Evidence map›Paper›PMID 25120760›Full record

ArticleInternational journal of clinical and experimental pathology2014

HMGB1 enhances smooth muscle cell proliferation and migration in pulmonary artery remodeling.

Huan-Liang Wang, Li-Ping Peng, Wen-Juan Chen, Shu-Hai Tang, Bao-Zhu Sun, Chun-Ling Wang, Rui Huang, Zhi-Jie Xu, Wei-Fu Lei

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

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  11. Blocking HMGB1 signal pathway protects early radiation-induced lung injury.International journal of clinical and experimental pathology · 2015
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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 1 institution in 1 country.

Huan-Liang WangDepartment of Anesthesiology, Qilu Hospital of Shandong University Jinan, Shandong, P.R. China.
Li-Ping PengDepartment of Anesthesiology, Qilu Hospital of Shandong University Jinan, Shandong, P.R. China.
Wen-Juan ChenDepartment of Anesthesiology, Qilu Hospital of Shandong University Jinan, Shandong, P.R. China.
Shu-Hai TangDepartment of Anesthesiology, Qilu Hospital of Shandong University Jinan, Shandong, P.R. China.
Bao-Zhu SunDepartment of Anesthesiology, Qilu Hospital of Shandong University Jinan, Shandong, P.R. China.
Chun-Ling WangDepartment of Anesthesiology, Qilu Hospital of Shandong University Jinan, Shandong, P.R. China.
Rui HuangDepartment of Anesthesiology, Qilu Hospital of Shandong University Jinan, Shandong, P.R. China.
Zhi-Jie XuDepartment of Anesthesiology, Qilu Hospital of Shandong University Jinan, Shandong, P.R. China.
Wei-Fu LeiDepartment of Anesthesiology, Qilu Hospital of Shandong University Jinan, Shandong, P.R. China.
Qilu Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HMGB1 is a necessary and critical mediator of acute lung injury and can act as a chemoattractant and anti-apoptosis factor in injury or repair in diseases. In this study we sought to determine whether HMGB1 is involved in the remodeling of pulmonary artery and investigate the mechanism. A rat model of pulmonary artery remodeling was successful induced with LPS infusion and the increasing of pulmonary arteries media was obviously inhibited in rats treated with thrice inject of HMGB1 neutralizing antibody. The percent of areas of tunica media to total artery wall was (0.53 ± 0.15), (0.81 ± 0.10) and (0.59 ± 0.11) in control, LPS and antibody group respectively (p<0.05). Meanwhile, treatment with HMGB1 neutralizing antibody not only decreased the level of HMGB1 mRNA and protein significantly, but inhibited the expression of PCAN and Bcl-2 as well. On the contrary, Bax, a gen which represented the apoptosis, revealed an absolutely reversed trend to Bcl-2 in pulmonary arteries. Experiments in vitro showed that HMGB1 could stimulate the proliferation of hPASMC in MTT test and increase the number of migrated cells in a concentration-dependent manner in chemotaxis assay using modified Boyden chambers. In conclusion, data from this study support the concept that HMGB1 is involved in the remodeling of pulmonary artery by enhancing proliferation and migration of smooth muscle cell. Inhibiting HMGB1 may be a new target to deal with the remodeling of pulmonary artery.

Indexed as

AnimalsBlotting, WesternCell LineCell MovementCell ProliferationDisease Models, AnimalHMGB1 ProteinHumansImmunohistochemistryIn Situ Nick-End LabelingMaleMuscle, Smooth, VascularMyocytes, Smooth MusclePulmonary ArteryRatsRats, WistarHMGB1 ProteinapoptosisHMGB1migrationproliferationpulmonary artery remodeling

Identifiers

PMID25120760
PMCPMC4128995
OpenAlexW2275537438

What OpenQuestion holds

Textmetadata
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.