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皮肌炎和多发性肌炎肌肉中 miRNA 组学和 mRNA 组学的综合比较揭示了常见和特异的 miRNA-mRNAs。

Integrated comparison of the miRNAome and mRNAome in muscles of dermatomyositis and polymyositis reveals common and specific miRNA-mRNAs.

机构信息

Department of Rheumatology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha, Hunan 410008, PR China.

Department of Pathophysiology, Xiangya School of Medicine, Central South University, 87 Xiangya Road, Changsha, Hunan 410008, PR China.

出版信息

Epigenomics. 2019 Jan;11(1):23-33. doi: 10.2217/epi-2018-0064. Epub 2018 Dec 7.

Abstract

AIM

Dermatomyositis (DM) and polymyositis (PM) are refractory systemic autoimmune diseases with unknown pathogenesis. miRNAs is an important epigenetic mechanism to regulate gene expression.

METHODS

We performed whole miRNAs analysis, transcription analysis and the association between miRNAome and mRNAome.

RESULTS

For transcription and miRNAs analysis, there were common and specific mRNAs and miRNAs in the muscles of DM and PM. Among them, the expression levels of miR-196a-5p and CPM were negatively correlated in PM, miR-193b-3p and NECAP2 were negatively correlated in DM and PM. Protein carboxypeptidase M (CPM) plays roles in the degradation of extracellular proteins and in the migration and invasion of cancer cells, and protein NECAP2 plays roles in adaptor protein AP-1-mediated fast recycling from early endosomes. The functions of them in the pathogenesis of DM/PM need further studies.

CONCLUSION

Our study identified and confirmed differentially miRNAs and mRNAs in DM and PM. Our observations have laid the groundwork for further diagnostic and mechanistic studies of DM and PM.

摘要

目的

皮肌炎(DM)和多发性肌炎(PM)是难治性系统性自身免疫性疾病,其发病机制尚不清楚。miRNA 是一种重要的表观遗传机制,可调节基因表达。

方法

我们进行了全 miRNA 分析、转录分析以及 miRNA 组与 mRNA 组之间的关联分析。

结果

对于转录和 miRNA 分析,DM 和 PM 肌肉中存在共同和特异的 mRNAs 和 miRNAs。其中,CPM 和 miR-196a-5p 在 PM 中呈负相关,NECAP2 和 miR-193b-3p 在 DM 和 PM 中呈负相关。蛋白羧肽酶 M(CPM)在细胞外蛋白的降解和癌细胞的迁移和侵袭中发挥作用,蛋白 NECAP2 在衔接蛋白 AP-1 介导的早期内体快速回收中发挥作用。它们在 DM/PM 发病机制中的作用需要进一步研究。

结论

本研究鉴定并证实了 DM 和 PM 中差异表达的 miRNA 和 mRNAs。我们的观察结果为 DM 和 PM 的进一步诊断和机制研究奠定了基础。

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