Evidence map›Paper›PMID 27302634›Full record

ArticleCell proliferation2016

miRNA-34a promotes proliferation of human pulmonary artery smooth muscle cells by targeting PDGFRA.

Peng Wang, Jie Xu, Zhiling Hou, Fangfang Wang, Yingli Song, Jiao Wang, Hui Zhu, Hongbo Jin

Abstract read
In one paragraph

Article in Cell proliferation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. MicroRNAs and Heat Shock Proteins in Breast Cancer Biology.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  6. MicroRNA-34a: the bad guy in age-related vascular diseases.Cellular and molecular life sciences : CMLS · 2021
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

Peng WangDepartment of Physiology, College of Basic Medical Sciences, Harbin Medical University, Harbin, China.
Jie XuDepartment of Physiology, College of Basic Medical Sciences, Harbin Medical University, Harbin, China.
Zhiling HouDepartment of Emergency Surgery, The First Affiliated Hospital of Jiamusi University, Jiamusi, China.
Fangfang WangDepartment of Pathophysiology, College of Basic Medical Sciences, Jiamusi University, Jiamusi, China.
Yingli SongDepartment of Physiology, College of Basic Medical Sciences, Harbin Medical University, Harbin, China.
Jiao WangDepartment of Physiology, College of Basic Medical Sciences, Harbin Medical University, Harbin, China.
Hui ZhuDepartment of Physiology, College of Basic Medical Sciences, Harbin Medical University, Harbin, China.
Hongbo JinDepartment of Physiology, College of Basic Medical Sciences, Harbin Medical University, Harbin, China.
Harbin Medical University · CNJiamusi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPulmonary arterial hypertension (PAH) is a fast progressing vascular disease characterized by uncontrolled cell proliferation of pulmonary artery smooth muscle cells (PASMCs). Some studies have suggested that PAH and cancers share an apoptosis-resistant state, featuring excessive cell proliferation. The miR-34 family consists of tumour-suppressive miRNAs, and its reduced expression has been reported in numerous cancers; however, its role in hypoxia-induced PAH has not been previously studied. MATERIALS AND

methodsmiR-34 family expression was evaluated in a rat model with hypoxia and in cultured hypoxic PASMCs, using real-time quantitative PCR (RT-qPCR). Function of miR-34 family was assessed by transfecting miR-34 mimics and inhibitors. Dual luciferase reporter gene assays, RT-qPCR and Western blotting were performed to validate target genes of miR-34.

resultsSignificant down-regulation of miR-34a in hypoxic lung tissue, pulmonary artery and PASMCs was identified and then effects of miR-34a in modulating cell proliferation in human pulmonary artery smooth muscle cells (hPASMCs) was investigated in vitro. Reduction of miR-34a levels in hPASMCs caused increased proliferation and these effects were reversed by overexpression of miR-34a. miR-34a overexpression down-regulated platelet-derived growth factor receptor alpha (PDGFRA) expression, which is a key factor in PAH development. These results suggest that miR-34a is a potential regulator of proliferation in PASMCs, and that it could be used as a novel treatment strategy in PAH.

Indexed as

Cell ProliferationAnimalsApoptosisCell HypoxiaCell LineCyclin ACyclin EDNA DamageDown-RegulationHumansHypertension, PulmonaryHypoxiaLungMicroRNAsMyocytes, Smooth MuscleNerve Tissue ProteinsCyclin ACyclin EMicroRNAsMIRN34 microRNA, humanNerve Tissue ProteinsNFATC2 protein, humanNFATC Transcription FactorsPotassium Channels, Tandem Pore Domainpotassium channel subfamily K member 3Receptor, Platelet-Derived Growth Factor alpha

Identifiers

PMID27302634
PMCPMC6496014
OpenAlexW2427851148

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.