jiao Tong University, 1111 Xianxia Road, Shanghai 200336, China.ORCID https://orcid.org/0000-0002-1732-5931
Jianjun JiaNo.7 College Team, PLA Naval Medical University, 800 Xiangyin Road, Shanghai 200443, China.
Dachuan LiNo.7 College Team, PLA Naval Medical University, 800 Xiangyin Road, Shanghai 200443, China.
Yu ChenDepartment of Orthopedics, TongRen Hospital, School of Medicine Shanghai Jiao Tong University, 1111 Xianxia Road, Shanghai 200336, China.
Xiangyang ZhangDepartment of Orthopedics, TongRen Hospital, School of Medicine Shanghai Jiao Tong University, 1111 Xianxia Road, Shanghai 200336, China.
Shanghai Jiao Tong University · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe incidence of osteoporotic fractures is increasing. In this study, we explored the activities of Wnt/

methodsWe established rat bipedal walking models (RBWM), and a portion of our RBWM rats were intraperitoneally injected with ferric ammonium citrate, normal saline, and deferoxamine. Bone mineral density was measured with a small animal in vivo imaging system. The protein levels of ferritin, TRAP-5B, RANKL, and OPG in serum were measured by the enzyme-linked immunosorbent assay (ELISA). Quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot were used to quantify the RNA and protein expression levels of certain regulators involved in Wnt/

resultsIn the present study, we established a rat bipedal walking model containing 32 bipedal rats, which were randomly classified into four groups, termed as NS, FAC, FAC+NS, and FAC+DFO. Those three experimental groups with FAC injection had significantly lower bone mineral density (BMD) than the control group NS (

conclusionThe osteoporosis could be caused by iron overload, which reduced the bone mineral density by disrupting the homeostasis of bone formation and absorption and attenuating the Wnt/

Indexed as

Bone and BonesAnimalsbeta CateninFemaleHomeostasisIronIron Chelating AgentsIron OverloadRatsRats, Sprague-DawleyUp-RegulationWalkingWnt Signaling Pathwaybeta CateninIronIron Chelating Agents

Identifiers

PMID32596380
PMCPMC7273370
OpenAlexW3031045753

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Registered trials

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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.