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啮齿动物急性脊髓损伤实验模型中的 miRNA 疗法:一项荟萃分析

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

作者信息

Wang Yang, Yi Hanxiao, Song Yancheng

机构信息

Department of Orthopedics, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangdong Pharmaceutical University, No. 19 Nonglinxia Road, Yuexiu District, Guangzhou, Guangdong Province, China.

Department of Radiotherapy, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, No. 600 Tianhe Road, Tianhe District, Guangzhou, Guangdong Province, China.

出版信息

Cell Mol Neurobiol. 2023 Apr;43(3):1147-1161. doi: 10.1007/s10571-022-01235-2. Epub 2022 Jun 1.

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.

摘要

微小RNA疗法在急性脊髓损伤(SCI)治疗方面受到广泛研究,为急性SCI的治疗提供了重要前景。我们旨在对微小RNA治疗SCI进行临床前验证。我们对EMBASE、PubMed、Web of Science、Cochrane图书馆和Scopus数据库进行了系统检索。在SCI模型中,接受微小RNA治疗的大鼠(使用最多的动物,占70%,n = 46篇文章)恢复显著[BBB评分,标准化均数差3.90,95%置信区间3.08 - 4.73,p < 0.01]。接受微小RNA治疗的SCI小鼠(占30%,n = 19篇文章)的前肢和后肢运动功能[握力,标准化均数差3.22,95%置信区间2.14 - 4.26;p < 0.01;BBB评分,标准化均数差3.47,95%置信区间2.38 - 4.56,p < 0.01;BMS评分,标准化均数差2.27,95%置信区间1.34 - 3.20,p < 0.01]也比对照组小鼠恢复得更好。然后,我们进行了亚组分析,发现高质量文章倾向于报道微小RNA的非治疗效果。此外,我们分析了46种微小RNA,包括9个微小RNA家族(miR - 21 - 5p/34a - 3p/124 - 3p/126 - 3p/223 - 3p/543 - 3p/30 - 3p/136 - 3p/15 - 5p),其中miR - 30 - 3p/136 - 3p/15 - 5p家族对大鼠运动功能恢复无效。总之,微小RNA是治疗SCI的有效药物,然而,合适的微小RNA载体以及哪种微小RNA对SCI最有效仍有待进一步研究。

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