Evidence map›Paper›PMID 31934170›Full record

ArticleInternational journal of clinical and experimental pathology2019

High mobility group protein B1 (HMGB1) interacts with receptor for advanced glycation end products (RAGE) to promote airway smooth muscle cell proliferation through ERK and NF-

Dongming Qu, Zhougui Ling, Xiaoyu Tan, Yan Chen, Qinghua Huang, Mengze Li, Tangjuan Liu, Changchun Hou, Yiqiang Chen

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
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  11. International journal of molecular sciences · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Role of HMGB1 in Chemotherapy-Induced Peripheral Neuropathy.International journal of molecular sciences · 2020
    Review
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.

Dongming QuDepartment of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University Nanning 530021, China.
Zhougui LingDepartment of Respiratory and Critical Care Medicine, The Fourth Affiliated Hospital of Guangxi Medical University Liuzhou 545005, China.
Xiaoyu TanDepartment of Respiratory Medicine, The Second Affiliated Hospital of Guangxi Medical University Nanning 530021, China.
Yan ChenDepartment of Respiratory Medicine, The Second Affiliated Hospital of Guangxi Medical University Nanning 530021, China.
Qinghua HuangDepartment of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University Nanning 530021, China.
Mengze LiDepartment of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University Nanning 530021, China.
Tangjuan LiuDepartment of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University Nanning 530021, China.
Changchun HouDepartment of Respiratory Medicine, The Second Affiliated Hospital of Guangxi Medical University Nanning 530021, China.
Yiqiang ChenDepartment of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University Nanning 530021, China.
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh-mobility graoup box protein 1 (HMGB1) has been shown to mediate a wide range of pathologic responses by interacting with RAGE (receptor for advanced glycation endproducts) and TLRs (Toll-like receptors). Our previous study showed that HMGB1 has been involved in pathogenesis of airway remodeling in an allergen-induced chronic mice asthma model. Increased airway smooth muscle (ASM) mass is a vital feature of airway remodeling.

objectiveTo evaluate the effect of HMGB1 on proliferation of ASMs and the underlying mechanisms.

methodsRat airway smooth muscle cells (RASMs) were obtained by primary explant techniques. We investigated the effect of HMGB1 on the proliferation of RASMs. To identify which receptors and signaling pathways be involved in proliferation of RASMs, we performed western blot and CCK-8 assay by specific receptor blockade and inhibition of MAPK (p38, JNK and ERK) and NF-

resultsHMGB1 stimulated RASMs proliferation in a dose- and time-dependent manner and also increased proliferating cell nuclear antigen (PCNA) and RAGE expression of RASMs. The inhibitor of RAGE, but not TLR2 and TLR4, reversed HMGB1-induced RASM proliferation and PCNA expression. Incubation of RASMs with HMGB1 caused a rapid increase in P65 and ERK phosphorylation. RASM proliferation and PCNA expression toward HMGB1 were significantly inhibited by the inhibitors of ERK and NF-

conclusionHMGB1 induces proliferation of RASMs through a RAGE-dependent activation of ERK and NF-

Indexed as

cell remodelingHMGB1RAGERASM cells

Identifiers

PMID31934170
PMCPMC6949814
OpenAlexW3005880698

What OpenQuestion holds

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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.