Evidence map›Paper›PMID 37801489›Full record

ArticleBrazilian journal of cardiovascular surgery2023

Transcriptomics Provides Novel Insights into the Regulatory Mechanism of IncRNA HIF1 A-AS1 on Vascular Smooth Muscle Cells.

Jin Yang, Zhiqiang Gong, Junjie Dong, Haotian Li, Bing Wang, Kaili Du, Chunqiang Zhang, Lingqiang Chen

Open access · diamondAbstract read
In one paragraph

Article in Brazilian journal of cardiovascular surgery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Role of the lncRNA MALAT1/miR-1 Pathway in Mouse Myocardial Ischemia-Reperfusion Injury.Endocrine, metabolic & immune disorders drug targets · 2026
    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 1 institution in 1 country.

Jin YangDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Yunnan, People's Republic of China.
Zhiqiang GongDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Yunnan, People's Republic of China.
Junjie DongDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Yunnan, People's Republic of China.
Haotian LiDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Yunnan, People's Republic of China.
Bing WangDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Yunnan, People's Republic of China.
Kaili DuDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Yunnan, People's Republic of China.
Chunqiang ZhangDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Yunnan, People's Republic of China.
Lingqiang ChenDepartment of Orthopaedics, The First Affiliated Hospital of Kunming Medical University, Yunnan, People's Republic of China.
Kunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThoracic aortic aneurysm is a potentially fatal disease with a strong genetic contribution. The dysfunction of vascular smooth muscle cells (VSMCs) contributes to the formation of this aneurysm. Although previous studies suggested that long non-coding ribonucleic acid (RNA) hypoxia inducible factor 1 α-antisense RNA 1 (HIF1A-AS1) exerted a vital role in the progression and pathogenesis of thoracic aortic aneurysm, we managed to find a new regulatory mechanism of HIF1A-AS1 in VSMCs via transcriptomics.

methodsCell viability was detected by the cell counting kit-8 assay. Cell apoptosis was assessed by Annexin V-fluorescein isothiocyanate/propidium iodide double staining. Transwell migration assay and wound healing assay were performed to check the migration ability of HIF1A-AS1 on VSMCs. The NextSeq XTen system (Illumina) was used to collect RNA sequencing data. Lastly, reverse transcription-quantitative polymerase chain reaction confirmed the veracity and reliability of RNA-sequencing results.

resultsWe observed that overexpressing HIF1A-AS1 successfully promoted apoptosis, significantly altered cell cycle distribution, and greatly attenuated migration in VSMCs, further highlighting the robust promoting effects of HIF1A-AS1 to thoracic aortic aneurysm. Moreover, transcriptomics was implemented to uncover its underlying mechanism. A total of 175 differently expressed genes were identified, with some of them enriched in apoptosis, migration, and cell cycle-related pathways. Intriguingly, some differently expressed genes were noted in vascular development or coagulation function pathways.

conclusionWe suggest that HIF1A-AS1 mediated the progression of thoracic aortic aneurysm by not only regulating the function of VSMCs, but also altering vascular development or coagulation function.

Indexed as

Aortic Aneurysm, ThoracicRNA, Long NoncodingHumansMicroRNAsMuscle, Smooth, VascularMyocytes, Smooth MuscleReproducibility of ResultsTranscriptomeHIF1A-AS1 long non-coding RNA, humanMicroRNAsRNA, Long NoncodingApoptosisHypoxia Inducible Factor 1RNA Sequence AnalysisThoracic Aortic AneurysmVascular Smooth Muscle Cells

Identifiers

PMID37801489
PMCPMC10550220
OpenAlexW4387420724

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.