The role and regulatory mechanism of miR-122-5p in the process of pilon fracture healing

Abstract Objective To explore the role and mechanism of miR-122-5p in the process of fracture healing following a Pilon fracture, as well as to further assess the clinical significance of this molecule as a potential diagnostic marker for fracture nonunion. Methods The expression levels of miR-122-5...

Full description

Saved in:
Bibliographic Details
Main Authors: Yang Zhang, Yingnan Li, Min Zhou, Lichang Yang
Format: Article
Language:English
Published: BMC 2025-07-01
Series:Journal of Orthopaedic Surgery and Research
Subjects:
Online Access:https://doi.org/10.1186/s13018-025-06120-4
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849332392451375104
author Yang Zhang
Yingnan Li
Min Zhou
Lichang Yang
author_facet Yang Zhang
Yingnan Li
Min Zhou
Lichang Yang
author_sort Yang Zhang
collection DOAJ
description Abstract Objective To explore the role and mechanism of miR-122-5p in the process of fracture healing following a Pilon fracture, as well as to further assess the clinical significance of this molecule as a potential diagnostic marker for fracture nonunion. Methods The expression levels of miR-122-5p were examined in patients with Pilon fracture healed and nonunion, respectively. ROC analysis was employed to evaluate the diagnostic value of miR-122-5p in identifying fracture nonunion, while logistic regression identified its risk factors. The effects of miR-122-5p on the proliferation, apoptosis, and osteogenic differentiation markers of osteoblasts were analyzed by CCK-8 assays, flow cytometry, RT-qPCR, and ALP assay kit. Additionally, DLR and RIP assays validated miR-122-5p targeting PDCD4. Results Serum miR-122-5p was significantly under-expressed in patients with fracture nonunion, whereas PDCD4 exhibits a notable over-expressed. Serum miR-122-5p can predict non-union of fractures, with a sensitivity of 90.82% and a specificity of 78.33%. Low miR-122-5p expression is a potential risk factor for fracture nonunion. The overexpression of miR-122-5p enhanced the proliferation ability of osteoblasts, inhibited cell apoptosis, and upregulated the expressions of ALP, OCN, and RUNX2; knockdown of miR-122-5p elicits opposite effect. PDCD4 is a direct target of miR-122-5p. The osteoblast dysfunction induced by miR-122-5p inhibitors can be reversed by down-regulating PDCD4. Conclusion Diminished miR-122-5p emerge as a potential prognostic indicator for nonunion in Pilon fractures. miR-122-5p accelerates the healing of Pilon fractures by targeting and inhibiting PDCD4.
format Article
id doaj-art-a4f898deb285413083b5d9b1db661a6d
institution Kabale University
issn 1749-799X
language English
publishDate 2025-07-01
publisher BMC
record_format Article
series Journal of Orthopaedic Surgery and Research
spelling doaj-art-a4f898deb285413083b5d9b1db661a6d2025-08-20T03:46:12ZengBMCJournal of Orthopaedic Surgery and Research1749-799X2025-07-012011910.1186/s13018-025-06120-4The role and regulatory mechanism of miR-122-5p in the process of pilon fracture healingYang Zhang0Yingnan Li1Min Zhou2Lichang Yang3Faculty of Life science and Technology, Kunming University of Science and TechnologyFaculty of Life science and Technology, Kunming University of Science and TechnologyDepartment of Orthopedics and Traumatology, Wuxi Second Hospital of Traditional Chinese MedicineGraduate School, Nanjing University of Chinese MedicineAbstract Objective To explore the role and mechanism of miR-122-5p in the process of fracture healing following a Pilon fracture, as well as to further assess the clinical significance of this molecule as a potential diagnostic marker for fracture nonunion. Methods The expression levels of miR-122-5p were examined in patients with Pilon fracture healed and nonunion, respectively. ROC analysis was employed to evaluate the diagnostic value of miR-122-5p in identifying fracture nonunion, while logistic regression identified its risk factors. The effects of miR-122-5p on the proliferation, apoptosis, and osteogenic differentiation markers of osteoblasts were analyzed by CCK-8 assays, flow cytometry, RT-qPCR, and ALP assay kit. Additionally, DLR and RIP assays validated miR-122-5p targeting PDCD4. Results Serum miR-122-5p was significantly under-expressed in patients with fracture nonunion, whereas PDCD4 exhibits a notable over-expressed. Serum miR-122-5p can predict non-union of fractures, with a sensitivity of 90.82% and a specificity of 78.33%. Low miR-122-5p expression is a potential risk factor for fracture nonunion. The overexpression of miR-122-5p enhanced the proliferation ability of osteoblasts, inhibited cell apoptosis, and upregulated the expressions of ALP, OCN, and RUNX2; knockdown of miR-122-5p elicits opposite effect. PDCD4 is a direct target of miR-122-5p. The osteoblast dysfunction induced by miR-122-5p inhibitors can be reversed by down-regulating PDCD4. Conclusion Diminished miR-122-5p emerge as a potential prognostic indicator for nonunion in Pilon fractures. miR-122-5p accelerates the healing of Pilon fractures by targeting and inhibiting PDCD4.https://doi.org/10.1186/s13018-025-06120-4miR-122-5pPDCD4Pilon fracturesFracture healingOsteoblasts
spellingShingle Yang Zhang
Yingnan Li
Min Zhou
Lichang Yang
The role and regulatory mechanism of miR-122-5p in the process of pilon fracture healing
Journal of Orthopaedic Surgery and Research
miR-122-5p
PDCD4
Pilon fractures
Fracture healing
Osteoblasts
title The role and regulatory mechanism of miR-122-5p in the process of pilon fracture healing
title_full The role and regulatory mechanism of miR-122-5p in the process of pilon fracture healing
title_fullStr The role and regulatory mechanism of miR-122-5p in the process of pilon fracture healing
title_full_unstemmed The role and regulatory mechanism of miR-122-5p in the process of pilon fracture healing
title_short The role and regulatory mechanism of miR-122-5p in the process of pilon fracture healing
title_sort role and regulatory mechanism of mir 122 5p in the process of pilon fracture healing
topic miR-122-5p
PDCD4
Pilon fractures
Fracture healing
Osteoblasts
url https://doi.org/10.1186/s13018-025-06120-4
work_keys_str_mv AT yangzhang theroleandregulatorymechanismofmir1225pintheprocessofpilonfracturehealing
AT yingnanli theroleandregulatorymechanismofmir1225pintheprocessofpilonfracturehealing
AT minzhou theroleandregulatorymechanismofmir1225pintheprocessofpilonfracturehealing
AT lichangyang theroleandregulatorymechanismofmir1225pintheprocessofpilonfracturehealing
AT yangzhang roleandregulatorymechanismofmir1225pintheprocessofpilonfracturehealing
AT yingnanli roleandregulatorymechanismofmir1225pintheprocessofpilonfracturehealing
AT minzhou roleandregulatorymechanismofmir1225pintheprocessofpilonfracturehealing
AT lichangyang roleandregulatorymechanismofmir1225pintheprocessofpilonfracturehealing