Evidence map›Paper›PMID 32709884›Full record

ArticleJournal of human hypertension2021

MiR-124-3p reduces angiotensin II-dependent hypertension by down-regulating EGR1.

Lingchun Lv, Jiayi Shen, Jian Xu, Xiaoyan Wu, Chunlai Zeng, Li Lin, Wei Mao, Tiemin Wei

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of human hypertension, 2021. 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
1.2field-weighted citation impact, top 23% 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, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The pharmaco-epigenetics of hypertension: a focus on microRNA.Molecular and cellular biochemistry · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

8 authors at 3 institutions in 1 country.

Lingchun Lv *Department of Cardiovascular Medicine, Lishui Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jiayi Shen *Department of Cardiovascular Medicine, Lishui Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jian XuDepartment of Cardiovascular Medicine, Lishui Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xiaoyan WuDepartment of Cardiovascular Medicine, Lishui Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Chunlai ZengDepartment of Cardiovascular Medicine, Lishui Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Li LinDepartment of Cardiovascular Medicine, Lishui Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Wei MaoDepartment of Cardiovascular Medicine, Zhejiang Traditional Chinese Medicine Hospital, Hangzhou, China. mowei_wma@163.com.ORCID http://orcid.org/0000-0002-5149-0682
Tiemin WeiDepartment of Cardiovascular Medicine, Lishui Hospital, Zhejiang University School of Medicine, Hangzhou, China. tmin_wei@163.com.
Lishui University · CNZhejiang Chinese Medical University · CNHangzhou Hospital of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Through previous literature studies, we found that miR-124-3p may be associated with hypertension. Therefore, we investigated the relationship between miR-124-3p and hypertension in Human Umbilical Vein Endothelial Cells (HUVECs) induced by angiotensin II (AngII). AngII-induced HUVECs model was constructed and the expression of miR-124-3p was detected by qRT-PCR. After transfected cells, apoptosis and ROS production were detected by flow cytometry, caspase-3 kit, and DCFH-DA staining. The target genes of miR-124-3p were predicted and verified by TargrtScan, Luciferase assay, qRT-PCR, and western blot. After silencing Early growth response factor 1 (siEGR1), its effects on apoptosis and ROS production were explored. Finally, the rescue experiments were conducted to explore the mechanism of miR-124-3p to reduce hypertension. MiR-124-3p was underexpressed in the cell model. In Ang II-induced HUVECs, the number of apoptosis increased, the content of caspase-3 was higher, and ROS production increased. However, these effects could be partially inhibited by miR-124-3p mimic. EGR1 was down-regulated by miR-124-3p, and siEGR1 was able to inhibit apoptosis and ROS production of cell model. In the final rescue experiments, miR-124-3p partially reversed the effect of Ang-II on the viability, migration, invasion and apoptosis and ROS production in HUVECs by down-regulating EGR1. MiR-124-3p inhibits Ang II-induced apoptosis and ROS production in HUVECs by down-regulating EGR1.

Indexed as

HypertensionMicroRNAsAngiotensin IIApoptosisEarly Growth Response Protein 1HumansHuman Umbilical Vein Endothelial CellsAngiotensin IIEarly Growth Response Protein 1EGR1 protein, humanMicroRNAsMIRN124 microRNA, human

Identifiers

PMID32709884
OpenAlexW3044229263

What Socratic 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 Socratic graph.