Evidence map›Paper›PMID 35638591›Full record

ArticleEuropean journal of histochemistry : EJH2022

MiR-130a-5p contributed to the progression of endothelial cell injury by regulating FAS.

Wei Wang, Wenbo Tang, Erbo Shan, Lei Zhang, Shiyuan Chen, Chaowen Yu, Yong Gao

Abstract read
In one paragraph

Article in European journal of histochemistry : EJH, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Noncoding RNAs as Key Regulators for Cardiac Development and Cardiovascular Diseases.Journal of cardiovascular development and disease · 2023
    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

7 authors.

Wei WangThe First Clinical College of Jinan University, Guangzhou, and Surgical Oncology Department, the Second Affiliated Hospital of Bengbu Medical College, Bengbu. wangwei@bbmc.edu.cn.
Wenbo TangVascular Surgery Department, the First Affiliated Hospital of Bengbu Medical College, Bengbu. twb0630@163.com.
Erbo ShanGeneral Surgery Department, the Second Affiliated Hospital of Bengbu Medical College, Bengbu. shanxiyi@126.com.
Lei ZhangSurgical Oncology Department, the Second Affiliated Hospital of Bengbu Medical College, Bengbu. leibyzl@163.com.
Shiyuan ChenVascular Surgery Department, the First Affiliated Hospital of Bengbu Medical College, Bengbu. 13309658851@189.cn.
Chaowen YuVascular Surgery Department, the First Affiliated Hospital of Bengbu Medical College, Bengbu. Doctoryu16@163.com.
Yong GaoThe First Clinical College of Jinan University, Guangzhou. 0000731@bbmc.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) play critical roles in the development of vascular diseases. However, the effects of miR-130a-5p and its functional targets on atherosclerosis (AS) are still largely unknown. In this regard, our aim is to explore the potentially important role of miR-130a-5p and its target gene during the progression of endothelial cell injury. We first found oxidized low-density lipoprotein (ox-LDL) induced FAS and cell apoptosis in HUVECs. Subsequently, miR-130a-5p expression was verified to be downregulated after ox-LDL treatment and negatively correlated with FAS, and FAS was identified as substantially upregulated in the ox-LDL-treated HUVEC cells. After that, the knockdown of FAS and overexpression of miR-130a-5p together were observed to aggregate ox-LDL-induced reduction of cell viability and apoptosis, cell cycle progression, cell proliferation, cell migration and invasion. In conclusion, we detected that miR-130a-5p contributed to the progression of endothelial cell injury by regulating of FAS, which may provide a new and promising therapeutic target for AS.

Indexed as

Atherosclerosisfas ReceptorMicroRNAsApoptosisCell MovementCell ProliferationHumansHuman Umbilical Vein Endothelial CellsScavenger Receptors, Class EFAS protein, humanfas ReceptorMicroRNAsMIRN130 microRNA, humanScavenger Receptors, Class E

Identifiers

PMID35638591
PMCPMC9201574

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.