Evidence map›Paper›PMID 29287621›Full record

ArticleEBioMedicine2018

Glucocorticoids Regulate the Vascular Remodeling of Aortic Dissection Via the p38 MAPK-HSP27 Pathway Mediated by Soluble TNF-RII.

Lei Zhang, Jian Zhou, Zaiping Jing, Yu Xiao, Yudong Sun, Yani Wu, Huiying Sun

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
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  3. Review
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  5. Article
  6. Review
  7. ALDHBMC cardiovascular disorders · 2022
    Article
  8. Article
  9. Article
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  11. Review
  12. Article
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  14. Article
  15. Article
  16. The Role of Macrophages in Aortic Dissection.Frontiers in physiology · 2020
    Review
  17. 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 2 institutions in 1 country.

Lei ZhangDepartment of Vascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
Jian ZhouDepartment of Vascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China. Electronic address: zhoujian1-2@163.com.
Zaiping JingDepartment of Vascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China. Electronic address: xueguanky@163.com.
Yu XiaoDepartment of Vascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
Yudong SunDepartment of Vascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
Yani WuDepartment of Breast and Thyroid Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
Huiying SunDepartment of Vascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
Changhai Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing researches suggest that inflammatory response is involved in vascular remodeling, which plays an important role in the development of aortic dissection. Glucocorticoids have been widely used in the clinical practice due to its powerful and effective anti-inflammatory property. However, the potential relationship between glucocorticoids and aortic dissection was still obscure. This study sought to elucidate the effect of glucocorticoids on the development and progression of aortic dissection, and the potential mechanism involved. Serum cortisol in aortic dissection patients was significantly higher than that in non-ruptured aortic aneurysm patients and healthy volunteers by radioimmunoassay. In modified C57BL/6 mouse model of aortic dissection, glucocorticoids reduced the incidence of aortic dissection and protected the collagen from degradation. Furthermore, glucocorticoids inhibited the TNF-α secretion of THP-1 monocytes, decreased the migration, phenotype switch from contractile type to synthetic type, and the apoptosis of human aortic smooth muscle cells induced by TNF-α. Finally, TNF-sRII was identified as an important cytokine in cellular interaction that participated in vascular remodeling by targeting the p38 MAPK-HSP27 pathway. These results indicate that glucocorticoids inhibit the incidence of aortic dissection by decreasing the TNF-α secretion and increasing the uncombined TNF-sRII, positively participating in vascular remodeling.

Indexed as

Signal TransductionAdrenocorticotropic HormoneAnimalsAortic DissectionCell LineCell MovementCoculture TechniquesCollagenDisease Models, AnimalGlucocorticoidsHSP27 Heat-Shock ProteinsHumansHydrocortisoneMacrophage ActivationMice, Inbred C57BLMyocytes, Smooth MuscleAdrenocorticotropic HormoneCollagenGlucocorticoidsHSP27 Heat-Shock ProteinsHydrocortisonep38 Mitogen-Activated Protein KinasesReceptors, GlucocorticoidReceptors, Tumor Necrosis Factor, Type IIAortic dissectionGlucocorticoidSoluble TNF-RIITNF-αVascular remodeling

Identifiers

PMID29287621
PMCPMC5828293
OpenAlexW2771773353

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.