Evidence map›Paper›PMID 32803651›Full record

ArticleMolecular and cellular biochemistry2020

LincRNA-Cox2 promotes pulmonary arterial hypertension by regulating the let-7a-mediated STAT3 signaling pathway.

Gesheng Cheng, Lu He, Yushun Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Review
  3. Roles of LncRNAs in the Pathogenesis of Pulmonary Hypertension.Reviews in cardiovascular medicine · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. A Novel Regulatory Player in the Innate Immune System: Long Non-Coding RNAs.International journal of molecular sciences · 2021
    Review
  11. Review
  12. Review
  13. Review
  14. 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

3 authors at 1 institution in 1 country.

Gesheng ChengDepartment of Structural Heart Disease, First Affiliated Hospital of Xi'an Jiaotong University, 277# West Yanta Road, Xi'an, 710061, Shaanxi, China.
Lu HeDepartment of Structural Heart Disease, First Affiliated Hospital of Xi'an Jiaotong University, 277# West Yanta Road, Xi'an, 710061, Shaanxi, China.
Yushun ZhangDepartment of Structural Heart Disease, First Affiliated Hospital of Xi'an Jiaotong University, 277# West Yanta Road, Xi'an, 710061, Shaanxi, China. 000501@xjtufh.edu.cn.ORCID http://orcid.org/0000-0003-4231-7471
First Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

the Natural Science Foundation of Shaanxi Province 20148JM7096
6 · The paper itself

Abstract

It is well supported by the literature that the proliferation and migration of pulmonary arterial smooth muscle cells (PASMCs) are critical for the development of pulmonary arterial hypertension (PAH). Long intergenic noncoding RNA COX2 (lincRNA-COX2) is a regulator of inflammation and might be conducive to the progression of atherosclerosis, while its role in PAH is still unclear. This study was performed to explore the role and mechanism of lincRNA-COX2 in PASMCs proliferation and migration in an anaerobic environment. PASMCs were treated by hypoxia to construct PAH cell models. RT-PCR and western blot were recruited to evaluate the expression levels of lincRNA-COX2, miR-let-7a and STAT3. Their roles in proliferation and cell and migration of PASMCs were determined by the CCK-8 assay, wound-healing assay, and flow cytometry. In peripheral blood samples from PAH patients and hypoxic PASMCs, lincRNA-COX2 expression was enhanced. Silencing lincRNA-COX2 inhibited hypoxia-induced PASMCs proliferation by influencing the G2/M phase of the cell cycle. Meanwhile, lincRNA-COX2 regulated STAT3 through miR-let-7a and its effects on hypoxic PASMCs worked through miR-let-7a/STAT3 axis. To conclude, silencing lincRNA-COX2 attenuated the development of hypoxic PASMCs. LincRNA-COX2/miR-let-7a/STAT3 axis might be considered as a novel target to treat PAH.

Indexed as

Cell ProliferationCells, CulturedHumansHypertension, PulmonaryHypoxiaMicroRNAsMyocytes, Smooth MusclePulmonary ArteryRNA, Long NoncodingSignal TransductionSTAT3 Transcription FactorMicroRNAsmirnlet7 microRNA, humanRNA, Long NoncodingSTAT3 protein, humanSTAT3 Transcription FactorLet-7aLinc-Cox2MigrationProliferationPulmonary arterial hypertensionSTAT3 signaling pathway

Identifiers

PMID32803651
OpenAlexW3049537892

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.