Evidence map›Paper›PMID 41021072›Full record

ArticleMolecular biology reports2025

Temporal dynamics and functional implications of MiRNAs in denervation-induced skeletal muscle atrophy.

Wei Li, Yuntian Shen, Hua Liu, Fei Xue, Jitai Zhang, Jia Yi, Xia Li, Leilei Gong, Xinlei Yao, Hualin Sun and 2 more

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Article in Molecular biology reports, 2025. 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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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

12 authors.

Wei Li *Department of Orthopedics, Affiliated Hospital of Nantong University, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China.
Yuntian Shen *Department of Orthopedics, Affiliated Hospital of Nantong University, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China.
Hua Liu *Department of Orthopedics, Haian Hospital of Traditional Chinese Medicine, Nantong, 226600, Jiangsu Province, People's Republic of China.
Fei XueDepartment of Orthopedics, Affiliated Hospital of Nantong University, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China.
Jitai ZhangDepartment of Orthopedics, Affiliated Hospital of Nantong University, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China.
Jia YiDepartment of Orthopedics, Affiliated Hospital of Nantong University, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China.
Xia LiDepartment of Orthopedics, Affiliated Hospital of Nantong University, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China.
Leilei GongDepartment of Orthopedics, Affiliated Hospital of Nantong University, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China.
Xinlei YaoDepartment of Orthopedics, Affiliated Hospital of Nantong University, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China.
Hualin SunDepartment of Orthopedics, Affiliated Hospital of Nantong University, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China.
Bingqian ChenDepartment of Orthopedics, Changshu Hospital Affiliated to Soochow University, First People's Hospital of Changshu City, Changshu, 215500, Jiangsu Province, People's Republic of China. cbq0433@suda.edu.cn.
Jianwei ZhuDepartment of Orthopedics, Affiliated Hospital of Nantong University, Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, 226001, Jiangsu Province, People's Republic of China. zhujianwei@ntu.edu.cn.

Funding

National Natural Science Foundation of China 82401633Suzhou Science and Technology Development Program SYW2024048
6 · The paper itself

Abstract

backgroundPeripheral nerve injury often leads to muscle atrophy and compromised functional recovery. Growing evidence underscores the critical role of microRNAs (miRNAs) as key epigenetic regulators in this degenerative process. However, most current studies are limited to isolated time points, leaving a gap in the systematic understanding of the temporal dynamics of miRNA expression and their regulatory networks during the initiation of muscle atrophy. METHODS AND

resultsIn this study, we employed small RNA sequencing to dynamically profile miRNA expression in the tibialis anterior muscle across a time series from 12 h to 28 days following denervation. Through differential expression analysis, functional enrichment, and construction of miRNA-mRNA interaction networks integrated with multi-dimensional bioinformatics approaches including GO and KEGG analyses, we identified 199 temporally differentially expressed miRNAs. A pronounced shift in miRNA expression was observed at day 3 post-injury. Functional annotation of target genes revealed an transition in regulatory emphasis from cytoskeletal remodeling toward energy metabolic imbalance. Within this core window of day 3, rno-miR-128-1-5p was found to regulate mitochondrial metabolism-related genes, and cooperated with rno-miR-296-3p in modulating tight junction pathways.

conclusionsOur findings illustrate that a time-specific molecular regulatory network underpins the pathological progression of denervation-induced muscle atrophy. These insights offer novel targets for developing precise therapeutic strategies aligned with disease timeline.

Indexed as

MicroRNAsMuscle, SkeletalMuscular AtrophyAnimalsComputational BiologyGene Expression ProfilingGene Expression RegulationGene Regulatory NetworksMaleMuscle DenervationMicroRNAsEnergy metabolismMiRNAMuscle atrophyPeripheral nerve injury

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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.