Evidence map›Paper›PMID 38656074›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2024

Integrative analyses of genetic characteristics associated with skeletal endothelial cells.

Zhanhui Wang, Bowen Hu, Xiaoming Chen, Zheng Zhang, Lu Liu, Nan Li, Chun Liang

Open access · goldAbstract read
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2024. 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
–field-weighted citation impact, top 93% 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, 0 citations in OpenAlex.

  1. 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

7 authors at 2 institutions in 1 country.

Zhanhui WangDepartment of Cardiology, Second Affiliated Hospital of Naval Medical University, Shanghai, China.ORCID http://orcid.org/0009-0001-1525-2804
Bowen HuDepartment of Cardiology, Second Affiliated Hospital of Naval Medical University, Shanghai, China.ORCID http://orcid.org/0000-0003-0908-4565
Xiaoming ChenDepartment I of Cadre's Ward, Navy 971st Hospital, Qingdao, China.ORCID http://orcid.org/0009-0007-6788-0726
Zheng ZhangDepartment of Orthopedic Rehabilitation, Qingdao Special Servicemen Recuperation Center of PLA Navy, Qingdao, China.ORCID http://orcid.org/0009-0005-0865-6690
Lu LiuDepartment I of Cadre's Ward, Navy 971st Hospital, Qingdao, China.ORCID http://orcid.org/0009-0002-8833-9924
Nan LiDepartment I of Cadre's Ward, Navy 971st Hospital, Qingdao, China.ORCID http://orcid.org/0009-0000-8028-731X
Chun LiangDepartment of Cardiology, Second Affiliated Hospital of Naval Medical University, Shanghai, China.ORCID http://orcid.org/0000-0002-4042-206X
PLA Navy General Hospital · CNPeople's Liberation Army 401 Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The osseous vascular endothelium encompasses a vast intricate framework that regulates bone remodeling. Osteoporosis, an age-associated systemic bone disease, is characterized by the degeneration of the vascular architecture. Nevertheless, the precise mechanisms underpinning the metamorphosis of endothelial cells (ECs) with advancing age remain predominantly enigmatic. In this study, we conducted a systematic analysis of differentially expressed genes (DEGs) and the associated pathways in juvenile and mature femoral ECs, utilizing data sourced from the Gene Expression Omnibus (GEO) repositories (GSE148804) and employing bioinformatics tools. Through this approach, we successfully discerned six pivotal genes, namely Adamts1, Adamts2, Adamts4, Adamts14, Col5a1, and Col5a2. Subsequently, we constructed a miRNA-mRNA network based on miRNAs displaying differential expression between CD31hiEMCNhi and CD31lowEMCNlow ECs, utilizing online repositories for prediction. The expression of miR-466i-3p and miR-466i-5p in bone marrow ECs exhibited an inverse correlation with age. Our in vivo experiments additionally unveiled miR-466i-5p as a pivotal regulator in osseous ECs and a promising therapeutic target for age-related osteoporosis.

Indexed as

Endothelial CellsMicroRNAsAnimalsGene Expression ProfilingHumansMiceOsteoporosisRNA, MessengerMicroRNAsRNA, Messenger

Identifiers

PMID38656074
PMCPMC11027181
OpenAlexW4394954712

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.