miRNA-128 modulates bone neoplasms cells proliferation and migration through the WNT/β-catenin and EMT signal pathways

Abstract Background Bone neoplasms present poor prognosis due to recurrence and metastasis. Although the role microRNAs (miRNAs) in inhibiting growth and metastasis of bone neoplasms has been investigated, the underlying potential molecular mechanisms mediated by miRNA-128 (miR-218) for the invasive...

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Main Authors: Yang Li, Xiaotao Long, Ji Wang, Jing Peng, Kai Shen
Format: Article
Language:English
Published: BMC 2021-01-01
Series:Journal of Orthopaedic Surgery and Research
Subjects:
Online Access:https://doi.org/10.1186/s13018-020-02164-w
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author Yang Li
Xiaotao Long
Ji Wang
Jing Peng
Kai Shen
author_facet Yang Li
Xiaotao Long
Ji Wang
Jing Peng
Kai Shen
author_sort Yang Li
collection DOAJ
description Abstract Background Bone neoplasms present poor prognosis due to recurrence and metastasis. Although the role microRNAs (miRNAs) in inhibiting growth and metastasis of bone neoplasms has been investigated, the underlying potential molecular mechanisms mediated by miRNA-128 (miR-218) for the invasiveness of bone neoplasms cells are still not completely understood. The purpose of this study was to identify the regulatory mechanisms of miR-218 in bone neoplasms cells. Methods Western blotting, quantitative reverse transcription-polymerase chain reaction (qRT-PCR), Counting Kit-8 assay, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining, luciferase activity assay immunofluorescence, and immunohistochemistry were used to analyze the regulatory effects of miR-218 on bone neoplasms cells. Results Here, the results showed that transfection of miR-128 suppressed bone neoplasms cells proliferation, migration, and invasion. Genetic knockdown of miR-128 in bone neoplasms cells suppressed the activation of the Wnt/β-catenin and epithelial-mesenchymal transition (EMT) signaling pathways. Activation of Wnt or EMT blocked miR-128-inhibited cells proliferation and migration in bone neoplasms cells. Exogenously introduced miR-128 markedly inhibited tumor regeneration in bone neoplasms xenograft models. Conclusions These results define a tumor-regulated function for miR-128 in bone neoplasms by down-regulation of the Wnt/β-catenin and EMT signal pathways, which provided a potential target for bone neoplasms gene therapy.
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spelling doaj.art-19e72be8c2e74d1aae3570bbc3b4b0412022-12-22T04:20:45ZengBMCJournal of Orthopaedic Surgery and Research1749-799X2021-01-0116111010.1186/s13018-020-02164-wmiRNA-128 modulates bone neoplasms cells proliferation and migration through the WNT/β-catenin and EMT signal pathwaysYang Li0Xiaotao Long1Ji Wang2Jing Peng3Kai Shen4Department of Orthopedics, Chongqing General Hospital, University of the Chinese Academy of SciencesDepartment of Orthopedics, Chongqing General Hospital, University of the Chinese Academy of SciencesDepartment of Orthopedics, Chongqing General Hospital, University of the Chinese Academy of SciencesDepartment of Orthopedics, Chongqing General Hospital, University of the Chinese Academy of SciencesDepartment of Orthopedics, Chongqing General Hospital, University of the Chinese Academy of SciencesAbstract Background Bone neoplasms present poor prognosis due to recurrence and metastasis. Although the role microRNAs (miRNAs) in inhibiting growth and metastasis of bone neoplasms has been investigated, the underlying potential molecular mechanisms mediated by miRNA-128 (miR-218) for the invasiveness of bone neoplasms cells are still not completely understood. The purpose of this study was to identify the regulatory mechanisms of miR-218 in bone neoplasms cells. Methods Western blotting, quantitative reverse transcription-polymerase chain reaction (qRT-PCR), Counting Kit-8 assay, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining, luciferase activity assay immunofluorescence, and immunohistochemistry were used to analyze the regulatory effects of miR-218 on bone neoplasms cells. Results Here, the results showed that transfection of miR-128 suppressed bone neoplasms cells proliferation, migration, and invasion. Genetic knockdown of miR-128 in bone neoplasms cells suppressed the activation of the Wnt/β-catenin and epithelial-mesenchymal transition (EMT) signaling pathways. Activation of Wnt or EMT blocked miR-128-inhibited cells proliferation and migration in bone neoplasms cells. Exogenously introduced miR-128 markedly inhibited tumor regeneration in bone neoplasms xenograft models. Conclusions These results define a tumor-regulated function for miR-128 in bone neoplasms by down-regulation of the Wnt/β-catenin and EMT signal pathways, which provided a potential target for bone neoplasms gene therapy.https://doi.org/10.1186/s13018-020-02164-wmiRNA-128Bone neoplasmsProliferationMigrationWnt/β-cateninEMT
spellingShingle Yang Li
Xiaotao Long
Ji Wang
Jing Peng
Kai Shen
miRNA-128 modulates bone neoplasms cells proliferation and migration through the WNT/β-catenin and EMT signal pathways
Journal of Orthopaedic Surgery and Research
miRNA-128
Bone neoplasms
Proliferation
Migration
Wnt/β-catenin
EMT
title miRNA-128 modulates bone neoplasms cells proliferation and migration through the WNT/β-catenin and EMT signal pathways
title_full miRNA-128 modulates bone neoplasms cells proliferation and migration through the WNT/β-catenin and EMT signal pathways
title_fullStr miRNA-128 modulates bone neoplasms cells proliferation and migration through the WNT/β-catenin and EMT signal pathways
title_full_unstemmed miRNA-128 modulates bone neoplasms cells proliferation and migration through the WNT/β-catenin and EMT signal pathways
title_short miRNA-128 modulates bone neoplasms cells proliferation and migration through the WNT/β-catenin and EMT signal pathways
title_sort mirna 128 modulates bone neoplasms cells proliferation and migration through the wnt β catenin and emt signal pathways
topic miRNA-128
Bone neoplasms
Proliferation
Migration
Wnt/β-catenin
EMT
url https://doi.org/10.1186/s13018-020-02164-w
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