Evidence map›Paper›PMID 42298877›Full record

ArticleGlobal spine journal2026

LncRNA NORAD Promotes Spinal Cord Injury via miR-22-3p/PTEN Axis to Regulate Oxidative Stress and Inflammation in Neuronal Cells.

Chenming Zhang, Lin Chen, Yue Pan, Shiwei Yu, Qingyi Wang, Yongfu Chen, Haitao Xu, Yuanyuan Zhang

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Article in Global spine journal, 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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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

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Chenming ZhangDepartment of Orthopedics, Tongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, China.
Lin ChenDepartment of Orthopedics, Jinjiang Anhai Hospital, Jinjiang, China.
Yue PanDepartment of Thoracic, Tongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, China.
Shiwei YuDepartment of Orthopedics, Tongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, China.
Qingyi WangKey Laboratory of Clinical Cohort Research on Bone and Joint Degenerative Diseases of Guangxi, Baise, China.
Yongfu ChenKey Laboratory of Clinical Cohort Research on Bone and Joint Degenerative Diseases of Guangxi, Baise, China.
Haitao XuDepartment of Orthopedics, Zhucheng People's Hospital, Weifang, China.ORCID 0009-0006-1657-5812
Yuanyuan ZhangDepartment of Hand and Foot Surgery Ward, Zibo Central Hospital, Zibo, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Study DesignRetrospective Study.ObjectiveSpinal cord injury (SCI) is a severe central nervous system trauma. To explore the regulatory mechanism of long non-coding RNA (lncRNA) NORAD in SCI.MethodsEighty healthy controls and 100 SCI patients were enrolled. Meanwhile, SCI animal models and LPS-induced cell models were established. Basso-Beattie-Bresnahan (BBB) scoring was performed to monitor hind-limb motor recovery. The NORAD biological function was evaluated through RT-qPCR, CCK-8 experiments, flow cytometry, enzyme-linked immunosorbent assay (ELISA), and the measurement of oxidative stress and metabolism-related indicators. The targeting relationships were verified through RIP experiments and dual-luciferase experiments.ResultsNORAD exhibited high expression in SCI patients and possessed good diagnostic utility for this disease. Its high expression may also be associated with the severity of injury. In SCI rats, inhibiting NORAD significantly improved the recovery of motor function and alleviated oxidative stress, cellular damage, and neuroinflammation, indicating a pro-injury role of NORAD during SCI pathogenesis. In addition, NORAD was highly expressed in the LPS-induced cell model, and promoted cellular damage, apoptosis, inflammatory responses, and oxidative stress by targeting and inhibiting miR-22-3p. While miR-22-3p directly targeted and inhibited PTEN, which was also highly expressed in the LPS-induced cell model. Functional rescue experiments further confirmed that the miR-22-3p inhibitor could reverse the protective effect of interfering with NORAD on SCI-related pathological damage, while silencing PTEN could offset the antagonistic effect of the miR-22-3p inhibitor, suggesting that the NORAD/miR-22-3p/PTEN axis constituted a positive feedback pro-injury loop.ConclusionsNORAD sequestered miR-22-3p to relieve PTEN repression and exacerbate SCI.

Indexed as

miR-22-3pNORADPTENspinal cord injury

Identifiers

PMID42298877
PMCPMC13272196

What Socratic holds

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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.