Evidence map›Paper›PMID 25774923›Full record

ArticlePloS one2015

RETRACTED: Effects of iron overload on the bone marrow microenvironment in mice.

Yuchen Zhang, Wenjing Zhai, Mingfeng Zhao, Deguan Li, Xiao Chai, Xiaoli Cao, Juanxia Meng, Jie Chen, Xia Xiao, Qing Li and 3 more

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in PloS one, 2015. 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 It has been retracted, and should not be counted.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 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 82 citations in OpenAlex.

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  17. EnvIRONmental Aspects in Myelodysplastic Syndrome.International journal of molecular sciences · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 1 country.

Yuchen ZhangDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Wenjing ZhaiDepartment of Stem Cells Transplantation, Blood Disease Hospital of Chinese Academy of Medical Sciences, Tianjin, China.
Mingfeng ZhaoDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Deguan LiKey Lab of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine, Academy of Medical Science and Peking Union Medical College, Tianjin, China.
Xiao ChaiDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Xiaoli CaoDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Juanxia MengDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Jie ChenDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Xia XiaoDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Qing LiDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Juan MuDepartment of Hematology, Tianjin First Central Hospital, Tianjin, China.
Jichun ShenDepartment of Hematology, Affiliated Hospital of Logistics University of People's Armed Police Force, Tianjin, China.
Aimin MengKey Lab of Radiation Medicine and Molecular Nuclear Medicine, Institute of Radiation Medicine, Academy of Medical Science and Peking Union Medical College, Tianjin, China.
Tianjin Medical University · CNTianjin First Center Hospital · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNInstitute of Hematology & Blood Diseases Hospital · CNLogistics University of People's Armed Police Force · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveUsing a mouse model, Iron Overload (IO) induced bone marrow microenvironment injury was investigated, focusing on the involvement of reactive oxygen species (ROS).

methodsMice were intraperitoneally injected with iron dextran (12.5, 25, or 50 mg) every three days for two, four, and six week durations. Deferasirox(DFX)125 mg/ml and N-acetyl-L-cysteine (NAC) 40 mM were co-administered. Then, bone marrow derived mesenchymal stem cells (BM-MSCs) were isolated and assessed for proliferation and differentiation ability, as well as related gene changes. Immunohistochemical analysis assessed the expression of haematopoietic chemokines. Supporting functions of BM-MSCs were studied by co-culture system.

resultsIn IO condition (25 mg/ml for 4 weeks), BM-MSCs exhibited proliferation deficiencies and unbalanced osteogenic/adipogenic differentiation. The IO BM-MSCs showed a longer double time (2.07±0.14 days) than control (1.03±0.07 days) (P<0.05). The immunohistochemical analysis demonstrated that chemokine stromal cell-derived factor-1, stem cell factor -1, and vascular endothelial growth factor-1 expression were decreased. The co-cultured system demonstrated that bone marrow mononuclear cells (BMMNCs) co-cultured with IO BM-MSCs had decreased colony forming unit (CFU) count (p<0.01), which indicates IO could lead to decreased hematopoietic supporting functions of BM-MSCs. This effect was associated with elevated phosphatidylinositol 3 kinase (PI3K) and reduced of Forkhead box protein O3 (FOXO3) mRNA expression, which could induce the generation of ROS. Results also demonstrated that NAC or DFX treatment could partially attenuate cell injury and inhibit signaling pathway striggered by IO.

conclusionThese results demonstrated that IO can impair the bone marrow microenvironment, including the quantity and quality of BM-MSCs.

Indexed as

Cellular MicroenvironmentAdipogenesisAnimalsBone MarrowCell DifferentiationCell ProliferationCells, CulturedCoculture TechniquesCytokinesDisease Models, AnimalForkhead Box Protein O3Forkhead Transcription FactorsGene Expression RegulationHematopoietic Stem CellsIron OverloadMaleCytokinesForkhead Box Protein O3Forkhead Transcription FactorsFoxO3 protein, mousePhosphatidylinositol 3-KinasesReactive Oxygen Species

Identifiers

PMID25774923
PMCPMC4361683
OpenAlexW2080287792

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.