Evidence map›Paper›PMID 27191651›Full record

ArticleOncotarget2016

Mesenchymal stem cells in combination with erythropoietin repair hyperoxia-induced alveoli dysplasia injury in neonatal mice via inhibition of TGF-β1 signaling.

Yun Luan, Luan Zhang, Sun Chao, Xiaoli Liu, Kaili Li, Yibiao Wang, Zhaohua Zhang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Complex roles of TGF-β signaling pathways in lung development and bronchopulmonary dysplasia.American journal of physiology. Lung cellular and molecular physiology · 2023
    Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Spatial and temporal expression of SP-B and TGF-β1 in hyperoxia-induced neonatal rat lung injury.International journal of clinical and experimental pathology · 2018
    Article
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

7 authors at 1 institution in 1 country.

Yun LuanCentral Research Laboratory, The Second Hospital of Shandong University, Jinan, China.
Luan ZhangDepartment of Pediatrics, The Second Hospital of Shandong University, Jinan, China.
Sun ChaoCentral Research Laboratory, The Second Hospital of Shandong University, Jinan, China.
Xiaoli LiuDepartment of Hematology, The Second Hospital of Shandong University, Jinan, China.
Kaili LiCentral Research Laboratory, The Second Hospital of Shandong University, Jinan, China.
Yibiao WangDepartment of Pediatrics, The Second Hospital of Shandong University, Jinan, China.
Zhaohua ZhangDepartment of Pediatrics, The Second Hospital of Shandong University, Jinan, China.
Second Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study is to investigate the protection effects of bone marrow mesenchymal stem cells (MSCs) in combination with EPO against hyperoxia-induced bronchopulmonary dysplasia (BPD) injury in neonatal mice. BPD model was prepared by continuous high oxygen exposure, 1×106 bone marrow MSCs and 5000U/kg recombinant human erythropoietin (EPO) were injected respectively. Results showed that administration of MSCs, EPO especially MSCs+EPO significant attenuated hyperoxia-induced lung damage with a decrease of fibrosis, radical alveolar counts and inhibition of the occurrence of epithelial-mesenchymal transition (EMT). Furthermore, MSCs+EPO co-treatment more significantly suppressed the levels of transforming growth factor-β1(TGF-β1) than MSCs or EPO alone. Collectively, these results suggested that MSCs, EPO in particular MSCs+EPO co-treatment could promote lung repair in hyperoxia-induced alveoli dysplasia injury via inhibition of TGF-β1 signaling pathway to further suppress EMT process and may be a promising therapeutic strategy.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsBronchopulmonary DysplasiaCells, CulturedCombined Modality TherapyDisease Models, AnimalEpithelial-Mesenchymal TransitionErythropoietinFemaleFibrosisHumansHyperoxiaMiceMice, Inbred C57BLPulmonary AlveoliRecombinant ProteinsEPO protein, humanErythropoietinRecombinant ProteinsTransforming Growth Factor beta1BPDEPOETMMSCsTGF-β1

Identifiers

PMID27191651
PMCPMC5216925
OpenAlexW2374696835

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.