Evidence map›Paper›PMID 39192334›Full record

ArticleJournal of orthopaedic surgery and research2024

Functional mechanism and clinical implications of LINC00339 in delayed fracture healing.

Yuntao Li, Ya Sun, Ke Ma, Shengqian Wang, Zhibiao Wang, Lina Huang

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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Article
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  3. let-7c-5p promotes fracture healing by downregulating CDK8.Journal of orthopaedic surgery and research · 2026
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  4. Article
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  9. LINC00341 promotes fracture healing through downregulation of miR-133a-3p.Journal of orthopaedic surgery and research · 2025
    Article
  10. Article
  11. MiR-376a-3p inhibits bone repair by regulating osteoblastic differentiation.Journal of orthopaedic surgery and research · 2025
    Article
  12. Article
  13. MiR-148a-3p regulates the fracture healing process by targeting MAFB.Journal of orthopaedic surgery and research · 2025
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  14. Article
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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

6 authors.

Yuntao Li *Department of Integrated Traditional Chinese and Western Medicine, Tianjin Hospital, Tianjin, 300211, China.
Ya Sun *Department of Breast Oncology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China.
Ke MaCollege of Medical Technology, Zibo Vocational Institute, Zibo, 255000, China.
Shengqian WangDepartment of Emergency, Zibo Combined Traditional Chinese and Western Medicine Hospital, Zibo, 255000, China.
Zhibiao WangDepartment of Orthopedics, Rizhao Central Hospital, No. 66, Wanghai Road, Donggang District, Rizhao City, Shandong Province, 276800, China. wangzhibo53@163.com.
Lina HuangDepartment of Rehabilitation Medicine, The Affiliated Hospital of Youjiang Medical University for Nationalities, No.18, Zhongshan 2nd Road, Youjiang District, Baise City, Guangxi, 533000, China. 14736050709@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDelayed fracture healing is a common complication of fractures that significantly impacts human health. This study aimed to explore the role of LINC00339 (lncRNA) in delayed fracture healing to provide new directions for its treatment.

methodsThis study included 82 patients with fractures healing in a normal manner and 90 patients experiencing delayed fracture healing. Levels of LINC00339, miR-16-5p, and osteogenic marker-related mRNAs were measured using RT-qPCR. The predictive potential of LINC00339 for delayed fracture healing was validated using ROC curve analysis. The interaction between LINC00339 and miR-16-5p was validated using dual-luciferase reporter assays and RIP experiments. CCK-8 was used to assess cell proliferation, and apoptosis rates were measured by flow cytometry.

resultsLINC00339 was significantly upregulated in delayed fracture healing patients and exhibited strong predictive ability for this condition. Overexpression of LINC00339 inhibited osteoblast proliferation, promoted apoptosis, and reduced mRNA levels of osteogenic markers (P < 0.05). miR-16-5p was recognized as a target mRNA of LINC00339, with LINC00339 exerting negative regulation on miR-16-5p, while overexpression of miR-16-5p mitigated the inhibitory effects of LINC00339 on fracture healing (P < 0.05).

conclusionThis research indicated that LINC00339 may serve as a diagnostic marker for delayed fracture healing and revealed the function of the LINC00339/miR-16-5p axis on fracture healing by regulating osteoblasts.

Indexed as

ApoptosisCell ProliferationFracture HealingMicroRNAsRNA, Long NoncodingAdultCells, CulturedFemaleHumansMaleMiddle AgedOsteoblastsOsteogenesisUp-RegulationLINC00339 long noncoding RNA, humanMicroRNAsMIRN16 microRNA, humanRNA, Long NoncodingDelayed fracture healingLINC00339miR-16-5pOsteoblast

Identifiers

PMID39192334
PMCPMC11348643

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.