Evidence map›Paper›PMID 41275304›Full record

ArticleJournal of orthopaedic surgery and research2025

LINC00482 targets miR-877-3p to modulate osteogenic differentiation in fracture patients.

Hong Wang, Wei He

Abstract read
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Article in Journal of orthopaedic surgery and research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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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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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

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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

2 authors.

Hong WangThe First Clinical College of Guangzhou, University of Chinese Medicine, Guangzhou, 510405, China.
Wei HeThe First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine, No. 16, Airport Road, Guangzhou, 510405, China. Hewei_GZ16@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the diagnostic value of LINC00482 in patients with fractures and its regulatory role in osteogenic differentiation.

methodsA total of 194 participants were enrolled, of whom 103 had fractures. Fracture occurrence was determined via X-ray examination, and 5 mL of fasting venous blood was collected from all participants. Logistic regression analysis was employed to predict risk factors influencing fracture development. Receiver operating characteristic (ROC) curves assessed the diagnostic value of LINC00482 and miR-877-3p for fractures. RT-qPCR measured gene expression, while the CCK-8 assay evaluated cell proliferation. Dual luciferase reporter assays validated interactions between the target genes. Pearson correlation analysis examined the relationship between their expression relationship in fracture patients' serum.

resultsSerum from fracture patients exhibited significantly elevated LINC00482 levels and markedly reduced levels of miR-877-3p. Both demonstrated diagnostic value in predicting fracture occurrence. LINC00482, osteocalcin (OCN), and osteopontin (OPN) were identified as risk factors for fracture development. Transfection with si-LINC00482 promoted osteoblast proliferation and differentiation, and miR-877-3p was identified as a downstream target gene of LINC00482. The miR inhibitor reduced alkaline phosphatase (ALP) activity and inhibited osteoblast proliferation and differentiation.

conclusionLINC00482 may inhibit osteoblast proliferation and osteogenic differentiation by targeting miR-877-3p, thereby impeding fracture healing.

Indexed as

Cell DifferentiationFractures, BoneMicroRNAsRNA, Long NoncodingAdultAgedCell ProliferationCells, CulturedDown-RegulationFemaleHumansMaleMiddle AgedOsteoblastsOsteocalcinOsteogenesisBGLAP protein, humanMicroRNAsMIRN877 microRNA, humanOsteocalcinOsteopontinRNA, Long NoncodingSPP1 protein, humanDiagnosisFracture healingLINC00482miR-877-3pOsteogenic differentiation

Identifiers

PMID41275304
PMCPMC12751168

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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.