Literature DB >> 35648313

miRNA Therapy in Laboratory Models of Acute Spinal Cord Injury in Rodents: A Meta-analysis.

Yang Wang1, Hanxiao Yi2, Yancheng Song3.   

Abstract

miRNA therapy is popularly investigated in treating acute spinal cord injury (SCI) and offers a significant prospect for the treatment of acute SCI. We aimed to provide pre-clinical validations of miRNA in the treatment of SCI. A systematic search of EMBASE, PubMed, Web of Science, the Cochrane Library, and Scopus databases was performed. Rats, which were the most used animals (70%, n = 46 articles), receiving miRNA therapy got prominent recovery in SCI models [BBB score, SMD 3.90, 95% CI 3.08-4.73, p < 0.01]. Locomotor function of fore and hind limbs in SCI mice receiving miRNA therapy (30%, n = 19 articles) [grip strength, SMD 3.22, 95% CI 2.14-4.26; p < 0.01; BBB score, SMD 3.47, 95% CI 2.38-4.56, p < 0.01; BMS, SMD 2.27, 95% CI 1.34-3.20, p < 0.01] also recovered better than mice in control group. Then, we conducted the subgroup analysis and did find that high-quality articles trended to report non-therapeutic effect of miRNA. Furtherly, we analyzed 46 miRNAs, including 9 miRNA families (miR-21-5p/34a-3p/124-3p/126-3p/223-3p/543-3p/30-3p/136-3p/15-5p), among which miR-30-3p/136-3p/15-5p family were not effective in recovering locomotor function of rats. Conclusively, miRNAs are curative drugs for SCI, however, appropriate miRNA carrier and which miRNA is the most efficacious for SCI should be furtherly investigated.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Acute spinal cord injury; Locomotor function; Meta-analysis; Pre-clinical validations; Rodents; miRNA therapy

Year:  2022        PMID: 35648313     DOI: 10.1007/s10571-022-01235-2

Source DB:  PubMed          Journal:  Cell Mol Neurobiol        ISSN: 0272-4340            Impact factor:   5.046


  41 in total

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3.  Exosomes Derived from miR-126-modified MSCs Promote Angiogenesis and Neurogenesis and Attenuate Apoptosis after Spinal Cord Injury in Rats.

Authors:  Jiang-Hu Huang; Yang Xu; Xiao-Ming Yin; Fei-Yue Lin
Journal:  Neuroscience       Date:  2019-11-06       Impact factor: 3.590

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Journal:  Sheng Li Xue Bao       Date:  2017-12-25

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Journal:  Eur Rev Med Pharmacol Sci       Date:  2018-02       Impact factor: 3.507

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Journal:  Brain       Date:  2012-03-30       Impact factor: 13.501

8.  MicroRNA-362-3p attenuates motor deficit following spinal cord injury via targeting paired box gene 2.

Authors:  Yaguang Hu; Qian Liu; Min Zhang; Yousheng Yan; Hongmei Yu; Li Ge
Journal:  J Integr Neurosci       Date:  2019-03-30       Impact factor: 2.117

9.  MicroRNA-127 targeting of mitoNEET inhibits neurite outgrowth, induces cell apoptosis and contributes to physiological dysfunction after spinal cord transection.

Authors:  Qin-Qin He; Liu-Lin Xiong; Fei Liu; Xiang He; Guo-Ying Feng; Fei-Fei Shang; Qing-Jie Xia; You-Cui Wang; De-Lu Qiu; Chao-Zhi Luo; Jia Liu; Ting-Hua Wang
Journal:  Sci Rep       Date:  2016-10-17       Impact factor: 4.379

10.  Neuron-derived exosomes-transmitted miR-124-3p protect traumatically injured spinal cord by suppressing the activation of neurotoxic microglia and astrocytes.

Authors:  Dongdong Jiang; Fangyi Gong; Xuhui Ge; Chengtang Lv; Chenyu Huang; Shuang Feng; Zheng Zhou; Yuluo Rong; Jiaxing Wang; Chengyue Ji; Jian Chen; Wene Zhao; Jin Fan; Wei Liu; Weihua Cai
Journal:  J Nanobiotechnology       Date:  2020-07-25       Impact factor: 10.435

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