在格雷夫眼病中非编码RNA介导的表观遗传变化:一个范围范围的系统性审查
Kourosh Shahraki1,2, Vida Ilkhani Pak1, Amin Najafi3
1Ocular Tissue Engineering Research Center, Ophthalmic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Non-coding RNA research
|June 16, 2023
概括
表观遗传过程,特别是microRNAs (miRNAs),在Graves眼病 (GO) 发病过程中发挥着作用. 需要进一步的研究来开发新的诊断和治疗工具GO.
科学领域:
- 眼科医生 眼科 眼科
- 遗传学 是一个遗传学.
- 免疫学 免疫学 免疫学
背景情况:
- 格雷夫斯眼病 (GO) 的发病可能涉及表观遗传机制.
- 专注于微RNAs (miRNAs),因为对它们在GO中的作用的研究有限.
研究的目的:
- 对非编码RNAs (ncRNAs),特别是miRNAs在GO病变发生中的作用进行范围审查.
- 为了识别GO的潜在miRNA生物标志物.
主要方法:
- 采用了六个阶段的方法框架和PRISMA指南.
- 在7个数据库中进行了全面的文献搜索,截至2022年2月.
- 对20个选定的文章进行了数据提取和定量/质量分析.
主要成果:
- 在GO中,ncRNAs参与调节炎症,T细胞功能,纤维化,葡萄糖皮质体敏感性,脂质积累,氧化应激和轨道纤维细胞增殖.
- 特定的miRNA如miR-146a,miR-21和miR-224-5p因其调节作用而被突出.
- 11个miRNA被确定为GO的潜在生物标志物.
结论:
- 显著的证据将ncRNA介导的表观遗传功能障碍与GO联系起来.
- 需要进一步的研究才能充分理解这些表观遗传联系.
- 这种理解可以导致对GO的新型诊断,预后和治疗策略.
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