Evidence mapPaperPMID 42067916Full record

ArticleHereditas2026

Diagnostic value of LncRNA JPX in osteoporotic fracture (OPF) and its role in inhibiting osteogenic differentiation by targeting miR-219a-5p.

Junli Li, Yiwei Li, Ningning Zhang, Zhijian Cheng

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Article in Hereditas, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Junli LiEndocrinology and Metabolic Diseases Department, Yantai Yantaishan Hospital, Yantai, 264003, China.
Yiwei LiDepartment of Orthopedics, Pan'an People's Hospital, Pan'an, 322300, China.
Ningning ZhangDepartment of Orthopedics, Affiliated Hospital of Hebei University of Engineering, Handan, 056000, China.
Zhijian ChengDepartment of Orthopedics, The Second Affiliated Hospital of Xi'an Jiaotong University, No. 157, West Fifth Road, Xi'an, 710004, China. Drchengzj157@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study was designed to investigate the diagnostic potential of the long non-coding RNA JPX in osteoporotic fractures (OPF) and to explore its functional role in the regulation of fracture healing.

methodsA total of 244 patients with osteoporosis were enrolled, including 110 with osteoporosis (OP) and 134 with OPF. Expression levels of JPX, miR-219a-5p, and osteogenic markers (OPG, ALP, Collagen I, OCN) were detected by RT-qPCR. ROC analysis was employed to assess the clinical value of JPX. In human bone marrow mesenchymal stem cells (hBMSCs), gain- and loss-of-function experiments were performed to modulate JPX and miR-219a-5p expression. Cell proliferation was evaluated by CCK-8 assay. Flow cytometry assessed apoptosis. Dual luciferase reporter assays and RIP experiments validated the targeting relationship between JPX and miR-219a-5p.

resultsJPX was upregulated in the OPF group, with good diagnostic performance (AUC = 0.897; specificity = 76.87%; sensitivity = 84.55%), and JPX was identified an independent predictive factor. DFH and NFH could also be distinguished. JPX upregulation inhibited proliferation, promoted apoptosis, and suppressed osteogenic markers and ALP activity. JPX largely resides in the cytoplasm and directly binds miR-219a-5p, forming a ceRNA axis; upregulation of miR-219a-5p could reverse these effects.

conclusionJPX is associated with fracture risk and delayed healing, potentially influencing osteogenesis by sponge-like regulation of miR-219a-5p.

Indexed as

Cell DifferentiationMicroRNAsOsteogenesisOsteoporotic FracturesRNA, Long NoncodingAgedApoptosisBiomarkersCell ProliferationFemaleHumansMaleMesenchymal Stem CellsMiddle AgedBiomarkersMicroRNAsMIRN219 microRNA, humanRNA, Long NoncodingFracture healingJPXmiR-219a-5pOsteoporotic fractures

Identifiers

PMID42067916
PMCPMC13289444

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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 Socratic graph.