Evidence map›Paper›PMID 39154011›Full record

ArticleJournal of orthopaedic surgery and research2024

MiR-331-3p facilitates osteoporosis and may promote osteoporotic fractures by modulating NRP2 expression.

Cikedaoerji Na, Denggaowa Ao, Hongtao Chen

Abstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2024. 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
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Cikedaoerji NaSports Medicine Department of The Sixth Affiliated Hospital of Xinjiang Medical University, No.39, Wuxing South Road, Urumqi City, 830000, China.
Denggaowa AoOncology Department of The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830000, China.
Hongtao ChenSports Medicine Department of The Sixth Affiliated Hospital of Xinjiang Medical University, No.39, Wuxing South Road, Urumqi City, 830000, China. hongtaochen5632@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteoporosis (OP) is a high-incidence bone disease that is prone to osteoporotic fractures (OF), so it has attracted widespread attention.

aimThis study investigated the specific expression and role of miR-331 in patients with OP and OF. The findings have profound implications for the clinical prevention and treatment of these conditions.

methodsThe study included 60 OP patients, 46 OF patients, and 40 healthy controls. The expression level of miR-331-3p was detected using RT-qPCR. BMP2 was used to stimulate differentiation in MC3T3-E1 cells. After induction, the expression activity of osteogenic differentiation-related gene markers was detected using RT-qPCR. The target gene analysis was conducted using a luciferase reporter assay.

resultsThe levels of miR-331-3p were significantly elevated, while NRP2 levels were significantly reduced in OF patients. Post-surgery, miR-331-3p levels decreased over time. MiR-331-3p was found to negatively regulate the luciferase activity of NPR2 in MC3T3-E1 cells. Furthermore, overexpression of miR-331-3p inhibited cell proliferation and decreased the levels of osteoblast differentiation markers.

conclusionThe up-regulation of miR-331-3p can promote OP and might also encourage the occurrence of OF by regulating NRP2. However, this needs further verification.

Indexed as

MicroRNAsNeuropilin-2OsteoporosisOsteoporotic FracturesAgedAnimalsCell DifferentiationCell ProliferationFemaleGene ExpressionHumansMaleMiceMiddle AgedOsteoblastsOsteogenesisMicroRNAsMIRN331 microRNA, humanNeuropilin-2FractureMC3T3-E1miR-331-3pNPR2Osteoporosis

Identifiers

PMID39154011
PMCPMC11330005

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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.